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- [22] Copy number variant detection increases diagnostic yield of Mendeliome sequencingEUROPEAN JOURNAL OF HUMAN GENETICS, 2019, 27 : 505 - 505Pajusalu, S.论文数: 0 引用数: 0 h-index: 0机构: Tartu Univ Hosp, United Labs, Dept Clin Genet, Tartu, Estonia Univ Tartu, Inst Clin Med, Dept Clin Genet, Tartu, Estonia Tartu Univ Hosp, United Labs, Dept Clin Genet, Tartu, EstoniaRoomere, H.论文数: 0 引用数: 0 h-index: 0机构: Tartu Univ Hosp, United Labs, Dept Clin Genet, Tartu, Estonia Tartu Univ Hosp, United Labs, Dept Clin Genet, Tartu, EstoniaKahre, T.论文数: 0 引用数: 0 h-index: 0机构: Tartu Univ Hosp, United Labs, Dept Clin Genet, Tartu, Estonia Univ Tartu, Inst Clin Med, Dept Clin Genet, Tartu, Estonia Tartu Univ Hosp, United Labs, Dept Clin Genet, Tartu, EstoniaMurumets, U.论文数: 0 引用数: 0 h-index: 0机构: Tartu Univ Hosp, United Labs, Dept Clin Genet, Tartu, Estonia Tartu Univ Hosp, United Labs, Dept Clin Genet, Tartu, EstoniaPata, V.论文数: 0 引用数: 0 h-index: 0机构: Tartu Univ Hosp, United Labs, Dept Clin Genet, Tartu, Estonia Tartu Univ Hosp, United Labs, Dept Clin Genet, Tartu, Estonia论文数: 引用数: h-index:机构:
- [23] Copy Number Analysis of Whole Exome Sequencing DataAMERICAN JOURNAL OF CLINICAL PATHOLOGY, 2024, 162 : S158 - S159Madubata, Chinwe论文数: 0 引用数: 0 h-index: 0机构: Columbia Univ, Dept Pathol & Cell Biol, Irving Med Ctr, New York, NY USA Columbia Univ, Dept Pathol & Cell Biol, Irving Med Ctr, New York, NY USABi, Xin论文数: 0 引用数: 0 h-index: 0机构: Columbia Univ, Dept Pathol & Cell Biol, Irving Med Ctr, New York, NY USA Columbia Univ, Dept Pathol & Cell Biol, Irving Med Ctr, New York, NY USAPang, Jiuhong论文数: 0 引用数: 0 h-index: 0机构: Columbia Univ, Dept Pathol & Cell Biol, Irving Med Ctr, New York, NY USA Columbia Univ, Dept Pathol & Cell Biol, Irving Med Ctr, New York, NY USAGu, Yue论文数: 0 引用数: 0 h-index: 0机构: Columbia Univ, Dept Pathol & Cell Biol, Irving Med Ctr, New York, NY USA Columbia Univ, Dept Pathol & Cell Biol, Irving Med Ctr, New York, NY USAKoganti, Lahari论文数: 0 引用数: 0 h-index: 0机构: Columbia Univ, Dept Pathol & Cell Biol, Irving Med Ctr, New York, NY USA Columbia Univ, Dept Pathol & Cell Biol, Irving Med Ctr, New York, NY USALiao, Jun论文数: 0 引用数: 0 h-index: 0机构: Columbia Univ, Dept Pathol & Cell Biol, Irving Med Ctr, New York, NY USA Columbia Univ, Dept Pathol & Cell Biol, Irving Med Ctr, New York, NY USAHsiao, Susan论文数: 0 引用数: 0 h-index: 0机构: Columbia Univ, Dept Pathol & Cell Biol, Irving Med Ctr, New York, NY USA Columbia Univ, Dept Pathol & Cell Biol, Irving Med Ctr, New York, NY USAAggarwal, Vimla论文数: 0 引用数: 0 h-index: 0机构: Columbia Univ, Dept Pathol & Cell Biol, Irving Med Ctr, New York, NY USA Columbia Univ, Dept Pathol & Cell Biol, Irving Med Ctr, New York, NY USAMansukhani, Mahesh论文数: 0 引用数: 0 h-index: 0机构: Columbia Univ, Dept Pathol & Cell Biol, Irving Med Ctr, New York, NY USA Columbia Univ, Dept Pathol & Cell Biol, Irving Med Ctr, New York, NY USAJobanputra, Vaidehi论文数: 0 引用数: 0 h-index: 0机构: Columbia Univ, Dept Pathol & Cell Biol, Irving Med Ctr, New York, NY USA Columbia Univ, Dept Pathol & Cell Biol, Irving Med Ctr, New York, NY USA
