共 50 条
- [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] Use of prenatal exome sequencing in fetuses with ultrasound anomalies[J]. EUROPEAN JOURNAL OF HUMAN GENETICS, 2019, 27 : 11 - 12Segura-Puimedon, M.论文数: 0 引用数: 0 h-index: 0机构: qGenomics, Quantitat Genom Med Labs, Esplugas de Llobregat, Spain qGenomics, Quantitat Genom Med Labs, Esplugas de Llobregat, SpainRodriguez-Santiago, B.论文数: 0 引用数: 0 h-index: 0机构: qGenomics, Quantitat Genom Med Labs, Esplugas de Llobregat, Spain qGenomics, Quantitat Genom Med Labs, Esplugas de Llobregat, SpainVallmajo, A.论文数: 0 引用数: 0 h-index: 0机构: qGenomics, Quantitat Genom Med Labs, Esplugas de Llobregat, Spain qGenomics, Quantitat Genom Med Labs, Esplugas de Llobregat, SpainCodina-Sola, M.论文数: 0 引用数: 0 h-index: 0机构: qGenomics, Quantitat Genom Med Labs, Esplugas de Llobregat, Spain qGenomics, Quantitat Genom Med Labs, Esplugas de Llobregat, SpainCampos, B.论文数: 0 引用数: 0 h-index: 0机构: qGenomics, Quantitat Genom Med Labs, Esplugas de Llobregat, Spain qGenomics, Quantitat Genom Med Labs, Esplugas de Llobregat, SpainDatta, D.论文数: 0 引用数: 0 h-index: 0机构: qGenomics, Quantitat Genom Med Labs, Esplugas de Llobregat, Spain qGenomics, Quantitat Genom Med Labs, Esplugas de Llobregat, SpainBanchs, I.论文数: 0 引用数: 0 h-index: 0机构: qGenomics, Quantitat Genom Med Labs, Esplugas de Llobregat, Spain qGenomics, Quantitat Genom Med Labs, Esplugas de Llobregat, SpainMattlin, H.论文数: 0 引用数: 0 h-index: 0机构: qGenomics, Quantitat Genom Med Labs, Esplugas de Llobregat, Spain qGenomics, Quantitat Genom Med Labs, Esplugas de Llobregat, SpainSarria, Y.论文数: 0 引用数: 0 h-index: 0机构: qGenomics, Quantitat Genom Med Labs, Esplugas de Llobregat, Spain qGenomics, Quantitat Genom Med Labs, Esplugas de Llobregat, SpainAbad, O.论文数: 0 引用数: 0 h-index: 0机构: qGenomics, Quantitat Genom Med Labs, Esplugas de Llobregat, Spain qGenomics, Quantitat Genom Med Labs, Esplugas de Llobregat, SpainRodriguez, J.论文数: 0 引用数: 0 h-index: 0机构: qGenomics, Quantitat Genom Med Labs, Esplugas de Llobregat, Spain qGenomics, Quantitat Genom Med Labs, Esplugas de Llobregat, SpainPerez-Jurado, L.论文数: 0 引用数: 0 h-index: 0机构: qGenomics, Quantitat Genom Med Labs, Esplugas de Llobregat, Spain qGenomics, Quantitat Genom Med Labs, Esplugas de Llobregat, SpainArmengol, L.论文数: 0 引用数: 0 h-index: 0机构: qGenomics, Quantitat Genom Med Labs, Esplugas de Llobregat, Spain qGenomics, Quantitat Genom Med Labs, Esplugas de Llobregat, Spain
- [4] 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
- [5] 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
- [6] 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
- [7] Molecular diagnostic yield of exome sequencing in a Chinese cohort of 512 fetuses with anomalies[J]. BMC PREGNANCY AND CHILDBIRTH, 2024, 24 (01)Jin, Pengzhen论文数: 0 引用数: 0 h-index: 0机构: Zhejiang Univ, Womens Hosp, Sch Med, Hangzhou, Peoples R China Zhejiang Univ, Womens Hosp, Sch Med, Hangzhou, Peoples R ChinaHong, Jiawei论文数: 0 引用数: 0 h-index: 0机构: Zhejiang Univ, Womens Hosp, Sch Med, Hangzhou, Peoples R China Zhejiang Univ, Womens Hosp, Sch Med, Hangzhou, Peoples R ChinaXu, Yuqing论文数: 0 引用数: 0 h-index: 0机构: Zhejiang Univ, Womens Hosp, Sch Med, Hangzhou, Peoples R China Zhejiang Univ, Womens Hosp, Sch Med, Hangzhou, Peoples R ChinaQian, Yeqing论文数: 0 引用数: 0 h-index: 0机构: Zhejiang Univ, Womens