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- [1] WHOLE-EXOME-SEQUENCING IN CONGENITAL DISORDERS OF GLYCOSYLATIONJOURNAL OF INHERITED METABOLIC DISEASE, 2011, 34 : S180 - S180Timal, S.论文数: 0 引用数: 0 h-index: 0机构: Radboud Nijmegen Med Ctr, Nijmegen, Netherlands Radboud Nijmegen Med Ctr, Nijmegen, NetherlandsMorava, E.论文数: 0 引用数: 0 h-index: 0机构: Radboud Nijmegen Med Ctr, Nijmegen, Netherlands Radboud Nijmegen Med Ctr, Nijmegen, NetherlandsHoischen, A.论文数: 0 引用数: 0 h-index: 0机构: Radboud Nijmegen Med Ctr, Nijmegen, Netherlands Radboud Nijmegen Med Ctr, Nijmegen, NetherlandsVeltman, J.论文数: 0 引用数: 0 h-index: 0机构: Radboud Nijmegen Med Ctr, Nijmegen, Netherlands Radboud Nijmegen Med Ctr, Nijmegen, NetherlandsWevers, R. A.论文数: 0 引用数: 0 h-index: 0机构: Radboud Nijmegen Med Ctr, Nijmegen, Netherlands Radboud Nijmegen Med Ctr, Nijmegen, NetherlandsLefeber, D. J.论文数: 0 引用数: 0 h-index: 0机构: Radboud Nijmegen Med Ctr, Nijmegen, Netherlands Radboud Nijmegen Med Ctr, Nijmegen, Netherlands
- [2] Whole exome sequencing (WES) in prenatal diagnosis for carefully selected casesAMERICAN JOURNAL OF OBSTETRICS AND GYNECOLOGY, 2017, 216 (01) : S87 - S88Yadava, Stacy M.论文数: 0 引用数: 0 h-index: 0机构: Rutgers Robert Wood Johnson Med Sch, New Brunswick, NJ USA Rutgers Robert Wood Johnson Med Sch, New Brunswick, NJ USAAshkinadze, Elena论文数: 0 引用数: 0 h-index: 0机构: Rutgers Robert Wood Johnson Med Sch, New Brunswick, NJ USA Rutgers Robert Wood Johnson Med Sch, New Brunswick, NJ USA
- [3] Whole-exome sequencing for prenatal diagnosis of fetuses with congenital anomalies of the kidney and urinary tractNEPHROLOGY DIALYSIS TRANSPLANTATION, 2017, 32 (10) : 1665 - 1675Lei, Ting-ying论文数: 0 引用数: 0 h-index: 0机构: Guangzhou Med Univ, Guangzhou Women & Childrens Med Ctr, Prenatal Diagnost Ctr, Guangzhou, Guangdong, Peoples R China Guangzhou Med Univ, Guangzhou Women & Childrens Med Ctr, Prenatal Diagnost Ctr, Guangzhou, Guangdong, Peoples R ChinaFu, Fang论文数: 0 引用数: 0 h-index: 0机构: Guangzhou Med Univ, Guangzhou Women & Childrens Med Ctr, Eugen & Perinatal Inst, Guangzhou, Guangdong, Peoples R China Guangzhou Med Univ, Guangzhou Women & Childrens Med Ctr, Prenatal Diagnost Ctr, Guangzhou, Guangdong, Peoples R ChinaLi, Ru论文数: 0 引用数: 0 h-index: 0机构: Guangzhou Med Univ, Guangzhou Women & Childrens Med Ctr, Eugen & Perinatal Inst, Guangzhou, Guangdong, Peoples R China Guangzhou Med Univ, Guangzhou Women & Childrens Med Ctr, Prenatal Diagnost Ctr, Guangzhou, Guangdong, Peoples R ChinaWang, Dan论文数: 0 引用数: 0 h-index: 0机构: Guangzhou Med Univ, Guangzhou Women & Childrens Med Ctr, Eugen & Perinatal Inst, Guangzhou, Guangdong, Peoples R China Guangzhou Med Univ, Guangzhou Women & Childrens Med Ctr, Prenatal Diagnost Ctr, Guangzhou, Guangdong, Peoples R ChinaWang, Rong-yue论文数: 0 引用数: 0 h-index: 0机构: Guangzhou Med Univ, Guangzhou Women & Childrens Med Ctr, Prenatal Diagnost Ctr, Guangzhou, Guangdong, Peoples R China Guangzhou Med Univ, Guangzhou Women & Childrens Med Ctr, Prenatal Diagnost Ctr, Guangzhou, Guangdong, Peoples R ChinaJing, Xiang-yi论文数: 0 引用数: 0 h-index: 0机构: Guangzhou Med Univ, Guangzhou Women & Childrens Med Ctr, Eugen & Perinatal Inst, Guangzhou, Guangdong, Peoples R China Guangzhou Med Univ, Guangzhou Women & Childrens Med Ctr, Prenatal Diagnost Ctr, Guangzhou, Guangdong, Peoples R ChinaDeng, Qiong论文数: 0 引用数: 0 h-index: 0机构: Guangzhou Med Univ, Guangzhou Women & Childrens Med Ctr, Prenatal Diagnost Ctr, Guangzhou, Guangdong, Peoples R China Guangzhou Med Univ, Guangzhou Women & Childrens Med Ctr, Prenatal Diagnost Ctr, Guangzhou, Guangdong, Peoples R ChinaLi, Zhou-zhou论文数: 0 引用数: 0 h-index: 0机构: Guangzhou Med Univ, Guangzhou Women & Childrens Med Ctr, Prenatal Diagnost Ctr, Guangzhou, Guangdong, Peoples R China Guangzhou Med Univ, Guangzhou Women & Childrens Med Ctr, Prenatal Diagnost Ctr, Guangzhou, Guangdong, Peoples R ChinaLiu, Ze-qun论文数: 0 引用数: 0 h-index: 0机构: Guangzhou Med Univ, Guangzhou Women & Childrens Med Ctr, Eugen & Perinatal Inst, Guangzhou, Guangdong, Peoples R China Guangzhou Med Univ, Guangzhou Women & Childrens Med Ctr, Prenatal Diagnost Ctr, Guangzhou, Guangdong, Peoples R ChinaYang, Xin论文数: 0 引用数: 0 h-index: 0机构: Guangzhou Med Univ, Guangzhou Women & Childrens Med Ctr, Prenatal Diagnost Ctr, Guangzhou, Guangdong, Peoples R China Guangzhou Med Univ, Guangzhou Women & Childrens Med Ctr, Prenatal Diagnost Ctr, Guangzhou, Guangdong, Peoples R ChinaLi, Dong-zhi论文数: 0 引用数: 0 h-index: 0机构: Guangzhou Med Univ, Guangzhou Women & Childrens Med Ctr, Prenatal Diagnost Ctr, Guangzhou, Guangdong, Peoples R China Guangzhou Med Univ, Guangzhou Women & Childrens Med Ctr, Prenatal Diagnost Ctr, Guangzhou, Guangdong, Peoples R ChinaLiao, Can论文数: 0 引用数: 0 h-index: 0机构: Guangzhou Med Univ, Guangzhou Women & Childrens Med Ctr, Prenatal Diagnost Ctr, Guangzhou, Guangdong, Peoples R China Guangzhou Med Univ, Guangzhou Women & Childrens Med Ctr, Prenatal Diagnost Ctr, Guangzhou, Guangdong, Peoples R China
- [4] Clinical utility of exome sequencing in the prenatal diagnosis of congenital anomalies: A ReviewEUROPEAN JOURNAL OF OBSTETRICS & GYNECOLOGY AND REPRODUCTIVE BIOLOGY, 2018, 231 : 19 - 24Mone, Fionnuala论文数: 0 引用数: 0 h-index: 0机构: Birmingham Womens & Childrens NHS Fdn Trust, Dept Clin Genet, Mindelsohn Way, Birmingham B15 2TG, W Midlands, England Birmingham Womens & Childrens NHS Fdn Trust, West Midlands Fetal Med Ctr, Mindelsohn Way, Birmingham B15 2TG, W Midlands, England Birmingham Womens & Childrens NHS Fdn Trust, Dept Clin Genet, Mindelsohn Way, Birmingham B15 2TG, W Midlands, EnglandQuinlan-Jones, Elizabeth论文数: 0 引用数: 0 h-index: 0机构: Birmingham Womens & Childrens NHS Fdn Trust, Dept Clin Genet, Mindelsohn Way, Birmingham B15 2TG, W Midlands, England Birmingham Womens & Childrens NHS Fdn Trust, West Midlands Fetal Med Ctr, Mindelsohn Way, Birmingham B15 2TG, W Midlands, England Birmingham Womens & Childrens NHS Fdn Trust, Dept Clin Genet, Mindelsohn Way, Birmingham B15 2TG, W Midlands, EnglandKilby, Mark D.论文数: 0 引用数: 0 h-index: 0机构: Birmingham Womens & Childrens NHS Fdn Trust, West Midlands Fetal Med Ctr, Mindelsohn Way, Birmingham B15 2TG, W Midlands, England Univ Birmingham, Inst Metab & Syst Res, Ctr Womens & New Born Hlth, Birmingham, W Midlands, England Birmingham Womens & Childrens NHS Fdn Trust, Dept Clin Genet, Mindelsohn Way, Birmingham B15 2TG, W Midlands, England
- [5] Diagnosis of Williams Syndrome by Whole Exome Sequencing (WES)EUROPEAN JOURNAL OF HUMAN GENETICS, 2023, 31 : 202 - 202Tilemis, Faidon-Nikolaos论文数: 0 引用数: 0 h-index: 0机构: Natl & Kapodistrian Univ Athens, Med Sch, St Sophias Childrens Hosp, Lab Med Genet, Athens, Greece Natl & Kapodistrian Univ Athens, Res Univ Inst Study & Prevent Genet & Malignant D, St Sophias Childrens Hosp, Athens, Greece Natl & Kapodistrian Univ Athens, Med Sch, St Sophias Childrens Hosp, Lab Med Genet, Athens, GreeceVeltra, Danai论文数: 0 引用数: 0 h-index: 0机构: Natl & Kapodistrian Univ Athens, Med Sch, St Sophias Childrens Hosp, Lab Med Genet, Athens, Greece Natl & Kapodistrian Univ Athens, Med Sch, St Sophias Childrens Hosp, Lab Med Genet, Athens, GreeceMarinakis, Nikolaos论文数: 0 引用数: 0 h-index: 0机构: Natl & Kapodistrian Univ Athens, Med Sch, St Sophias Childrens Hosp, Lab Med Genet, Athens, Greece Natl & Kapodistrian Univ Athens, Med Sch, St Sophias Childrens Hosp, Lab Med Genet, Athens, GreeceSvingou, Maria论文数: 0 引用数: 0 h-index: 0机构: Natl & Kapodistrian Univ Athens, Med Sch, St Sophias Childrens Hosp, Lab Med Genet, Athens, Greece Natl & Kapodistrian Univ Athens, Med Sch, St Sophias Childrens Hosp, Lab Med Genet, Athens, GreeceKosma, Konstantina论文数: 0 引用数: 0 h-index: 0机构: Natl & Kapodistrian Univ Athens, Med Sch, St Sophias Childrens Hosp, Lab Med Genet, Athens, Greece Natl & Kapodistrian Univ Athens, Med Sch, St Sophias Childrens Hosp, Lab Med Genet, Athens, GreeceTraeger-Synodinos, Jan论文数: 0 引用数: 0 h-index: 0机构: Natl & Kapodistrian Univ Athens, Med Sch, St Sophias Childrens Hosp, Lab Med Genet, Athens, Greece Natl & Kapodistrian Univ Athens, Med Sch, St Sophias Childrens Hosp, Lab Med Genet, Athens, GreeceSofocleous, Christalena论文数: 0 引用数: 0 h-index: 0机构: Natl & Kapodistrian Univ Athens, Med Sch, St Sophias Childrens Hosp, Lab Med Genet, Athens, Greece Natl & Kapodistrian Univ Athens, Res Univ Inst Study & Prevent Genet & Malignant D, St Sophias Childrens Hosp, Athens, Greece Natl & Kapodistrian Univ Athens, Med Sch, St Sophias Childrens Hosp, Lab Med Genet, Athens, Greece