- [24] Comparative evaluation of Exome-CNV calling with Chromosomal Microarray Analysis for the identification of large copy number variationsEUROPEAN JOURNAL OF HUMAN GENETICS, 2020, 28 (SUPPL 1) : 616 - 617Tzur, S.论文数: 0 引用数: 0 h-index: 0机构: Emedgene Technol, Tel Aviv, Israel Emedgene Technol, Tel Aviv, IsraelKahana, S.论文数: 0 引用数: 0 h-index: 0机构: Beilinson Med Ctr, Rabin Med Ctr, Recanati Genet Inst, Petah Tiqwa, Israel Emedgene Technol, Tel Aviv, IsraelAttali, R.论文数: 0 引用数: 0 h-index: 0机构: Emedgene Technol, Tel Aviv, Israel Emedgene Technol, Tel Aviv, IsraelZinger, T.论文数: 0 引用数: 0 h-index: 0机构: Emedgene Technol, Tel Aviv, Israel Emedgene Technol, Tel Aviv, IsraelTalmy, T.论文数: 0 引用数: 0 h-index: 0机构: Emedgene Technol, Tel Aviv, Israel Emedgene Technol, Tel Aviv, IsraelSmirin-Yosef, P.论文数: 0 引用数: 0 h-index: 0机构: Emedgene Technol, Tel Aviv, Israel Emedgene Technol, Tel Aviv, IsraelMatar, R.论文数: 0 引用数: 0 h-index: 0机构: Beilinson Med Ctr, Rabin Med Ctr, Recanati Genet Inst, Petah Tiqwa, Israel Emedgene Technol, Tel Aviv, IsraelBazak, L.论文数: 0 引用数: 0 h-index: 0机构: Beilinson Med Ctr, Rabin Med Ctr, Recanati Genet Inst, Petah Tiqwa, Israel Tel Aviv Univ, Sackler Fac Med, Tel Aviv, Israel Emedgene Technol, Tel Aviv, IsraelRuhrman-Shahar, N.论文数: 0 引用数: 0 h-index: 0机构: Beilinson Med Ctr, Rabin Med Ctr, Recanati Genet Inst, Petah Tiqwa, Israel Emedgene Technol, Tel Aviv, IsraelBasel-Salmon, L.论文数: 0 引用数: 0 h-index: 0机构: Beilinson Med Ctr, Rabin Med Ctr, Recanati Genet Inst, Petah Tiqwa, Israel Tel Aviv Univ, Sackler Fac Med, Tel Aviv, Israel Schneider Childrens Med Ctr Israel, Pediat Genet Clin, Petah Tiqwa, Israel Felsenstein Med Res Ctr, Petah Tiqwa, Israel Emedgene Technol, Tel Aviv, Israel
- [25] Exome sequencing as a first-tier test for copy number variant detection: retrospective evaluation and prospective screening in 2418 casesJOURNAL OF MEDICAL GENETICS, 2022, 59 (12) : 1234 - 1240Testard, Quentin论文数: 0 引用数: 0 h-index: 0机构: Eurofins Biomnis, Serv Genet, Lyon, France CHU Grenoble Alpes, Serv Genet & Procreat, Grenoble, France Univ Grenoble Alpes, Inst Adv Biosci, U1209, CNRS,UMR 5309,INSERM, Grenoble, France Eurofins Biomnis, Serv Genet, Lyon, FranceVanhoye, Xavier论文数: 0 引用数: 0 h-index: 0机构: Eurofins Biomnis, Serv Genet, Lyon, France Eurofins Biomnis, Serv Genet, Lyon, FranceYauy, Kevin论文数: 0 引用数: 0 h-index: 0机构: Univ Grenoble Alpes, Inst Adv Biosci, U1209, CNRS,UMR 5309,INSERM, Grenoble, France SeqOne Genom, Montpellier, France Eurofins Biomnis, Serv Genet, Lyon, FranceNaud, Marie-Emmanuelle论文数: 0 引用数: 0 h-index: 0机构: Eurofins Biomnis, Serv Genet, Lyon, France Eurofins Biomnis, Serv Genet, Lyon, FranceVieville, Gaelle论文数: 0 引用数: 0 h-index: 0机构: CHU Grenoble Alpes, Serv Genet & Procreat, Grenoble, France Eurofins Biomnis, Serv Genet, Lyon, FranceRousseau, Francis论文数: 0 引用数: 0 h-index: 0机构: Eurofins Biomnis, Serv Genet, Lyon, France Eurofins Biomnis, Serv Genet, Lyon, FranceDauriat, Benjamin论文数: 0 引用数: 0 h-index: 0机构: CHU Limoges, Serv Cytogenet Genet Med & Biol Reprod, Limoges, France Eurofins Biomnis, Serv Genet, Lyon, FranceMarquet, Valentine论文数: 0 引用数: 0 h-index: 0机构: CHU Limoges, Serv Cytogenet Genet Med & Biol Reprod, Limoges, France Eurofins Biomnis, Serv Genet, Lyon, FranceBourthoumieu, Sylvie论文数: 0 引用数: 0 h-index: 0机构: CHU Limoges, Serv Cytogenet Genet Med & Biol Reprod, Limoges, France Eurofins Biomnis, Serv Genet, Lyon, France论文数: 引用数: h-index:机构:Gatinois, Vincent论文数: 0 引用数: 0 h-index: 0机构: CHU Montpellier, Dept Genet Med Malad Rares & Med Personnalisee, Montpellier, France Eurofins Biomnis, Serv Genet, Lyon, FranceWells, Constance论文数: 0 引用数: 0 h-index: 0机构: CHU Montpellier, Dept Genet Med Malad Rares & Med Personnalisee, Montpellier, France Eurofins Biomnis, Serv Genet, Lyon, FranceWillems, Marjolaine论文数: 0 引用数: 0 h-index: 0机构: CHU Montpellier, Dept Genet Med Malad Rares & Med Personnalisee, Montpellier, France Eurofins Biomnis, Serv Genet, Lyon, FranceCoubes, Christine论文数: 0 引用数: 0 h-index: 0机构: CHU Montpellier, Dept Genet Med Malad Rares & Med Personnalisee, Montpellier, France Eurofins Biomnis, Serv Genet, Lyon, FrancePinson, Lucile论文数: 0 引用数: 0 h-index: 0机构: CHU Montpellier, Dept Genet Med Malad Rares & Med Personnalisee, Montpellier, France Eurofins Biomnis, Serv Genet, Lyon, FranceDard, Rodolphe论文数: 0 引用数: 0 h-index: 0机构: CHI Poissy St Germain En Laye, Dept Genet, St Germain En Laye, France Eurofins Biomnis, Serv Genet, Lyon, FranceTessier, Aude论文数: 0 引用数: 0 h-index: 0机构: CHI Poissy St Germain En Laye, Dept Genet, St Germain En Laye, France Eurofins Biomnis, Serv Genet, Lyon, FranceHerve, Berenice论文数: 0 引用数: 0 h-index: 0机构: CHI Poissy St Germain En Laye, Dept Genet, St Germain En Laye, France Eurofins Biomnis, Serv Genet, Lyon, FranceVialard, Francois论文数: 0 引用数: 0 h-index: 0机构: CHI Poissy St Germain En Laye, Dept Genet, St Germain En Laye, France Eurofins Biomnis, Serv Genet, Lyon, FranceHarzallah, Ines论文数: 0 引用数: 0 h-index: 0机构: CHU St Etienne, Serv Genet Clin Chromosom & Mol, St Etienne, France Eurofins Biomnis, Serv Genet, Lyon, FranceTouraine, Renaud论文数: 0 引用数: 0 h-index: 0机构: CHU St Etienne, Serv Genet Clin Chromosom & Mol, St Etienne, France Eurofins Biomnis, Serv Genet, Lyon, FranceCogne, Benjamin论文数: 0 引用数: 0 h-index: 0机构: CHU Nantes, Serv Genet Med, Nantes, France Eurofins Biomnis, Serv Genet, Lyon, FranceDeb, Wallid论文数: 0 引用数: 0 h-index: 0机构: CHU Nantes, Serv Genet Med, Nantes, France Eurofins Biomnis, Serv Genet, Lyon, FranceBesnard, Thomas论文数: 0 引用数: 0 h-index: 0机构: CHU Nantes, Serv Genet Med, Nantes, France Eurofins Biomnis, Serv Genet, Lyon, FrancePichon, Olivier论文数: 0 引用数: 0 h-index: 0机构: CHU Nantes, Serv Genet Med, Nantes, France Eurofins Biomnis, Serv Genet, Lyon, FranceLaudier, Beatrice论文数: 0 引用数: 0 h-index: 0机构: CHR Orleans, Lab Immunol & Neurogenet Expt & Mol INEM UMR7355, Orleans, France Eurofins Biomnis, Serv Genet, Lyon, France论文数: 引用数: h-index:机构:Doreille, Alice论文数: 0 引用数: 0 h-index: 0机构: Sorbonne Univ, Hop Tenon, AP HP, Urgences Nephrol & Transplantat Renale, Paris, France Eurofins Biomnis, Serv Genet, Lyon, FranceBusa, Tiffany论文数: 0 引用数: 0 h-index: 0机构: Hop Timone Enfant, AP HM, Dept Genet Med, Marseille, France Eurofins Biomnis, Serv Genet, Lyon, FranceMissirian, Chantal论文数: 