Hosp, Sch Med, Hangzhou, Peoples R China Zhejiang Univ, Minist Educ, Key Lab Reprod Genet, Hangzhou, Peoples R China Zhejiang Univ, Womens Hosp, Sch Med, Hangzhou, Peoples R ChinaHan, Shuning论文数: 0 引用数: 0 h-index: 0机构: Zhejiang Univ, Womens Hosp, Sch Med, Hangzhou, Peoples R China Zhejiang Univ, Womens Hosp, Sch Med, Hangzhou, Peoples R ChinaDong, Minyue论文数: 0 引用数: 0 h-index: 0机构: Zhejiang Univ, Womens Hosp, Sch Med, Hangzhou, Peoples R China Zhejiang Univ, Minist Educ, Key Lab Reprod Genet, Hangzhou, Peoples R China Zhejiang Univ, Womens Hosp, Sch Med, Hangzhou, Peoples R China
- [8] Whole Exome Sequencing in 53 fetuses with abnormal ultrasound: 37% of diagnostic yield[J]. EUROPEAN JOURNAL OF HUMAN GENETICS, 2020, 28 (SUPPL 1) : 181 - 181Trost, D.论文数: 0 引用数: 0 h-index: 0机构: Lab Cerba, St Ouen, France Lab Cerba, St Ouen, FranceBoughalem, A.论文数: 0 引用数: 0 h-index: 0机构: Lab Cerba, St Ouen, France Lab Cerba, St Ouen, FranceBlanchet, P.论文数: 0 引用数: 0 h-index: 0机构: Hop Arnaud Villeneuve, Montpellier, France Lab Cerba, St Ouen, FranceCenni, C.论文数: 0 引用数: 0 h-index: 0机构: Hop Arnaud Villeneuve, Montpellier, France Lab Cerba, St Ouen, FranceDard, R.论文数: 0 引用数: 0 h-index: 0机构: Hop Poissy, Poissy, France Lab Cerba, St Ouen, FranceBenachi, A.论文数: 0 引用数: 0 h-index: 0机构: Hop Antoine Beclere, Clamart, France Lab Cerba, St Ouen, FranceCiorna-Monferrato, V.论文数: 0 引用数: 0 h-index: 0机构: Hop Metz Thionville, Metz, France Lab Cerba, St Ouen, FranceTouraine, R.论文数: 0 引用数: 0 h-index: 0机构: Hop Nord St Etienne, St Etienne, France Lab Cerba, St Ouen, FranceKleinfinger, P.论文数: 0 引用数: 0 h-index: 0机构: Lab Cerba, St Ouen, France Lab Cerba, St Ouen, FranceLohmann, L.论文数: 0 引用数: 0 h-index: 0机构: Lab Cerba, St Ouen, France Lab Cerba, St Ouen, FranceLuscan, A.论文数: 0 引用数: 0 h-index: 0机构: Lab Cerba, St Ouen, France Lab Cerba, St Ouen, FranceValduga, M.论文数: 0 引用数: 0 h-index: 0机构: Lab Cerba, St Ouen, France Lab Cerba, St Ouen, FranceCosta, J.论文数: 0 引用数: 0 h-index: 0机构: Lab Cerba, St Ouen, France Lab Cerba, St Ouen, France
- [9] 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
- [10] Diagnostic yield of prenatal-exome sequencing in the genetic screening of fetuses with brain anomalies: a systematic review and meta-analysis[J]. ULTRASOUND IN OBSTETRICS & GYNECOLOGY, 2023, 62 : 129 - 129Moradi, B.论文数: 0 引用数: 0 h-index: 0机构: Univ Tehran Med Sci, Adv Diagnost & Intervent Radiol Res Ctr, Tehran, Iran Univ Tehran Med Sci, Adv Diagnost & Intervent Radiol Res Ctr, Tehran, IranAriaei, A.论文数: 0 引用数: 0 h-index: 0机构: Univ Tehran Med Sci, Adv Diagnost & Intervent Radiol Res Ctr, Tehran, Iran Univ Tehran Med Sci, Adv Diagnost & Intervent Radiol Res Ctr, Tehran, IranHeidari-Foroozan, M.论文数: 0 引用数: 0 h-index: 0机构: Univ Tehran Med Sci, Adv Diagnost & Intervent Radiol Res Ctr, Tehran, Iran Univ Tehran Med Sci, Adv Diagnost & Intervent Radiol Res Ctr, Tehran, IranBanihashemian, M.论文数: 0 引用数: 0 h-index: 0机构: Univ Tehran Med Sci, Adv Diagnost & Intervent Radiol Res Ctr, Tehran, Iran Univ Tehran Med Sci, Adv Diagnost & Intervent Radiol Res Ctr, Tehran, IranGhorani, H.论文数: 0 引用数: 0 h-index: 0机构: Univ Tehran Med Sci, Adv Diagnost & Intervent Radiol Res Ctr, Tehran, Iran Univ Tehran Med Sci, Adv Diagnost & Intervent Radiol Res Ctr, Tehran, Iran论文数: 引用数: h-index:机构:论文数: 引用数: h-index:机构:论文数: 引用数: h-index:机构: