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- [1] Use of prenatal exome sequencing in fetuses with ultrasound anomalies[J]. EUROPEAN JOURNAL OF HUMAN GENETICS, 2023, 31 : 364 - 364Segura-Puimedon, Maria论文数: 0 引用数: 0 h-index: 0机构: qGenomics, NGS Clin Dept, Esplugas de Llobregat, Spain qGenomics, NGS Clin Dept, Esplugas de Llobregat, SpainCarreno, Marta论文数: 0 引用数: 0 h-index: 0机构: qGenomics, NGS Clin Dept, Esplugas de Llobregat, Spain qGenomics, NGS Clin Dept, Esplugas de Llobregat, SpainGarcia, Raquel论文数: 0 引用数: 0 h-index: 0机构: qGenomics, NGS Clin Dept, Esplugas de Llobregat, Spain qGenomics, NGS Clin Dept, Esplugas de Llobregat, SpainCarreno, Lidia论文数: 0 引用数: 0 h-index: 0机构: qGenomics, NGS Clin Dept, Esplugas de Llobregat, Spain qGenomics, NGS Clin Dept, Esplugas de Llobregat, SpainSan Nicolas, Hector论文数: 0 引用数: 0 h-index: 0机构: qGenomics, NGS Clin Dept, Esplugas de Llobregat, Spain qGenomics, NGS Clin Dept, Esplugas de Llobregat, SpainArjona, Cesar论文数: 0 引用数: 0 h-index: 0机构: qGenomics, NGS Clin Dept, Esplugas de Llobregat, Spain qGenomics, NGS Clin Dept, Esplugas de Llobregat, SpainSintas, Celia论文数: 0 引用数: 0 h-index: 0机构: qGenomics, NGS Clin Dept, Esplugas de Llobregat, Spain qGenomics, NGS Clin Dept, Esplugas de Llobregat, SpainVilla Marcos, Olaya论文数: 0 引用数: 0 h-index: 0机构: qGenomics, NGS Clin Dept, Esplugas de Llobregat, Spain qGenomics, NGS Clin Dept, Esplugas de Llobregat, SpainVinas-Jornet, Marina论文数: 0 引用数: 0 h-index: 0机构: qGenomics, NGS Clin Dept, Esplugas de Llobregat, Spain qGenomics, NGS Clin Dept, Esplugas de Llobregat, SpainVall, Monica论文数: 0 引用数: 0 h-index: 0机构: qGenomics, NGS Clin Dept, Esplugas de Llobregat, Spain qGenomics, NGS Clin Dept, Esplugas de Llobregat, SpainBosch, Nina论文数: 0 引用数: 0 h-index: 0机构: qGenomics, NGS Clin Dept, Esplugas de Llobregat, Spain qGenomics, NGS Clin Dept, Esplugas de Llobregat, SpainArmengol, Lluis论文数: 0 引用数: 0 h-index: 0机构: qGenomics, NGS Clin Dept, Esplugas de Llobregat, Spain qGenomics, NGS Clin Dept, Esplugas de Llobregat, Spain
- [2] Use of prenatal exome sequencing in fetuses with ultrasound anomalies[J]. EUROPEAN JOURNAL OF HUMAN GENETICS, 2020, 28 (SUPPL 1) : 150 - 151Segura-Puimedon, M.论文数: 0 引用数: 0 h-index: 0机构: qGenomics, Quantitat Genom Med Labs, Barcelona, Spain qGenomics, Quantitat Genom Med Labs, Barcelona, SpainCampos, B.论文数: 0 引用数: 0 h-index: 0机构: qGenomics, Quantitat Genom Med Labs, Barcelona, Spain qGenomics, Quantitat Genom Med Labs, Barcelona, SpainLuna, J.论文数: 0 引用数: 0 h-index: 0机构: qGenomics, Quantitat Genom Med Labs, Barcelona, Spain qGenomics, Quantitat Genom Med Labs, Barcelona, SpainSintas, C.论文数: 0 引用数: 0 h-index: 0机构: qGenomics, Quantitat Genom Med Labs, Barcelona, Spain qGenomics, Quantitat Genom Med Labs, Barcelona, Spainde Castro-Miro, M.论文数: 0 引用数: 0 h-index: 0机构: qGenomics, Quantitat Genom Med Labs, Barcelona, Spain qGenomics, Quantitat Genom Med Labs, Barcelona, SpainDiez, H.论文数: 0 引用数: 0 h-index: 0机构: qGenomics, Quantitat Genom Med Labs, Barcelona, Spain qGenomics, Quantitat Genom Med Labs, Barcelona, SpainEstruch, S. B.论文数: 0 引用数: 0 h-index: 0机构: qGenomics, Quantitat Genom Med Labs, Barcelona, Spain qGenomics, Quantitat Genom Med Labs, Barcelona, SpainGarcia, R.论文数: 0 引用数: 0 h-index: 0机构: qGenomics, Quantitat Genom Med Labs, Barcelona, Spain qGenomics, Quantitat Genom Med Labs, Barcelona, SpainQuintana, L.论文数: 0 引用数: 0 h-index: 0机构: qGenomics, Quantitat Genom Med Labs, Barcelona, Spain qGenomics, Quantitat Genom Med Labs, Barcelona, SpainRodriguez, J.论文数: 0 引用数: 0 h-index: 0机构: qGenomics, Quantitat Genom Med Labs, Barcelona, Spain qGenomics, Quantitat Genom Med Labs, Barcelona, SpainArmengol, L.论文数: 0 引用数: 0 h-index: 0机构: qGenomics, Quantitat Genom Med Labs, Barcelona, Spain qGenomics, Quantitat Genom Med Labs, Barcelona, Spain