0 引用数: 0 h-index: 0机构: Hop Timone Enfant, AP HM, Dept Genet Med, Marseille, France Eurofins Biomnis, Serv Genet, Lyon, FranceSatre, Veronique论文数: 0 引用数: 0 h-index: 0机构: CHU Grenoble Alpes, Serv Genet & Procreat, Grenoble, France Univ Grenoble Alpes, Inst Adv Biosci, U1209, CNRS,UMR 5309,INSERM, Grenoble, France Eurofins Biomnis, Serv Genet, Lyon, France论文数: 引用数: h-index:机构:Celse, Tristan论文数: 0 引用数: 0 h-index: 0机构: CHU Grenoble Alpes, Serv Genet & Procreat, Grenoble, France Eurofins Biomnis, Serv Genet, Lyon, FranceHarbuz, Radu论文数: 0 引用数: 0 h-index: 0机构: CHU Grenoble Alpes, Serv Genet & Procreat, Grenoble, France Eurofins Biomnis, Serv Genet, Lyon, FranceRaymond, Laure论文数: 0 引用数: 0 h-index: 0机构: Eurofins Biomnis, Serv Genet, Lyon, France Eurofins Biomnis, Serv Genet, Lyon, FranceTaly, Jean-Francois论文数: 0 引用数: 0 h-index: 0机构: Eurofins Biomnis, Serv Genet, Lyon, France Eurofins Biomnis, Serv Genet, Lyon, FranceThevenon, Julien论文数: 0 引用数: 0 h-index: 0机构: CHU Grenoble Alpes, Serv Genet & Procreat, Grenoble, France Univ Grenoble Alpes, Inst Adv Biosci, U1209, CNRS,UMR 5309,INSERM, Grenoble, France Eurofins Biomnis, Serv Genet, Lyon, France
- [26] Detection of copy number variants and genes by chromosomal microarray in an Emirati neurodevelopmental disorders cohortNEUROGENETICS, 2022, 23 (02) : 137 - 149Nassir, Nasna论文数: 0 引用数: 0 h-index: 0机构: Mohammed Bin Rashid Univ Med & Hlth Sci, Coll Med, Dubai, U Arab Emirates Mohammed Bin Rashid Univ Med & Hlth Sci, Coll Med, Dubai, U Arab EmiratesSati, Isra论文数: 0 引用数: 0 h-index: 0机构: Al Jalila Childrens Hosp, Mental Hlth Ctr Excellence, Dubai, U Arab Emirates Monash Univ Malaysia, Jeffrey Cheah Sch Med & Hlth Sci, Brain Res Inst, Subang Jaya, Malaysia Mohammed Bin Rashid Univ Med & Hlth Sci, Coll Med, Dubai, U Arab EmiratesAl Shaibani, Shaiban论文数: 0 引用数: 0 h-index: 0机构: Mohammed Bin Rashid Univ Med & Hlth Sci, Coll Med, Dubai, U Arab Emirates Mohammed Bin Rashid Univ Med & Hlth Sci, Coll Med, Dubai, U Arab EmiratesAhmed, Awab论文数: 0 引用数: 0 h-index: 0机构: Mohammed Bin Rashid Univ Med & Hlth Sci, Coll Med, Dubai, U Arab Emirates Mohammed Bin Rashid Univ Med & Hlth Sci, Coll Med, Dubai, U Arab Emirates论文数: 引用数: h-index:机构:Akter, Hosneara论文数: 0 引用数: 0 h-index: 0机构: NeuroGen Childrens Healthcare, Genet & Genom Med Ctr, Dhaka, Bangladesh Mohammed Bin Rashid Univ Med & Hlth Sci, Coll Med, Dubai, U Arab EmiratesWoodbury-Smith, Marc论文数: 0 引用数: 0 h-index: 0机构: Newcastle Univ, Biosci Inst, Newcastle Upon Tyne, Tyne & Wear, England Mohammed Bin Rashid Univ Med & Hlth Sci, Coll Med, Dubai, U Arab EmiratesAbou Tayoun, Ahmad论文数: 0 引用数: 0 h-index: 0机构: Mohammed Bin Rashid Univ Med & Hlth Sci, Coll Med, Dubai, U Arab Emirates Al Jalila Childrens Hosp, Al Jalila Genom Ctr, Dubai, U Arab Emirates Mohammed Bin Rashid Univ Med & Hlth Sci, Coll Med, Dubai, U Arab EmiratesUddin, Mohammed论文数: 0 引用数: 0 h-index: 0机构: Mohammed Bin Rashid Univ Med & Hlth Sci, Coll Med, Dubai, U Arab Emirates GenomeArc Inc, Cellular Intelligence Ci Lab, Toronto, ON, Canada Mohammed Bin Rashid Univ Med & Hlth Sci, Coll Med, Dubai, U Arab EmiratesAlbanna, Ammar论文数: 0 引用数: 0 h-index: 0机构: Mohammed Bin Rashid Univ Med & Hlth Sci, Coll Med, Dubai, U Arab Emirates Al Jalila Childrens Hosp, Mental Hlth Ctr Excellence, Dubai, U Arab Emirates Mohammed Bin Rashid Univ Med & Hlth Sci, Coll Med, Dubai, U Arab Emirates