- [6] ARTHROGRYPOSIS MULTIPLEX CONGENITA TYPE 6: PRENATAL DIAGNOSIS THROUGH THE POWER OF WHOLE EXOME SEQUENCING (WES)MEDICINE, 2025, 104 (04)Conceicao, Ariana论文数: 0 引用数: 0 h-index: 0机构: SynlabHlth Genet Med, Unidade Genet Mol & Genom, Porto, Portugal SynlabHlth Genet Med, Unidade Genet Mol & Genom, Porto, PortugalSalgueiro, Natalia论文数: 0 引用数: 0 h-index: 0机构: SynlabHlth Genet Med, Unidade Genet Mol & Genom, Porto, Portugal SynlabHlth Genet Med, Unidade Genet Mol & Genom, Porto, PortugalCastro, Lisandra论文数: 0 引用数: 0 h-index: 0机构: SynlabHlth Genet Med, Unidade Genet Mol & Genom, Porto, Portugal SynlabHlth Genet Med, Unidade Genet Mol & Genom, Porto, PortugalAlves, Claudia论文数: 0 引用数: 0 h-index: 0机构: SynlabHlth Genet Med, Unidade Citogenet, Porto, Portugal SynlabHlth Genet Med, Unidade Genet Mol & Genom, Porto, PortugalDantas, Marcelo论文数: 0 引用数: 0 h-index: 0机构: SynlabHlth Genet Med, Unidade Genet Mol & Genom, Porto, Portugal SynlabHlth Genet Med, Unidade Genet Mol & Genom, Porto, PortugalMata, Joao论文数: 0 引用数: 0 h-index: 0机构: SynlabHlth Genet Med, Unidade Genet Mol & Genom, Porto, Portugal SynlabHlth Genet Med, Unidade Genet Mol & Genom, Porto, PortugalMendes, Celia论文数: 0 引用数: 0 h-index: 0机构: SynlabHlth Genet Med, Unidade Genet Mol & Genom, Porto, Portugal SynlabHlth Genet Med, Unidade Genet Mol & Genom, Porto, PortugalGarcia, Elsa论文数: 0 引用数: 0 h-index: 0机构: SynlabHlth Genet Med, Unidade Genet Mol & Genom, Porto, Portugal SynlabHlth Genet Med, Unidade Genet Mol & Genom, Porto, PortugalTrindade, Joana论文数: 0 引用数: 0 h-index: 0机构: SynlabHlth Genet Med, Unidade Citogenet, Porto, Portugal SynlabHlth Genet Med, Unidade Genet Mol & Genom, Porto, PortugalLadeira, Guilhermina论文数: 0 引用数: 0 h-index: 0机构: Hosp Cascais, Unidade Obstet, Lisbon, Portugal SynlabHlth Genet Med, Unidade Genet Mol & Genom, Porto, PortugalLima, Margarida R.论文数: 0 引用数: 0 h-index: 0机构: SynlabHlth Genet Med, Unidade Genet Mol & Genom, Porto, Portugal SynlabHlth Genet Med, Unidade Genet Mol & Genom, Porto, Portugal
- [7] Identifying the genetic causes for prenatally diagnosed structural congenital anomalies (SCAs) by whole-exome sequencing (WES)BMC Medical Genomics, 11Gordon K C Leung论文数: 0 引用数: 0 h-index: 0机构: The University of Hong Kong,Department of Paediatrics and Adolescent Medicine, LKS Faculty of MedicineChristopher C Y Mak论文数: 0 引用数: 0 h-index: 0机构: The University of Hong Kong,Department of Paediatrics and Adolescent Medicine, LKS Faculty of MedicineJasmine L F Fung论文数: 0 引用数: 0 h-index: 0机构: The University of Hong Kong,Department of Paediatrics and Adolescent Medicine, LKS Faculty of MedicineWilfred H S Wong论文数: 0 引用数: 0 h-index: 0机构: The University of Hong Kong,Department of Paediatrics and Adolescent Medicine, LKS Faculty of MedicineMandy H Y Tsang论文数: 0 引用数: 0 h-index: 0机构: The University of Hong