- [3] The diagnostic yield of prenatal exome sequencing in fetuses with ultrasound anomalies[J]. EUROPEAN JOURNAL OF HUMAN GENETICS, 2023, 31 : 364 - 364Diderich, Karin论文数: 0 引用数: 0 h-index: 0机构: Erasmus MC, Clin Genet, Rotterdam, Netherlands Erasmus MC, Clin Genet, Rotterdam, NetherlandsThurik, Florentine论文数: 0 引用数: 0 h-index: 0机构: Erasmus MC, Clin Genet, Rotterdam, Netherlands Erasmus MC, Clin Genet, Rotterdam, NetherlandsWilke, Martina论文数: 0 引用数: 0 h-index: 0机构: Erasmus MC, Clin Genet, Rotterdam, Netherlands Erasmus MC, Clin Genet, Rotterdam, NetherlandsJoosten, Marieke论文数: 0 引用数: 0 h-index: 0机构: Erasmus MC, Clin Genet, Rotterdam, Netherlands Erasmus MC, Clin Genet, Rotterdam, Netherlandsvan den Born, Myrthe论文数: 0 引用数: 0 h-index: 0机构: Erasmus MC, Clin Genet, Rotterdam, Netherlands Erasmus MC, Clin Genet, Rotterdam, NetherlandsGaljaard, Robert-Jan论文数: 0 引用数: 0 h-index: 0机构: Erasmus MC, Clin Genet, Rotterdam, Netherlands Erasmus MC, Clin Genet, Rotterdam, NetherlandsWeerts, Marjolein论文数: 0 引用数: 0 h-index: 0机构: Erasmus MC, Clin Genet, Rotterdam, Netherlands Erasmus MC, Clin Genet, Rotterdam, Netherlandsvan Slegtenhorst, Marjon论文数: 0 引用数: 0 h-index: 0机构: Erasmus MC, Clin Genet, Rotterdam, Netherlands Erasmus MC, Clin Genet, Rotterdam, NetherlandsSleutels, Frank论文数: 0 引用数: 0 h-index: 0机构: Erasmus MC, Clin Genet, Rotterdam, Netherlands Erasmus MC, Clin Genet, Rotterdam, NetherlandsGaljaard, Sander论文数: 0 引用数: 0 h-index: 0机构: Erasmus MC, Obstet & Gynecol, Rotterdam, Netherlands Erasmus MC, Clin Genet, Rotterdam, NetherlandsKnapen, Maarten论文数: 0 引用数: 0 h-index: 0机构: Erasmus MC, Obstet & Gynecol, Rotterdam, Netherlands Erasmus MC, Clin Genet, Rotterdam, NetherlandsGo, Attie论文数: 0 引用数: 0 h-index: 0机构: Erasmus MC, Obstet & Gynecol, Rotterdam, Netherlands Erasmus MC, Clin Genet, Rotterdam, NetherlandsHoefsloot, Lies论文数: 0 引用数: 0 h-index: 0机构: Erasmus MC, Clin Genet, Rotterdam, Netherlands Erasmus MC, Clin Genet, Rotterdam, NetherlandsSrebniak, Malgorzata论文数: 0 引用数: 0 h-index: 0机构: Erasmus MC, Clin Genet, Rotterdam, Netherlands Erasmus MC, Clin Genet, Rotterdam, NetherlandsBruggenwirth, Hennie论文数: 0 引用数: 0 h-index: 0机构: Erasmus MC, Clin Genet, Rotterdam, Netherlands Erasmus MC, Clin Genet, Rotterdam, Netherlands
- [4] Prenatal exome sequencing in fetuses with callosal anomalies[J]. PRENATAL DIAGNOSIS, 2022, 42 (06) : 744 - 752Lei, Ting-ying论文数: 0 引用数: 0 h-index: 0机构: Guangzhou Med Univ, Prenatal Diagnost Ctr, Guangzhou Women & Childrens Med Ctr, 9 Jinsui Rd, Guangzhou, Guangdong, Peoples R China Guangzhou Med Univ, Prenatal Diagnost Ctr, Guangzhou Women & Childrens Med Ctr, 9 Jinsui Rd, Guangzhou, Guangdong, Peoples R ChinaShe, Qin论文数: 0 引用数: 0 h-index: 0机构: Guangzhou Med Univ, Prenatal Diagnost Ctr, Guangzhou Women & Childrens Med Ctr, 9 Jinsui Rd, Guangzhou, Guangdong, Peoples R China Guangzhou Med Univ, Affiliated Hosp 6, Prenatal Diagnost Ctr, Guangzhou, Peoples R China Guangzhou Med Univ, Prenatal Diagnost Ctr, Guangzhou Women & Childrens Med Ctr, 9 Jinsui Rd, Guangzhou, Guangdong, Peoples R ChinaFu, Fang论文数: 0 引用数: 0 h-index: 0机构: Guangzhou Med Univ, Eugen & Perinatal Inst, Guangzhou Women & Childrens Med Ctr, Guangzhou, Peoples R China Guangzhou Med Univ, Prenatal Diagnost Ctr, Guangzhou Women & Childrens Med Ctr, 9 Jinsui Rd, Guangzhou, Guangdong, Peoples R ChinaZhen, Li论文数: 0 引用数: 0 h-index: 0机构: Guangzhou Med Univ, Prenatal Diagnost Ctr, Guangzhou Women & Childrens Med Ctr, 9 Jinsui Rd, Guangzhou, Guangdong, Peoples R China Guangzhou Med Univ, Prenatal Diagnost Ctr, Guangzhou Women & Childrens Med Ctr, 9 Jinsui Rd, Guangzhou, Guangdong, Peoples R ChinaLi, Ru论文数: 0 引用数: 0 h-index: 0机构: Guangzhou Med Univ, Eugen & Perinatal Inst, Guangzhou Women & Childrens Med Ctr, Guangzhou, Peoples R China Guangzhou Med Univ, Prenatal Diagnost Ctr, Guangzhou Women & Childrens Med Ctr, 9 Jinsui Rd, Guangzhou, Guangdong, Peoples R ChinaYu, Qiu-xia论文数: 0 引用数: 0 h-index: 0机构: Guangzhou Med Univ, Eugen & Perinatal Inst, Guangzhou Women & Childrens Med Ctr, Guangzhou, Peoples R China Guangzhou Med Univ, Prenatal Diagnost Ctr, Guangzhou Women & Childrens Med Ctr, 9 Jinsui Rd, Guangzhou, Guangdong, Peoples R ChinaWang, Dan论文数: 0 引用数: 0 h-index: 0机构: Guangzhou Med Univ, Eugen & Perinatal Inst, Guangzhou Women & Childrens Med Ctr, Guangzhou, Peoples R China Guangzhou Med Univ, Prenatal Diagnost Ctr, Guangzhou Women & Childrens Med Ctr, 9 Jinsui Rd, Guangzhou, Guangdong, Peoples R ChinaLi, Ying-si论文数: 0 引用数: 0 h-index: 0机构: Guangzhou Med Univ, Eugen & Perinatal Inst, Guangzhou Women & Childrens Med Ctr, Guangzhou, Peoples R China Guangzhou Med Univ, Prenatal Diagnost Ctr, Guangzhou Women & Childrens Med Ctr, 9 Jinsui Rd, Guangzhou, Guangdong, Peoples R ChinaCheng, Ken论文数: 0 引用数: 0 h-index: 0机构: Guangzhou Med Univ, Eugen & Perinatal Inst, Guangzhou Women & Childrens Med Ctr, Guangzhou, Peoples R China Guangzhou Med Univ, Prenatal Diagnost Ctr, Guangzhou Women & Childrens Med Ctr, 9 Jinsui Rd, Guangzhou, Guangdong, Peoples R ChinaZhou, Hang论文数: 0 引用数: 0 h-index: 0机构: Guangzhou Med Univ, Eugen & Perinatal Inst, Guangzhou Women & Childrens Med Ctr, Guangzhou, Peoples R China Guangzhou Med Univ, Prenatal Diagnost Ctr, Guangzhou Women & Childrens Med Ctr, 9 Jinsui Rd, Guangzhou, Guangdong, Peoples R ChinaYang, Xin论文数: 0 引用数: 0 h-index: 0机构: Guangzhou Med Univ, Prenatal Diagnost Ctr, Guangzhou Women & Childrens Med Ctr, 9 Jinsui Rd, Guangzhou, Guangdong, Peoples R China Guangzhou Med Univ, Prenatal Diagnost Ctr, Guangzhou Women & Childrens Med Ctr, 9 Jinsui Rd, Guangzhou, Guangdong, Peoples R ChinaPan, Min论文数: 0 引用数: 0 h-index: 0机构: Guangzhou Med Univ, Prenatal Diagnost Ctr, Guangzhou Women & Childrens Med Ctr, 9 Jinsui Rd, Guangzhou, Guangdong, Peoples R China Guangzhou Med Univ, Prenatal Diagnost Ctr, Guangzhou Women & Childrens Med Ctr, 9 Jinsui Rd, Guangzhou, Guangdong, Peoples R ChinaLi, Dong-zhi论文数: 0 引用数: 0 h-index: 0机构: Guangzhou Med Univ, Prenatal Diagnost Ctr, Guangzhou Women & Childrens Med Ctr, 9 Jinsui Rd, Guangzhou, Guangdong, Peoples R China Guangzhou Med Univ, Prenatal Diagnost Ctr, Guangzhou Women & Childrens Med Ctr, 9 Jinsui Rd, Guangzhou, Guangdong, Peoples R ChinaLiao, Can论文数: 0 引用数: 0 h-index: 0机构: Guangzhou Med Univ, Prenatal Diagnost Ctr, Guangzhou Women & Childrens Med Ctr, 9 Jinsui Rd, Guangzhou, Guangdong, Peoples R China Guangzhou Med Univ, Prenatal Diagnost Ctr, Guangzhou Women & Childrens Med Ctr, 9 Jinsui Rd, Guangzhou, Guangdong, Peoples R China
- [5] Prenatal diagnosis by trio exome sequencing in fetuses with ultrasound anomalies: A powerful diagnostic tool[J]. FRONTIERS IN GENETICS, 2023, 14Tran Mau-Them, Frederic论文数: 0 引用数: 0 h-index: 0机构: CHU Dijon Bourgogne, Unite Fonctionnelle Innovat Diag Genom Maladies, Dijon, France INSERM, UMR1231 GAD, Dijon, France CHU Dijon Bourgogne, Unite Fonctionnelle Innovat Diag Genom Maladies, Dijon, FranceDelanne, Julian论文数: 0 引用数: 0 h-index: 0机构: CHU Dijon Bourgogne, Inst GIMI, Ctr Reference Malad Rares Anomalies Dev & Syndrom, Ctr Genet, Dijon, France CHU Dijon Bourgogne, FHU TRANSLAD, Dijon, France CHU Dijon Bourgogne, Unite Fonctionnelle Innovat Diag Genom Maladies, Dijon, FranceDenomme-Pichon, Anne-Sophie论文数: 0 引用数: 0 h-index: 0机构: CHU Dijon Bourgogne, Unite Fonctionnelle Innovat Diag Genom Maladies, Dijon, France INSERM, UMR1231 GAD, Dijon, France CHU Dijon Bourgogne, Unite Fonctionnelle Innovat Diag Genom Maladies, Dijon, FranceSafraou, Hana论文数: 0 引用数: 0 h-index: 0机构: CHU Dijon Bourgogne, Unite Fonctionnelle Innovat Diag Genom Maladies, Dijon, France INSERM, UMR1231 GAD, Dijon, France CHU Dijon Bourgogne, Unite Fonctionnelle Innovat Diag Genom Maladies, Dijon, FranceBruel, Ange-Line论文数: 0 引用数: 0 