- [27] Detection of clinically relevant exonic copy number changes in fetuses by chromosomal microarray analysisGENETICS IN MEDICINE, 2022, 24 (03) : S291 - S291Owen, Nichole论文数: 0 引用数: 0 h-index: 0机构: Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USA Baylor Genet, Houston, TX USA Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USAOkur, Volkan论文数: 0 引用数: 0 h-index: 0机构: Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USA Baylor Genet, Houston, TX USA Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USAAnderson, Stephanie论文数: 0 引用数: 0 h-index: 0机构: Baylor Genet, Houston, TX USA Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USASmith, Janice论文数: 0 引用数: 0 h-index: 0机构: Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USA Baylor Genet, Houston, TX USA Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USABacino, Carlos论文数: 0 引用数: 0 h-index: 0机构: Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USA Baylor Genet, Houston, TX USA Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USAWard, Patricia论文数: 0 引用数: 0 h-index: 0机构: Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USA Baylor Genet, Houston, TX USA Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USACheung, Sau论文数: 0 引用数: 0 h-index: 0机构: Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USA Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USABreman, Amy论文数: 0 引用数: 0 h-index: 0机构: Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USA Baylor Genet, Houston, TX USA Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USAVan Den Veyver, Ignatia论文数: 0 引用数: 0 h-index: 0机构: Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USA Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USABi, Weimin论文数: 0 引用数: 0 h-index: 0机构: Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USA Baylor Genet, Houston, TX USA Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USA
- [28] Performance of Chromosomal Microarray Analysis for Detection of Copy Number Variations in Fetal Echogenic BowelRISK MANAGEMENT AND HEALTHCARE POLICY, 2021, 14 : 1431 - 1438Fan, Xiangqun论文数: 0 引用数: 0 h-index: 0机构: Fujian Med Univ, Affiliated Hosp, Fujian Matern & Child Hlth Hosp, Fujian Key Lab Prenatal Diag & Birth Defect, 18 Daoshan Rd, Fuzhou 350001, Fujian, Peoples R China Fujian Med Univ, Affiliated Hosp, Fujian Matern & Child Hlth Hosp, Fujian Key Lab Prenatal Diag & Birth Defect, 18 Daoshan Rd, Fuzhou 350001, Fujian, Peoples R ChinaHuang, Hailong论文数: 0 引用数: 0 h-index: 0机构: Fujian Med Univ, Affiliated Hosp, Fujian Matern & Child Hlth Hosp, Fujian Key Lab Prenatal Diag & Birth Defect, 18 Daoshan Rd, Fuzhou 350001, Fujian, Peoples R China Fujian Med Univ, Affiliated Hosp, Fujian Matern & Child Hlth Hosp, Fujian Key Lab Prenatal Diag & Birth Defect, 18 Daoshan Rd, Fuzhou 350001, Fujian, Peoples R ChinaLin, Xiyao论文数: 0 引用数: 0 h-index: 0机构: Fujian Med Univ, Sch Clin Med, Fuzhou 350122, Fujian, Peoples R China Fujian Med Univ, Affiliated Hosp, Fujian Matern & Child Hlth Hosp, Fujian Key Lab Prenatal Diag & Birth Defect, 18 Daoshan Rd, Fuzhou 350001, Fujian, Peoples R ChinaXuel, Huili论文数: 0 引用数: 0 h-index: 0机构: Fujian Med Univ, Affiliated Hosp, Fujian Matern & Child Hlth Hosp, Fujian Key Lab Prenatal Diag & Birth Defect, 18 Daoshan Rd, Fuzhou 350001, Fujian, Peoples R China Fujian Med Univ, Affiliated Hosp, Fujian Matern & Child Hlth Hosp, Fujian Key Lab Prenatal Diag & Birth Defect, 18 Daoshan Rd, Fuzhou 350001, Fujian, Peoples R ChinaCai, Meiying论文数: 0 引用数: 0 h-index: 0机构: Fujian Med Univ, Affiliated Hosp, Fujian Matern & Child Hlth Hosp, Fujian Key Lab Prenatal Diag & Birth Defect, 18 Daoshan Rd, Fuzhou 350001, Fujian, Peoples R China Fujian Med Univ, Affiliated Hosp, Fujian Matern & Child Hlth Hosp, Fujian Key Lab Prenatal Diag & Birth Defect, 18 Daoshan Rd, Fuzhou 350001, Fujian, Peoples R ChinaLin, Na论文数: 0 引用数: 0 h-index: 0机构: Fujian Med Univ, Affiliated Hosp, Fujian Matern & Child Hlth Hosp, Fujian Key Lab Prenatal Diag & Birth Defect, 18 Daoshan Rd, Fuzhou 350001, Fujian, Peoples R China Fujian Med Univ, Affiliated Hosp, Fujian Matern & Child Hlth Hosp, Fujian Key Lab Prenatal Diag & Birth Defect, 18 Daoshan Rd, Fuzhou 350001, Fujian, Peoples R ChinaXu, Liangpu论文数: 0 引用数: 0 h-index: 0机构: Fujian Med Univ, Affiliated Hosp, Fujian Matern & Child Hlth Hosp, Fujian Key Lab Prenatal Diag & Birth Defect, 18 Daoshan Rd, Fuzhou 350001, Fujian, Peoples R China Fujian Med Univ, Affiliated Hosp, Fujian Matern & Child Hlth Hosp, Fujian Key Lab Prenatal Diag & Birth Defect, 18 Daoshan Rd, Fuzhou 350001, Fujian, Peoples R China
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- [30] Detection of copy number variants and genes by chromosomal microarray in an Emirati neurodevelopmental disorders cohortneurogenetics, 2022, 23 : 137 - 149Nasna Nassir论文数: 0 引用数: 0 h-index: 0机构: Mohammed Bin Rashid University of Medicine and Health Sciences,College of MedicineIsra Sati论文数: 0 引用数: 0 h-index: 0机构: Mohammed Bin Rashid University of Medicine and Health Sciences,College of MedicineShaiban Al Shaibani论文数: 0 引用数: 0 h-index: 0机构: Mohammed Bin Rashid University of Medicine and Health Sciences,College of MedicineAwab Ahmed论文数: 0 引用数: 0 h-index: 0机构: Mohammed Bin Rashid University of Medicine and Health Sciences,College of MedicineOmar Almidani论文数: 0 引用数: 0 h-index: 0机构: Mohammed Bin Rashid University of Medicine and Health Sciences,College of MedicineHosneara Akter论文数: 0 引用数: 0 h-index: 0机构: Mohammed Bin Rashid University of Medicine and Health Sciences,College of MedicineMarc Woodbury-Smith论文数: 0 引用数: 0 h-index: 0机构: Mohammed Bin Rashid University of Medicine and Health Sciences,College of MedicineAhmad Abou Tayoun论文数: 0 引用数: 0 h-index: 0机构: Mohammed Bin Rashid University of Medicine and Health Sciences,College of MedicineMohammed Uddin论文数: 0 引用数: 0 h-index: 0机构: Mohammed Bin Rashid University of Medicine and Health Sciences,College of MedicineAmmar Albanna论文数: 0 引用数: 0 h-index: 0机构: Mohammed Bin Rashid University of Medicine and Health Sciences,College of Medicine