Kong,Department of Paediatrics and Adolescent Medicine, LKS Faculty of MedicineMullin H C Yu论文数: 0 引用数: 0 h-index: 0机构: The University of Hong Kong,Department of Paediatrics and Adolescent Medicine, LKS Faculty of MedicineSteven L C Pei论文数: 0 引用数: 0 h-index: 0机构: The University of Hong Kong,Department of Paediatrics and Adolescent Medicine, LKS Faculty of MedicineK S Yeung论文数: 0 引用数: 0 h-index: 0机构: The University of Hong Kong,Department of Paediatrics and Adolescent Medicine, LKS Faculty of MedicineGary T K Mok论文数: 0 引用数: 0 h-index: 0机构: The University of Hong Kong,Department of Paediatrics and Adolescent Medicine, LKS Faculty of MedicineC P Lee论文数: 0 引用数: 0 h-index: 0机构: The University of Hong Kong,Department of Paediatrics and Adolescent Medicine, LKS Faculty of MedicineAmelia P W Hui论文数: 0 引用数: 0 h-index: 0机构: The University of Hong Kong,Department of Paediatrics and Adolescent Medicine, LKS Faculty of MedicineMary H Y Tang论文数: 0 引用数: 0 h-index: 0机构: The University of Hong Kong,Department of Paediatrics and Adolescent Medicine, LKS Faculty of MedicineKelvin Y K Chan论文数: 0 引用数: 0 h-index: 0机构: The University of Hong Kong,Department of Paediatrics and Adolescent Medicine, LKS Faculty of MedicineAnthony P Y Liu论文数: 0 引用数: 0 h-index: 0机构: The University of Hong Kong,Department of Paediatrics and Adolescent Medicine, LKS Faculty of MedicineWanling Yang论文数: 0 引用数: 0 h-index: 0机构: The University of Hong Kong,Department of Paediatrics and Adolescent Medicine, LKS Faculty of MedicineP C Sham论文数: 0 引用数: 0 h-index: 0机构: The University of Hong Kong,Department of Paediatrics and Adolescent Medicine, LKS Faculty of MedicineAnita S Y Kan论文数: 0 引用数: 0 h-index: 0机构: The University of Hong Kong,Department of Paediatrics and Adolescent Medicine, LKS Faculty of MedicineBrian H Y Chung论文数: 0 引用数: 0 h-index: 0机构: The University of Hong Kong,Department of Paediatrics and Adolescent Medicine, LKS Faculty of Medicine
- [8] Identifying the genetic causes for prenatally diagnosed structural congenital anomalies (SCAs) by whole-exome sequencing (WES)BMC MEDICAL GENOMICS, 2018, 11Leung, Gordon K. C.论文数: 0 引用数: 0 h-index: 0机构: Univ Hong Kong, LKS Fac Med, Dept Paediat & Adolescent Med, Room 103,1-F New Clin Bldg, Hong Kong, Hong Kong, Peoples R China Univ Hong Kong, LKS Fac Med, Dept Paediat & Adolescent Med, Room 103,1-F New Clin Bldg, Hong Kong, Hong Kong, Peoples R ChinaMak, Christopher C. Y.论文数: 0 引用数: 0 h-index: 0机构: Univ Hong Kong, LKS Fac Med, Dept Paediat & Adolescent Med, Room 103,1-F New Clin Bldg, Hong Kong, Hong Kong, Peoples R China Univ Hong Kong, LKS Fac Med, Dept Paediat & Adolescent Med, Room 103,1-F New Clin Bldg, Hong Kong, Hong Kong, Peoples R ChinaFung, Jasmine L. F.论文数: 0 引用数: 0 h-index: 0机构: Univ Hong Kong, LKS Fac Med, Dept Paediat & Adolescent Med, Room 103,1-F New Clin Bldg, Hong Kong, Hong Kong, Peoples R China Univ Hong Kong, LKS Fac Med, Dept Paediat & Adolescent Med, Room 103,1-F New Clin Bldg, Hong Kong, Hong Kong, Peoples R ChinaWong, Wilfred H. S.论文数: 0 引用数: 0 h-index: 0机构: Univ Hong Kong, LKS Fac Med, Dept Paediat & Adolescent Med, Room 103,1-F New Clin Bldg, Hong Kong, Hong Kong, Peoples R China Univ Hong Kong, LKS Fac Med, Dept Paediat & Adolescent Med, Room 103,1-F New Clin Bldg, Hong Kong, Hong Kong, Peoples R ChinaTsang, Mandy H. Y.论文数: 0 引用数: 0 h-index: 0机构: Univ Hong Kong, LKS Fac Med, Dept Paediat & Adolescent Med, Room 103,1-F New Clin Bldg, Hong Kong, Hong Kong, Peoples R China Univ Hong Kong, LKS Fac Med, Dept Paediat & Adolescent Med, Room 103,1-F New Clin Bldg, Hong Kong, Hong Kong, Peoples R ChinaYu, Mullin H. C.论文数: 0 引用数: 0 h-index: 0机构: Univ Hong Kong, LKS Fac Med, Dept Paediat & Adolescent Med, Room 103,1-F New Clin Bldg, Hong Kong, Hong Kong, Peoples R China Univ Hong Kong, LKS Fac Med, Dept Paediat & Adolescent Med, Room 103,1-F New Clin Bldg, Hong Kong, Hong Kong, Peoples R ChinaPei, Steven L. C.论文数: 0 引用数: 0 h-index: 0机构: Univ Hong Kong, LKS Fac Med, Dept Paediat & Adolescent Med, Room 103,1-F New Clin Bldg, Hong Kong, Hong Kong, Peoples R China Univ Hong Kong, LKS Fac Med, Dept Paediat & Adolescent Med, Room 103,1-F New Clin Bldg, Hong Kong, Hong Kong, Peoples R ChinaYeung, K. S.论文数: 0 引用数: 0 h-index: 0机构: Univ Hong Kong, LKS Fac Med, Dept Paediat & Adolescent Med, Room 103,1-F New Clin Bldg, Hong Kong, Hong Kong, Peoples R China Univ Hong Kong, LKS Fac Med, Dept Paediat & Adolescent Med, Room 103,1-F New Clin Bldg, Hong Kong, Hong Kong, Peoples R ChinaMok, Gary T. K.论文数: 0 引用数: 0 h-index: 0机构: Univ Hong Kong, LKS Fac Med, Dept Paediat & Adolescent Med, Room 103,1-F New Clin Bldg, Hong Kong, Hong Kong, Peoples R China Univ Hong Kong, LKS Fac Med, Dept Paediat & Adolescent Med, Room 103,1-F New Clin Bldg, Hong Kong, Hong Kong, Peoples R ChinaLee, C. P.论文数: 0 引用数: 0 h-index: 0机构: Univ Hong Kong, Queen Mary Hosp, Dept Obstet & Gynaecol, Hong Kong, Hong Kong, Peoples R China Univ Hong Kong, LKS Fac Med, Dept Paediat & Adolescent Med, Room 103,1-F New Clin Bldg, Hong Kong, Hong Kong, Peoples R ChinaHui, Amelia P. W.论文数: 0 引用数: 0 h-index: 0机构: Univ Hong Kong, Queen Mary Hosp, Dept Obstet & Gynaecol, Hong Kong, Hong Kong, Peoples R China Univ Hong Kong, LKS Fac Med, Dept Paediat & Adolescent Med, Room 103,1-F New Clin Bldg, Hong Kong, Hong Kong, Peoples R ChinaTang, Mary H. Y.论文数: 0 引用数: 0 h-index: 0机构: Univ Hong Kong, Queen Mary Hosp, Dept Obstet & Gynaecol, Hong Kong, Hong Kong, Peoples R China Tsan Yuk Hosp, Dept Obstet & Gynaecol, Prenatal Diagnost Lab, Hong Kong, Hong Kong, Peoples R China Univ Hong Kong, LKS Fac Med, Dept Paediat & Adolescent Med, Room 103,1-F New Clin Bldg, Hong Kong, Hong Kong, Peoples R ChinaChan, Kelvin Y. K.论文数: 0 引用数: 0 h-index: 0机构: Univ Hong Kong, Queen Mary Hosp, Dept Obstet & Gynaecol, Hong Kong, Hong Kong, Peoples R China Tsan Yuk Hosp, Dept Obstet & Gynaecol, Prenatal Diagnost Lab, Hong Kong, Hong Kong, Peoples R China Univ Hong Kong, LKS Fac Med, Dept Paediat & Adolescent Med, Room 103,1-F New Clin Bldg, Hong Kong, Hong Kong, Peoples R ChinaLiu, Anthony P. Y.论文数: 0 引用数: 0 h-index: 0机构: Univ Hong Kong, LKS Fac Med, Dept Paediat & Adolescent Med, Room 103,1-F New Clin Bldg, Hong Kong, Hong Kong, Peoples R China Univ Hong Kong, LKS Fac Med, Dept Paediat & Adolescent Med, Room 103,1-F New Clin Bldg, Hong Kong, Hong Kong, Peoples R ChinaYang, Wanling论文数: 0 引用数: 0 h-index: 0机构: Univ Hong Kong, LKS Fac Med, Dept Paediat & Adolescent Med, Room 103,1-F New Clin Bldg, Hong Kong, Hong Kong, Peoples R China Univ Hong Kong, LKS Fac Med, Dept Paediat & Adolescent Med, Room 103,1-F New Clin Bldg, Hong Kong, Hong Kong, Peoples R ChinaSham, P. C.论文数: 0 引用数: 0 h-index: 0机构: Univ Hong Kong, LKS Fac Med, Dept Psychiat, Hong Kong, Hong Kong, Peoples R China Univ Hong Kong, LKS Fac Med, Dept Paediat & Adolescent Med, Room 103,1-F New Clin Bldg, Hong Kong, Hong Kong, Peoples R ChinaKan, Anita S. Y.论文数: 0 引用数: 0 h-index: 0机构: Univ Hong Kong, Queen Mary Hosp, Dept Obstet & Gynaecol, Hong Kong, Hong Kong, Peoples R China Tsan Yuk Hosp, Dept Obstet & Gynaecol, Prenatal Diagnost Lab, Hong Kong, Hong Kong, Peoples R China Univ Hong Kong, LKS Fac Med, Dept Paediat & Adolescent Med, Room 103,1-F New Clin Bldg, Hong Kong, Hong Kong, Peoples R ChinaChung, Brian H. Y.论文数: 0 引用数: 0 h-index: 0机构: Univ Hong Kong, LKS Fac Med, Dept Paediat & Adolescent Med, Room 103,1-F New Clin Bldg, Hong Kong, Hong Kong, Peoples R China Univ Hong Kong, Queen Mary Hosp, Dept Obstet & Gynaecol, Hong Kong, Hong Kong, Peoples R China Tsan Yuk Hosp, Dept Obstet & Gynaecol, Prenatal Diagnost Lab, Hong Kong, Hong Kong, Peoples R China Univ Hong Kong, LKS Fac Med, Dept Paediat & Adolescent Med, Room 103,1-F New Clin Bldg, Hong Kong, Hong Kong, Peoples R China
- [9] Prenatal diagnosis by trio exome sequencing in fetuses with ultrasound anomalies: A powerful diagnostic toolFRONTIERS 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 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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
- [10] Ultrafast MRI of the fetus: an increasingly important tool in prenatal diagnosis of congenital anomaliesMAGNETIC RESONANCE IMAGING, 2010, 28 (10) : 1431 - 1439Hosny, Iman A.论文数: 0 引用数: 0 h-index: 0机构: Cairo Univ, Fac Med, Dept Radiodiag, Cairo, Egypt Cairo Univ, Fac Med, Dept Radiodiag, Cairo, EgyptElghawabi, Hamed S.论文数: 0 引用数: 0 h-index: 0机构: Cairo Univ, Fac Med, Dept Radiodiag, Cairo, Egypt Cairo Univ, Fac Med, Dept Radiodiag, Cairo, Egypt