h-index: 0机构: CHU Dijon Bourgogne, Unite Fonctionnelle Innovat Diag Genom Maladies, Dijon, France INSERM, UMR1231 GAD, Dijon, France CHU Dijon Bourgogne, Unite Fonctionnelle Innovat Diag Genom Maladies, Dijon, FranceVitobello, Antonio论文数: 0 引用数: 0 h-index: 0机构: CHU Dijon Bourgogne, Unite Fonctionnelle Innovat Diag Genom Maladies, Dijon, France INSERM, UMR1231 GAD, Dijon, France CHU Dijon Bourgogne, Unite Fonctionnelle Innovat Diag Genom Maladies, Dijon, FranceGarde, Aurore论文数: 0 引用数: 0 h-index: 0机构: CHU Dijon Bourgogne, Inst GIMI, Ctr Reference Malad Rares Anomalies Dev & Syndrom, Ctr Genet, Dijon, France CHU Dijon Bourgogne, FHU TRANSLAD, Dijon, France CHU Dijon Bourgogne, Unite Fonctionnelle Innovat Diag Genom Maladies, Dijon, FranceNambot, Sophie论文数: 0 引用数: 0 h-index: 0机构: CHU Dijon Bourgogne, Inst GIMI, Ctr Reference Malad Rares Anomalies Dev & Syndrom, Ctr Genet, Dijon, France CHU Dijon Bourgogne, FHU TRANSLAD, Dijon, France CHU Dijon Bourgogne, Unite Fonctionnelle Innovat Diag Genom Maladies, Dijon, FranceBourgon, Nicolas论文数: 0 引用数: 0 h-index: 0机构: CHU Dijon Bourgogne, Inst GIMI, Ctr Reference Malad Rares Anomalies Dev & Syndrom, Ctr Genet, Dijon, France CHU Dijon Bourgogne, FHU TRANSLAD, Dijon, France CHU Dijon Bourgogne, Unite Fonctionnelle Innovat Diag Genom Maladies, Dijon, FranceRacine, Caroline论文数: 0 引用数: 0 h-index: 0机构: CHU Dijon Bourgogne, Inst GIMI, Ctr Reference Malad Rares Anomalies Dev & Syndrom, Ctr Genet, Dijon, France CHU Dijon Bourgogne, FHU TRANSLAD, Dijon, France CHU Dijon Bourgogne, Unite Fonctionnelle Innovat Diag Genom Maladies, Dijon, FranceSorlin, Arthur论文数: 0 引用数: 0 h-index: 0机构: INSERM, UMR1231 GAD, Dijon, France CHU Dijon Bourgogne, Inst GIMI, Ctr Reference Malad Rares Anomalies Dev & Syndrom, Ctr Genet, Dijon, France CHU Dijon Bourgogne, FHU TRANSLAD, Dijon, France CHU Dijon Bourgogne, Unite Fonctionnelle Innovat Diag Genom Maladies, Dijon, FranceMoutton, Sebastien论文数: 0 引用数: 0 h-index: 0机构: CHU Dijon Bourgogne, Inst GIMI, Ctr Reference Malad Rares Anomalies Dev & Syndrom, Ctr Genet, Dijon, France CHU Dijon Bourgogne, FHU TRANSLAD, Dijon, France CHU Dijon Bourgogne, Unite Fonctionnelle Innovat Diag Genom Maladies, Dijon, FranceMarle, Nathalie论文数: 0 引用数: 0 h-index: 0机构: CHU Dijon Bourgogne, Lab Genet Chromosom & Mol, Dijon, France CHU Dijon Bourgogne, Unite Fonctionnelle Innovat Diag Genom Maladies, Dijon, FranceRousseau, Thierry论文数: 0 引用数: 0 h-index: 0机构: Ctr Hosp Univ Dijon Bourgogne, Serv Gynecol Obstet Med Foetale & Sterilite Conju, Dijon, France CHU Dijon Bourgogne, Unite Fonctionnelle Innovat Diag Genom Maladies, Dijon, FranceSagot, Paul论文数: 0 引用数: 0 h-index: 0机构: Ctr Hosp Univ Dijon Bourgogne, Serv Gynecol Obstet Med Foetale & Sterilite Conju, Dijon, France CHU Dijon Bourgogne, Unite Fonctionnelle Innovat Diag Genom Maladies, Dijon, FranceSimon, Emmanuel论文数: 0 引用数: 0 h-index: 0机构: Ctr Hosp Univ Dijon Bourgogne, Serv Gynecol Obstet Med Foetale & Sterilite Conju, Dijon, France CHU Dijon Bourgogne, Unite Fonctionnelle Innovat Diag Genom Maladies, Dijon, FranceVincent-Delorme, Catherine论文数: 0 引用数: 0 h-index: 0机构: CHU Lille, Clin Genet Guy Fontaine, Ctr Reference Malad Rares Anomalies Dev & Syndrom, Lille, France CHU Dijon Bourgogne, Unite Fonctionnelle Innovat Diag Genom Maladies, Dijon, FranceBoute, Odile论文数: 0 引用数: 0 h-index: 0机构: CHU Lille, Clin Genet Guy Fontaine, Ctr Reference Malad Rares Anomalies Dev & Syndrom, Lille, France CHU Dijon Bourgogne, Unite Fonctionnelle Innovat Diag Genom Maladies, Dijon, FranceColson, Cindy论文数: 0 引用数: 0 h-index: 0机构: CHU Lille, Clin Genet Guy Fontaine, Ctr Reference Malad Rares Anomalies Dev & Syndrom, Lille, France CHU Dijon Bourgogne, Unite Fonctionnelle Innovat Diag Genom Maladies, Dijon, FrancePetit, Florence论文数: 0 引用数: 0 h-index: 0机构: CHU Lille, Clin Genet Guy Fontaine, Ctr Reference Malad Rares Anomalies Dev & Syndrom, Lille, France CHU Dijon Bourgogne, Unite Fonctionnelle Innovat Diag Genom Maladies, Dijon, FranceLegendre, Marine论文数: 0 引用数: 0 h-index: 0机构: CHU Bordeaux, Serv Genet Med, Bordeaux, France CHU Dijon Bourgogne, Unite Fonctionnelle Innovat Diag Genom Maladies, Dijon, FranceNaudion, Sophie论文数: 0 引用数: 0 h-index: 0机构: CHU Bordeaux, Serv Genet Med, Bordeaux, France CHU Dijon Bourgogne, Unite Fonctionnelle Innovat Diag Genom Maladies, Dijon, FranceRooryck, Caroline论文数: 0 引用数: 0 h-index: 0机构: CHU Bordeaux, Serv Genet Med, Bordeaux, France CHU Dijon Bourgogne, Unite Fonctionnelle Innovat Diag Genom Maladies, Dijon, FranceProuteau, Clement论文数: 0 引用数: 0 h-index: 0机构: Univ Hosp Angers, Biochem & Genet Dept, Angers, France CHU Dijon Bourgogne, Unite Fonctionnelle Innovat Diag Genom Maladies, Dijon, FranceColin, Estelle论文数: 0 引用数: 0 h-index: 0机构: Univ Hosp Angers, Biochem & Genet Dept, Angers, France CHU Dijon Bourgogne, Unite Fonctionnelle Innovat Diag Genom Maladies, Dijon, FranceGuichet, Agnes论文数: 0 引用数: 0 h-index: 0机构: Univ Hosp Angers, Biochem & Genet Dept, Angers, France CHU Dijon Bourgogne, Unite Fonctionnelle Innovat Diag Genom Maladies, Dijon, FranceZiegler, Alban论文数: 0 引用数: 0 h-index: 0机构: Univ Hosp Angers, Biochem & Genet Dept, Angers, France CHU Dijon Bourgogne, Unite Fonctionnelle Innovat Diag Genom Maladies, Dijon, FranceBonneau, Dominique论文数: 0 引用数: 0 h-index: 0机构: Univ Hosp Angers, Biochem & Genet Dept, Angers, France CHU Dijon Bourgogne, Unite Fonctionnelle Innovat Diag Genom Maladies, Dijon, FranceMorel, Godelieve论文数: 0 引用数: 0 h-index: 0机构: CHU Hop Sud, Ctr Reference Malad Rares CLAD Ouest, Serv Genet Clin, Rennes, France CHU Dijon Bourgogne, Unite Fonctionnelle Innovat Diag Genom Maladies, Dijon, FranceFradin, Melanie论文数: 0 引用数: 0 h-index: 0机构: CHU Hop Sud, Ctr Reference Malad Rares CLAD Ouest, Serv Genet Clin, Rennes, France CHU Dijon Bourgogne, Unite Fonctionnelle Innovat Diag Genom Maladies, Dijon, FranceLavillaureix, Alinoe论文数: 0 引用数: 0 h-index: 0机构: CHU Hop Sud, Ctr Reference Malad Rares CLAD Ouest, Serv Genet Clin, Rennes, France CHU Dijon Bourgogne, Unite Fonctionnelle Innovat Diag Genom Maladies, Dijon, FranceQuelin, Chloe论文数: 0 引用数: 0 h-index: 0机构: CHU Hop Sud, Ctr Reference Malad Rares CLAD Ouest, Serv Genet Clin, Rennes, France CHU Dijon Bourgogne, Unite Fonctionnelle Innovat Diag Genom Maladies, Dijon, FrancePasquier, Laurent论文数: 0 引用数: 0 h-index: 0机构: CHU Hop Sud, Ctr Reference Malad Rares CLAD Ouest, Serv Genet Clin, Rennes, France CHU Dijon Bourgogne, Unite Fonctionnelle Innovat Diag Genom Maladies, Dijon, FranceOdent, Sylvie论文数: 0 引用数: 0 h-index: 0机构: CHU Hop Sud, Ctr Reference Malad Rares CLAD Ouest, Serv Genet Clin, Rennes, France CHU Dijon Bourgogne, Unite Fonctionnelle Innovat Diag Genom Maladies, Dijon, FranceVera, Gabriella论文数: 0 引用数: 0 h-index: 0机构: Serv Genet Unite Genet Clin, Rouen, France CHU Dijon Bourgogne, Unite Fonctionnelle Innovat Diag Genom Maladies, Dijon, FranceGoldenberg, Alice论文数: 0 引用数: 0 h-index: 0机构: Serv Genet Unite Genet Clin, Rouen, France CHU Dijon Bourgogne, Unite Fonctionnelle Innovat Diag Genom Maladies, Dijon, FranceGuerrot, Anne-Marie论文数: 0 引用数: 0 h-index: 0机构: Serv Genet Unite Genet Clin, Rouen, France CHU Dijon Bourgogne, Unite Fonctionnelle Innovat Diag Genom Maladies, Dijon, FranceBrehin, Anne-Claire论文数: 0 引用数: 0 h-index: 0机构: Serv Genet Unite Genet Clin, Rouen, France CHU Dijon Bourgogne, Unite Fonctionnelle Innovat Diag Genom Maladies, Dijon, FrancePutoux, Audrey论文数: 0 引用数: 0 h-index: 0机构: Hop Femme Mere Enfant, Serv Genet, GH Est, Lyon, France CHU Dijon Bourgogne, Unite Fonctionnelle Innovat Diag Genom Maladies, Dijon, FranceAttia, Jocelyne论文数: 0 引用数: 0 h-index: 0机构: HCL, Serv Gynecol Obstet, Lyon, France CHU Dijon Bourgogne, Unite Fonctionnelle Innovat Diag Genom Maladies, Dijon, FranceAbel, Carine论文数: 0 引用数: 0 h-index: 0机构: CHU Lyon, HCL, GH Nord, Hop Croix Rousse,Serv Genet, Lyon, France CHU Lyon, Ctr Diagnost Antenatal, HCL, GH Nord,Hop Croix Rousse, Lyon, France CHU Dijon Bourgogne, Unite Fonctionnelle Innovat Diag Genom Maladies, Dijon, FranceBlanchet, Patricia论文数: 0 引用数: 0 h-index: 0机构: Univ Montpellier, CHU Montpellier, Equipe Malad Genet Enfant & Adulte, Dept Genet Med Malad Rares & Med Person, Montpellier, France CHU Dijon Bourgogne, Unite Fonctionnelle Innovat Diag Genom Maladies, Dijon, FranceWells, Constance F.论文数: 0 引用数: 0 h-index: 0机构: Univ Montpellier, CHU Montpellier, Equipe Malad Genet Enfant & Adulte, Dept Genet Med Malad Rares & Med Person, Montpellier, France CHU Dijon Bourgogne, Unite Fonctionnelle Innovat Diag Genom Maladies, Dijon, FranceDeiller, Caroline论文数: 0 引用数: 0 h-index: 0机构: Univ Montpellier, CHU Montpellier, Equipe Malad Genet Enfant & Adulte, Dept Genet Med Malad Rares & Med Person, Montpellier, France CHU Dijon Bourgogne, Unite Fonctionnelle Innovat Diag Genom Maladies, Dijon, FranceNizon, Mathilde论文数: 0 引用数: 0 h-index: 0机构: CHU Nantes, Serv Genet Med, Nantes, France Univ Nantes, CNRS, INSERM, Inst Thorax, Nantes, France CHU Dijon Bourgogne, Unite Fonctionnelle Innovat Diag Genom Maladies, Dijon, FranceMercier, Sandra论文数: 0 引用数: 0 h-index: 0机构: CHU Nantes, Serv Genet Med, Nantes, France Univ Nantes, CNRS, INSERM, Inst Thorax, Nantes, France CHU Dijon Bourgogne, Unite Fonctionnelle Innovat Diag Genom Maladies, Dijon, FranceVincent, Marie论文数: 0 引用数: 0 h-index: 0机构: CHU Nantes, Serv Genet Med, Nantes, France Univ Nantes, CNRS, INSERM, Inst Thorax, Nantes, France CHU Dijon Bourgogne, Unite Fonctionnelle Innovat Diag Genom Maladies, Dijon, FranceIsidor, Bertrand论文数: 0 引用数: 0 h-index: 0机构: CHU Nantes, Serv Genet Med, Nantes, France Univ Nantes, CNRS, INSERM, Inst Thorax, Nantes, France CHU Dijon Bourgogne, Unite Fonctionnelle Innovat Diag Genom Maladies, Dijon, FranceAmiel, Jeanne论文数: 0 引用数: 0 h-index: 0机构: Inst Malad Genet, Equipe Embryol & Genet Malformat Congenit, Inst Imagine, INSERM U1163, Paris, France Hop Necker Enfants Malad, Serv Genet Med & Clin, Paris, France CHU Dijon Bourgogne, Unite Fonctionnelle Innovat Diag Genom Maladies, Dijon, FranceDard, Rodolphe论文数: 0 引用数: 0 h-index: 0机构: Ctr Hosp Intercommunal Poissy St Germaine Laye, Unite Fonct Genet Med Cytogenet Genet Med & Biol, Poissy, France CHU Dijon Bourgogne, Unite Fonctionnelle Innovat Diag Genom Maladies, Dijon, France
- [6] Prenatal diagnosis of fetuses with ultrasound anomalies by whole-exome sequencing in Luoyang city, China[J]. FRONTIERS IN GENETICS, 2024, 14Wang, Yanan论文数: 0 引用数: 0 h-index: 0机构: Luoyang Maternal & Child Hlth Hosp, Dept Genet & Prenatal Diag, Luoyang, Peoples R China Luoyang Maternal & Child Hlth Hosp, Dept Genet & Prenatal Diag, Luoyang, Peoples R ChinaYin, Fan论文数: 0 引用数: 0 h-index: 0机构: Puluo Wuhan Med Biotechnol Co LTD, Wuhan, Peoples R China Luoyang Maternal & Child Hlth Hosp, Dept Genet & Prenatal Diag, Luoyang, Peoples R ChinaChai, Yuqiong论文数: 0 引用数: 0 h-index: 0机构: Luoyang Maternal & Child Hlth Hosp, Dept Genet & Prenatal Diag, Luoyang, Peoples R China Luoyang Maternal & Child Hlth Hosp, Dept Genet & Prenatal Diag, Luoyang, Peoples R ChinaJin, Jiapei论文数: 0 引用数: 0 h-index: 0机构: Luoyang Maternal & Child Hlth Hosp, Dept Genet & Prenatal Diag, Luoyang, Peoples R China Luoyang Maternal & Child Hlth Hosp, Dept Genet & Prenatal Diag, Luoyang, Peoples R ChinaZhang, Pai论文数: 0 引用数: 0 h-index: 0机构: Luoyang Maternal & Child Hlth Hosp, Dept Genet & Prenatal Diag, Luoyang, Peoples R China Luoyang Maternal & Child Hlth Hosp, Dept Genet & Prenatal Diag, Luoyang, Peoples R ChinaTan, Qianqian论文数: 0 引用数: 0 h-index: 0机构: Puluo Wuhan Med Biotechnol Co LTD, Wuhan, Peoples R China Luoyang Maternal & Child Hlth Hosp, Dept Genet & Prenatal Diag, Luoyang, Peoples R ChinaChen, Zhigang论文数: 0 引用数: 0 h-index: 0机构: Puluo Wuhan Med Biotechnol Co LTD, Wuhan, Peoples R China Luoyang Maternal & Child Hlth Hosp, Dept Genet & Prenatal Diag, Luoyang, Peoples R China
- [7] Prenatal Exome Sequencing Analysis in Fetuses with Various Ultrasound Findings[J]. JOURNAL OF CLINICAL MEDICINE, 2024, 13 (01)Borrell, Antoni论文数: 0 引用数: 0 h-index: 0机构: Univ Barcelona, Hosp Clin Barcelona, Barcelona Ctr Maternal Fetal & Neonatal Med BCNata, Barcelona 08007, Spain Univ Barcelona, Hosp Clin Barcelona, Barcelona Ctr Maternal Fetal & Neonatal Med BCNata, Barcelona 08007, SpainOrdonez, Elena论文数: 0 引用数: 0 h-index: 0机构: Veritas Genet, C Zamora 46-48, Barcelona 08005, Spain Univ Barcelona, Hosp Clin Barcelona, Barcelona Ctr Maternal Fetal & Neonatal Med BCNata, Barcelona 08007, SpainPauta, Montse论文数: 0 引用数: 0 h-index: 0机构: Inst Invest Biomed August Pi i Sunyer IDIBAPS, Barcelona 08036, Spain Univ Barcelona, Hosp Clin Barcelona, Barcelona Ctr Maternal Fetal & Neonatal Med BCNata, Barcelona 08007, SpainOtano, Juan论文数: 0 引用数: 0 h-index: 0机构: Univ Barcelona, Hosp Clin Barcelona, Barcelona Ctr Maternal Fetal & Neonatal Med BCNata, Barcelona 08007, Spain Univ Barcelona, Hosp Clin Barcelona, Barcelona Ctr Maternal Fetal & Neonatal Med BCNata, Barcelona 08007, SpainPaz-y-Mino, Fernanda论文数: 0 引用数: 0 h-index: 0机构: Univ Barcelona, Hosp Clin Barcelona, Barcelona Ctr Maternal Fetal & Neonatal Med BCNata, Barcelona 08007, Spain Univ Barcelona, Hosp Clin Barcelona, Barcelona Ctr Maternal Fetal & Neonatal Med BCNata, Barcelona 08007, Spainde Almeida, Mafalda论文数: 0 引用数: 0 h-index: 0机构: Veritas Genet, C Zamora 46-48, Barcelona 08005, Spain Univ Barcelona, Hosp Clin Barcelona, Barcelona Ctr Maternal Fetal & Neonatal Med BCNata, Barcelona 08007, SpainLeon, Miriam论文数: 0 引用数: 0 h-index: 0机构: Veritas Genet, C Zamora 46-48, Barcelona 08005, Spain Univ Barcelona, Hosp Clin Barcelona, Barcelona Ctr Maternal Fetal & Neonatal Med BCNata, Barcelona 08007, SpainCirigliano, Vincenzo论文数: 0 引用数: 0 h-index: 0机构: Veritas Genet, C Zamora 46-48, Barcelona 08005, Spain Univ Barcelona, Hosp Clin Barcelona, Barcelona Ctr Maternal Fetal & Neonatal Med BCNata, Barcelona 08007, Spain
- [8] Prenatal exome sequencing analysis in fetuses with central nervous system anomalies[J]. ULTRASOUND IN OBSTETRICS & GYNECOLOGY, 2023, 62 (05) : 721 - 726Zhi, Y.论文数: 0 引用数: 0 h-index: 0机构: Zhengzhou Univ, Affiliated Hosp 3, Prenatal Diag Ctr, 7 Kangfu Front St, Zhengzhou 450052, Henan, Peoples R China Zhengzhou Univ, Affiliated Hosp 3, Prenatal Diag Ctr, 7 Kangfu Front St, Zhengzhou 450052, Henan, Peoples R ChinaLiu, L.论文数: 0 引用数: 0 h-index: 0机构: Zhengzhou Univ, Affiliated Hosp 3, Prenatal Diag Ctr, 7 Kangfu Front St, Zhengzhou 450052, Henan, Peoples R China Zhengzhou Univ, Affiliated Hosp 3, Prenatal Diag Ctr, 7 Kangfu Front St, Zhengzhou 450052, Henan, Peoples R ChinaWang, H.论文数: 0 引用数: 0 h-index: 0机构: Zhengzhou Univ, Affiliated Hosp 3, Prenatal Diag Ctr, 7 Kangfu Front St, Zhengzhou 450052, Henan, Peoples R China Zhengzhou Univ, Affiliated Hosp 3, Prenatal Diag Ctr, 7 Kangfu Front St, Zhengzhou 450052, Henan, Peoples R ChinaChen, X.论文数: 0 引用数: 0 h-index: 0机构: Zhengzhou Univ, Affiliated Hosp 3, Prenatal Diag Ctr, 7 Kangfu Front St, Zhengzhou 450052, Henan, Peoples R China Zhengzhou Univ, Affiliated Hosp 3, Prenatal Diag Ctr, 7 Kangfu Front St, Zhengzhou 450052, Henan, Peoples R ChinaLv, Y.论文数: 0 引用数: 0 h-index: 0机构: Zhengzhou Univ, Affiliated Hosp 3, Prenatal Diag Ctr, 7 Kangfu Front St, Zhengzhou 450052, Henan, Peoples R China Zhengzhou Univ, Affiliated Hosp 3, Prenatal Diag Ctr, 7 Kangfu Front St, Zhengzhou 450052, Henan, Peoples R ChinaCui, X.论文数: 0 引用数: 0 h-index: 0机构: Zhengzhou Univ, Affiliated Hosp 3, Prenatal Diag Ctr, 7 Kangfu Front St, Zhengzhou 450052, Henan, Peoples R China Zhengzhou Univ, Affiliated Hosp 3, Prenatal Diag Ctr, 7 Kangfu Front St, Zhengzhou 450052, Henan, Peoples R ChinaChang, H.论文数: 0 引用数: 0 h-index: 0机构: Zhengzhou Univ, Affiliated Hosp 3, Sci Res Off, Zhengzhou, Henan, Peoples R China Zhengzhou Univ, Affiliated Hosp 3, Prenatal Diag Ctr, 7 Kangfu Front St, Zhengzhou 450052, Henan, Peoples R ChinaWang, Y.论文数: 0 引用数: 0 h-index: 0机构: Zhengzhou Univ, Affiliated Hosp 3, Clin Lab, Zhengzhou, Henan, Peoples R China Zhengzhou Univ, Affiliated Hosp 3, Prenatal Diag Ctr, 7 Kangfu Front St, Zhengzhou 450052, Henan, Peoples R ChinaCui, S.论文数: 0 引用数: 0 h-index: 0机构: Zhengzhou Univ, Affiliated Hosp 3, Prenatal Diag Ctr, 7 Kangfu Front St, Zhengzhou 450052, Henan, Peoples R China Zhengzhou Univ, Affiliated Hosp 3, Prenatal Diag Ctr, 7 Kangfu Front St, Zhengzhou 450052, Henan, Peoples R China
- [9] Prenatal diagnostic exome sequencing analysis in 207 fetuses with congenital CNS anomalies[J]. EUROPEAN JOURNAL OF HUMAN GENETICS, 2024, 32 : 502 - 502Kalanithy, Jeshurun Chiaran论文数: 0 引用数: 0 h-index: 0机构: Univ Bonn, Inst Neuroanat, Fac Med, Bonn, Germany Univ Bonn, Inst Human Genet, Fac Med, Bonn, Germany Univ Bonn, Inst Neuroanat, Fac Med, Bonn, GermanyThiele, Holger论文数: 0 引用数: 0 h-index: 0机构: Univ Cologne, Cologne Ctr Genom CCG, Cologne, Germany Univ Bonn, Inst Neuroanat, Fac Med, Bonn, GermanyWaffenschmidt, Lea论文数: 0 引用数: 0 h-index: 0机构: Friedrich Alexander Univ Erlangen Nurnberg, Dept Pediat & Adolescent Med, Erlangen, Germany Univ Bonn, Inst Neuroanat, Fac Med, Bonn, GermanyStegmann, Jil D.论文数: 0 引用数: 0 h-index: 0机构: Univ Bonn, Inst Human Genet, Fac Med, Bonn, Germany Univ Bonn, Inst Anat & Cell Biol, Fac Med, Bonn, Germany Univ Bonn, Inst Neuroanat, Fac Med, Bonn, GermanySchneider, Sophia论文数: 0 引用数: 0 h-index: 0机构: Univ Bonn, Inst Human Genet, Fac Med, Bonn, Germany Univ Bonn, Inst Neuroanat, Fac Med, Bonn, GermanyReutter, Heiko论文数: 0 引用数: 0 h-index: 0机构: Univ Bonn, Inst Human Genet, Fac Med, Bonn, Germany Friedrich Alexander Univ Erlangen Nurnberg, Inst Human Genet, Erlangen, Germany Friedrich Alexander Univ Erlangen Nurnberg, Div Neonatol & Pediat Intens Care, Dept Pediat & Adolescent Med, Erlangen, Germany Univ Bonn, Inst Neuroanat, Fac Med, Bonn, GermanyMerz, Waltraut论文数: 0 引用数: 0 h-index: 0机构: Univ Hosp Bonn, Dept Obstet & Prenatal Med, Bonn, Germany Univ Bonn, Inst Neuroanat, Fac Med, Bonn, GermanyDworschak, Gabriel论文数: 0 引用数: 0 h-index: 0机构: Univ Hosp Bonn, Dept Neuropediat, Bonn, Germany Univ Bonn, Inst Neuroanat, Fac Med, Bonn, Germany
- [10] Whole-exome sequencing in deceased fetuses with ultrasound anomalies: a retrospective analysis[J]. BMC MEDICAL GENOMICS, 2023, 16 (01)Huang, Wei论文数: 0 引用数: 0 h-index: 0机构: Zhengzhou Univ, Affiliated Hosp 1, Genet & Prenatal Diag Ctr, Dept Obstet & Gynecol, Zhengzhou 450052, Peoples R China Zhengzhou Univ, Affiliated Hosp 1, Genet & Prenatal Diag Ctr, Dept Obstet & Gynecol, Zhengzhou 450052, Peoples R ChinaZhu, Xiaofan论文数: 0 引用数: 0 h-index: 0机构: Zhengzhou Univ, Affiliated Hosp 1, Genet & Prenatal Diag Ctr, Dept Obstet & Gynecol, Zhengzhou 450052, Peoples R China Zhengzhou Univ, Affiliated Hosp 1, Genet & Prenatal Diag Ctr, Dept Obstet & Gynecol, Zhengzhou 450052, Peoples R ChinaSun, Gege论文数: 0 引用数: 0 h-index: 0机构: Zhengzhou Univ, Affiliated Hosp 1, Genet & Prenatal Diag Ctr, Dept Obstet & Gynecol, Zhengzhou 450052, Peoples R China Zhengzhou Univ, Affiliated Hosp 1, Genet & Prenatal Diag Ctr, Dept Obstet & Gynecol, Zhengzhou 450052, Peoples R ChinaGao, Zhi论文数: 0 引用数: 0 h-index: 0机构: Zhengzhou Univ, Affiliated Hosp 1, Genet & Prenatal Diag Ctr, Dept Obstet & Gynecol, Zhengzhou 450052, Peoples R China Zhengzhou Univ, Affiliated Hosp 1, Genet & Prenatal Diag Ctr, Dept Obstet & Gynecol, Zhengzhou 450052, Peoples R China论文数: 引用数: h-index:机构: