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- [21] 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
- [22] Accuracy of prenatal ultrasound in the diagnosis of corpus callosum anomaliesJOURNAL OF MATERNAL-FETAL & NEONATAL MEDICINE, 2021, 34 (03) : 439 - 444Santirocco, Maddalena论文数: 0 引用数: 0 h-index: 0机构: Univ Autonoma Barcelona, Hosp Univ Vall dHebron, Dept Maternal Fetal Med, Barcelona, Spain Univ Autonoma Barcelona, Hosp Univ Vall dHebron, Dept Maternal Fetal Med, Barcelona, SpainRodo, Carlota论文数: 0 引用数: 0 h-index: 0机构: Univ Autonoma Barcelona, Hosp Univ Vall dHebron, Dept Maternal Fetal Med, Barcelona, Spain Univ Autonoma Barcelona, Hosp Univ Vall dHebron, Dept Maternal Fetal Med, Barcelona, SpainIllescas, Tamara论文数: 0 引用数: 0 h-index: 0机构: Univ Autonoma Barcelona, Hosp Univ Vall dHebron, Dept Maternal Fetal Med, Barcelona, Spain Hosp Univ La Paz, Dept Obstet & Gynecol, Madrid, Spain Univ Autonoma Barcelona, Hosp Univ Vall dHebron, Dept Maternal Fetal Med, Barcelona, SpainVazquez, Elida论文数: 0 引用数: 0 h-index: 0机构: Hosp Univ Vall dHebron, Dept Paediat Radiol, Barcelona, Spain Univ Autonoma Barcelona, Hosp Univ Vall dHebron, Dept Maternal Fetal Med, Barcelona, SpainGarrido, Marta论文数: 0 引用数: 0 h-index: 0机构: Hosp Univ Vall dHebron, Dept Pathol, Barcelona, Spain Univ Autonoma Barcelona, Hosp Univ Vall dHebron, Dept Maternal Fetal Med, Barcelona, SpainHigueras, Teresa论文数: 0 引用数: 0 h-index: 0机构: Univ Autonoma Barcelona, Hosp Univ Vall dHebron, Dept Maternal Fetal Med, Barcelona, Spain Univ Autonoma Barcelona, Hosp Univ Vall dHebron, Dept Maternal Fetal Med, Barcelona, SpainArevalo, Silvia论文数: 0 引用数: 0 h-index: 0机构: Univ Autonoma Barcelona, Hosp Univ Vall dHebron, Dept Maternal Fetal Med, Barcelona, Spain Univ Autonoma Barcelona, Hosp Univ Vall dHebron, Dept Maternal Fetal Med, Barcelona, SpainMaiz, Nerea论文数: 0 引用数: 0 h-index: 0机构: Univ Autonoma Barcelona, Hosp Univ Vall dHebron, Dept Maternal Fetal Med, Barcelona, Spain Univ Autonoma Barcelona, Hosp Univ Vall dHebron, Dept Maternal Fetal Med, Barcelona, SpainCarreras, Elena论文数: 0 引用数: 0 h-index: 0机构: Univ Autonoma Barcelona, Hosp Univ Vall dHebron, Dept Maternal Fetal Med, Barcelona, Spain Univ Autonoma Barcelona, Hosp Univ Vall dHebron, Dept Maternal Fetal Med, Barcelona, Spain
- [23] Prenatal genetic testing in 19 fetuses with corpus callosum abnormalityJOURNAL OF CLINICAL LABORATORY ANALYSIS, 2021, 35 (11)She, Qin论文数: 0 引用数: 0 h-index: 0机构: Guangzhou Med Univ, Affiliated Hosp 6, Prenatal Diagnost Ctr, Qingyuan Peoples Hosp, Qingyuan, Peoples R China Guangzhou Med Univ, Affiliated Hosp 6, Prenatal Diagnost Ctr, Qingyuan Peoples Hosp, Qingyuan, Peoples R ChinaTang, Erfang论文数: 0 引用数: 0 h-index: 0机构: Guangzhou Med Univ, Affiliated Hosp 6, Prenatal Diagnost Ctr, Qingyuan Peoples Hosp, Qingyuan, Peoples R China Guangzhou Med Univ, Affiliated Hosp 6, Prenatal Diagnost Ctr, Qingyuan Peoples Hosp, Qingyuan, Peoples R ChinaPeng, Cui论文数: 0 引用数: 0 h-index: 0机构: Guangzhou Med Univ, Affiliated Hosp 6, Prenatal Diagnost Ctr, Qingyuan Peoples Hosp, Qingyuan, Peoples R China Guangzhou Med Univ, Affiliated Hosp 6, Prenatal Diagnost Ctr, Qingyuan Peoples Hosp, Qingyuan, Peoples R ChinaWang, Li论文数: 0 引用数: 0 h-index: 0机构: Guangzhou Med Univ, Affiliated Hosp 6, Prenatal Diagnost Ctr, Qingyuan Peoples Hosp, Qingyuan, Peoples R China Guangzhou Med Univ, Affiliated Hosp 6, Prenatal Diagnost Ctr, Qingyuan Peoples Hosp, Qingyuan, Peoples R ChinaWang, Dandan论文数: 0 引用数: 0 h-index: 0机构: Guangzhou Med Univ, Affiliated Hosp 6, Prenatal Diagnost Ctr, Qingyuan Peoples Hosp, Qingyuan, Peoples R China Guangzhou Med Univ, Affiliated Hosp 6, Prenatal Diagnost Ctr, Qingyuan Peoples Hosp, Qingyuan, Peoples R ChinaTan, Weihe论文数: 0 引用数: 0 h-index: 0机构: Guangzhou Med Univ, Affiliated Hosp 6, Prenatal Diagnost Ctr, Qingyuan Peoples Hosp, Qingyuan, Peoples R China Guangzhou Med Univ, Affiliated Hosp 6, Prenatal Diagnost Ctr, Qingyuan Peoples Hosp, Qingyuan, Peoples R China
- [24] Prenatal exome sequencing analysis in the clinical setting of fetuses with structural anomalies or increased nuchal translucencyGENETICS IN MEDICINE, 2022, 24 (03) : S301 - S301Lazar, Roni Zemet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 USAMeng, Linyan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 USALiu, Pengfei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 USADai, Hongzheng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 USAXia, Fan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 USAEng, Christine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 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 Obstet & Gynecol, Houston, TX 77030 USA Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USAVossaert, Liesbeth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 USA
- [25] Whole Exome Sequencing in a Population of Fetuses With Structural AnomaliesPRENATAL DIAGNOSIS, 2025, : 310 - 317Burrill, Natalie论文数: 0 引用数: 0 h-index: 0机构: Childrens Hosp Philadelphia, Div Human Genet, Philadelphia, PA 19104 USA Childrens Hosp Philadelphia, Div Human Genet, Philadelphia, PA 19104 USASchindewolf, Erica论文数: 0 引用数: 0 h-index: 0机构: Childrens Hosp Philadelphia, Undiagnosed Dis Program, Philadelphia, PA USA Childrens Hosp Philadelphia, Div Human Genet, Philadelphia, PA 19104 USAPilchman, Lisa论文数: 0 引用数: 0 h-index: 0机构: Childrens Hosp Philadelphia, Richard D Wood Jr Ctr Fetal Diag & Treatment, Philadelphia, PA USA Childrens Hosp Philadelphia, Div Human Genet, Philadelphia, PA 19104 USAWright, Renee论文数: 0 引用数: 0 h-index: 0机构: Childrens Hosp Philadelphia, Richard D Wood Jr Ctr Fetal Diag & Treatment, Philadelphia, PA USA Childrens Hosp Philadelphia, Div Human Genet, Philadelphia, PA 19104 USACrane, Haley论文数: 0 引用数: 0 h-index: 0机构: Childrens Hosp Philadelphia, Richard D Wood Jr Ctr Fetal Diag & Treatment, Philadelphia, PA USA Childrens Hosp Philadelphia, Div Human Genet, Philadelphia, PA 19104 USAGebb, Juliana论文数: 0 引用数: 0 h-index: 0机构: Childrens Hosp Philadelphia, Richard D Wood Jr Ctr Fetal Diag & Treatment, Philadelphia, PA USA Univ Penn, Perelman Sch Med, Dept Surg, Philadelphia, PA USA Childrens Hosp Philadelphia, Div Human Genet, Philadelphia, PA 19104 USAKhalek, Nahla论文数: 0 引用数: 0 h-index: 0机构: Childrens Hosp Philadelphia, Richard D Wood Jr Ctr Fetal Diag & Treatment, Philadelphia, PA USA Univ Penn, Perelman Sch Med, Dept Surg, Philadelphia, PA USA Childrens Hosp Philadelphia, Div Human Genet, Philadelphia, PA 19104 USASoni, Shelly论文数: 0 引用数: 0 h-index: 0机构: Childrens Hosp Philadelphia, Richard D Wood Jr Ctr Fetal Diag & Treatment, Philadelphia, PA USA Univ Penn, Perelman Sch Med, Dept Surg, Philadelphia, PA USA Childrens Hosp Philadelphia, Div Human Genet, Philadelphia, PA 19104 USATeefey, Christina Paidas论文数: 0 引用数: 0 h-index: 0机构: Childrens Hosp Philadelphia, Richard D Wood Jr Ctr Fetal Diag & Treatment, Philadelphia, PA USA Univ Penn, Perelman Sch Med, Dept Surg, Philadelphia, PA USA Childrens Hosp Philadelphia, Div Human Genet, Philadelphia, PA 19104 USAOliver, Edward R.论文数: 0 引用数: 0 h-index: 0机构: Childrens Hosp Philadelphia, Richard D Wood Jr Ctr Fetal Diag & Treatment, Philadelphia, PA USA Univ Penn, Perelman Sch Med, Dept Radiol, Philadelphia, PA USA Childrens Hosp Philadelphia, Div Human Genet, Philadelphia, PA 19104 USALinn, Rebecca论文数: 0 引用数: 0 h-index: 0机构: Childrens Hosp Philadelphia, Div Anat Pathol, Philadelphia, PA USA Univ Penn, Perelman Sch Med, Dept Pathol & Lab Med, Philadelphia, PA USA Childrens Hosp Philadelphia, Div Human Genet, Philadelphia, PA 19104 USAMoldenhauer, Julie S.论文数: 0 引用数: 0 h-index: 0机构: Childrens Hosp Philadelphia, Richard D Wood Jr Ctr Fetal Diag & Treatment, Philadelphia, PA USA Univ Penn, Perelman Sch Med, Dept Surg, Philadelphia, PA USA Childrens Hosp Philadelphia, Div Human Genet, Philadelphia, PA 19104 USA
- [26] Exome sequencing for prenatal diagnosis of fetuses with sonographic abnormalitiesPRENATAL DIAGNOSIS, 2015, 35 (10) : 1010 - 1017Drury, Suzanne论文数: 0 引用数: 0 h-index: 0机构: Great Ormond St Hosp Children NHS Fdn Trust, North East Thames Reg Genet Serv, London, England Great Ormond St Hosp Children NHS Fdn Trust, North East Thames Reg Genet Serv, London, EnglandWilliams, Hywel论文数: 0 引用数: 0 h-index: 0机构: UCL Inst Child Hlth, Genet & Genom Med, London, England Great Ormond St Hosp Children NHS Fdn Trust, North East Thames Reg Genet Serv, London, EnglandTrump, Natalie论文数: 0 引用数: 0 h-index: 0机构: Great Ormond St Hosp Children NHS Fdn Trust, North East Thames Reg Genet Serv, London, England Great Ormond St Hosp Children NHS Fdn Trust, North East Thames Reg Genet Serv, London, EnglandBoustred, Christopher论文数: 0 引用数: 0 h-index: 0机构: Great Ormond St Hosp Children NHS Fdn Trust, North East Thames Reg Genet Serv, London, England Great Ormond St Hosp Children NHS Fdn Trust, North East Thames Reg Genet Serv, London, EnglandLench, Nicholas论文数: 0 引用数: 0 h-index: 0机构: Great Ormond St Hosp Children NHS Fdn Trust, North East Thames Reg Genet Serv, London, England Great Ormond St Hosp Children NHS Fdn Trust, North East Thames Reg Genet Serv, London, EnglandScott, Richard H.论文数: 0 引用数: 0 h-index: 0机构: Great Ormond St Hosp Children NHS Fdn Trust, North East Thames Reg Genet Serv, London, England Great Ormond St Hosp Children NHS Fdn Trust, North East Thames Reg Genet Serv, London, EnglandChitty, Lyn S.论文数: 0 引用数: 0 h-index: 0机构: Great Ormond St Hosp Children NHS Fdn Trust, North East Thames Reg Genet Serv, London, England UCL Inst Child Hlth, Genet & Genom Med, London, England Great Ormond St Hosp Children NHS Fdn Trust, North East Thames Reg Genet Serv, London, England
- [27] Diagnostic yield of exome sequencing in prenatal agenesis of corpus callosum: systematic review and meta-analysisULTRASOUND IN OBSTETRICS & GYNECOLOGY, 2024, 63 (03) : 312 - 320Mustafa, H. J.论文数: 0 引用数: 0 h-index: 0机构: Indiana Univ Sch Med, Dept Obstet & Gynecol, Div Maternal Fetal Med, Indianapolis, IN USA Riley Children, Indianapolis, IN USA Indiana Univ, Hlth Fetal Ctr, Indianapolis, IN USA Div Maternal Fetal Med, 340 West 10th St,Fairbanks Hall,Suite 6200, Indianapolis, IN 46202 USA Riley Childrens, Fetal Ctr, 575 Riley Hosp Dr 4300, Indianapolis, IN 46202 USA Indiana Univ Hlth, 575 Riley Hosp Dr 4300, Indianapolis, IN 46202 USA Indiana Univ Sch Med, Dept Obstet & Gynecol, Div Maternal Fetal Med, Indianapolis, IN USABarbera, J. P.论文数: 0 引用数: 0 h-index: 0机构: Thomas Jefferson Univ, Sidney Kimmel Med Coll, Philadelphia, PA USA Indiana Univ Sch Med, Dept Obstet & Gynecol, Div Maternal Fetal Med, Indianapolis, IN USASambatur, E. V.论文数: 0 引用数: 0 h-index: 0机构: Houston Ctr Maternal Fetal Med, Res Div, Houston, TX USA Indiana Univ Sch Med, Dept Obstet & Gynecol, Div Maternal Fetal Med, Indianapolis, IN USAPagani, G.论文数: 0 引用数: 0 h-index: 0机构: ASST Papa Giovanni XXIII, Dept Obstet & Gynecol, Maternal Fetal Med Unit, Bergamo, Italy Indiana Univ Sch Med, Dept Obstet & Gynecol, Div Maternal Fetal Med, Indianapolis, IN USAYaron, Y.论文数: 0 引用数: 0 h-index: 0机构: Tel Aviv Sourasky Med Ctr, Genet Inst, Prenatal Genet Diag Unit, Tel Aviv, Israel Tel Aviv Univ, Sackler Fac Med, Tel Aviv, Israel Indiana Univ Sch Med, Dept Obstet & Gynecol, Div Maternal Fetal Med, Indianapolis, IN USABaptiste, C. D.论文数: 0 引用数: 0 h-index: 0机构: Columbia Univ, Med Ctr, Obstet & Gynecol, Reprod Genet, New York, NY USA Indiana Univ Sch Med, Dept Obstet & Gynecol, Div Maternal Fetal Med, Indianapolis, IN USAWapner, R. J.论文数: 0 引用数: 0 h-index: 0机构: Columbia Univ, Med Ctr, Obstet & Gynecol, Reprod Genet, New York, NY USA Indiana Univ Sch Med, Dept Obstet & Gynecol, Div Maternal Fetal Med, Indianapolis, IN USABrewer, C. J.论文数: 0 引用数: 0 h-index: 0机构: Cincinnati Childrens Hosp Med Ctr, Div Human Genet, Cincinnati, OH USA Indiana Univ Sch Med, Dept Obstet & Gynecol, Div Maternal Fetal Med, Indianapolis, IN USAKhalil, A.论文数: 0 引用数: 0 h-index: 0机构: Univ London, St Georges Univ Hosp NHS Fdn Trust, Fetal Med Unit, London, England St Georges Univ London, Mol & Clin Sci Res Inst, Vasc Biol Res Ctr, London, England Indiana Univ Sch Med, Dept Obstet & Gynecol, Div Maternal Fetal Med, Indianapolis, IN USA
- [28] Improvement of prenatal care in case of fetal anomaly of the corpus callosum using exome sequencing during the pregnancyEUROPEAN JOURNAL OF HUMAN GENETICS, 2020, 28 (SUPPL 1) : 142 - 142Heide, S.论文数: 0 引用数: 0 h-index: 0机构: Sorbonne Univ, Grp Hosp Pitie Salpetriere, APHP, Dept Genet,UF Genet Med & CRMR Deficience Intelle, Paris, France Sorbonne Univ, Grp Hosp Pitie Salpetriere, APHP, Dept Genet,UF Genet Med & CRMR Deficience Intelle, Paris, FranceSpentchian, M.论文数: 0 引用数: 0 h-index: 0机构: Sorbonne Univ, Grp Hosp Pitie Salpetriere, APHP, Dept Genet,UF Genet Med & CRMR Deficience Intelle, Paris, France Sorbonne Univ, Grp Hosp Pitie Salpetriere, APHP, Dept Genet,UF Genet Med & CRMR Deficience Intelle, Paris, FranceValence, S.论文数: 0 引用数: 0 h-index: 0机构: Sorbonne Univ, Hop Armand Trousseau, APHP, Serv Neurol Pediat, Paris, France Sorbonne Univ, Grp Hosp Pitie Salpetriere, APHP, Dept Genet,UF Genet Med & CRMR Deficience Intelle, Paris, FranceBuratti, J.论文数: 0 引用数: 0 h-index: 0机构: Sorbonne Univ, Grp Hosp Pitie Salpetriere, APHP, UF Genom Dev,Dept Genet, Paris, France Sorbonne Univ, Grp Hosp Pitie Salpetriere, APHP, Dept Genet,UF Genet Med & CRMR Deficience Intelle, Paris, FranceMach, C.论文数: 0 引用数: 0 h-index: 0机构: Sorbonne Univ, Grp Hosp Pitie Salpetriere, APHP, UF Genom Dev,Dept Genet, Paris, France Sorbonne Univ, Grp Hosp Pitie Salpetriere, APHP, Dept Genet,UF Genet Med & CRMR Deficience Intelle, Paris, FranceLejeune, E.论文数: 0 引用数: 0 h-index: 0机构: Sorbonne Univ, Grp Hosp Pitie Salpetriere, APHP, UF Genom Dev,Dept Genet, Paris, France Sorbonne Univ, Grp Hosp Pitie Salpetriere, APHP, Dept Genet,UF Genet Med & CRMR Deficience Intelle, Paris, FranceOlin, V.论文数: 0 引用数: 0 h-index: 0机构: Sorbonne Univ, Grp Hosp Pitie Salpetriere, APHP, UF Genom Dev,Dept Genet, Paris, France Sorbonne Univ, Grp Hosp Pitie Salpetriere, APHP, Dept Genet,UF Genet Med & CRMR Deficience Intelle, Paris, FranceMassimello, M.论文数: 0 引用数: 0 h-index: 0机构: Sorbonne Univ, Grp Hosp Pitie Salpetriere, APHP, Dept Genet,UF Genet Med & CRMR Deficience Intelle, Paris, France Sorbonne Univ, Grp Hosp Pitie Salpetriere, APHP, Dept Genet,UF Genet Med & CRMR Deficience Intelle, Paris, FranceGarel, C.论文数: 0 引用数: 0 h-index: 0机构: Sorbonne Univ, Hop Armand Trousseau, APHP, Serv Radiol Pediat, Paris, France Sorbonne Univ, Grp Hosp Pitie Salpetriere, APHP, Dept Genet,UF Genet Med & CRMR Deficience Intelle, Paris, FranceBlondiaux, E.论文数: 0 引用数: 0 h-index: 0机构: Sorbonne Univ, Hop Armand Trousseau, APHP, Serv Radiol Pediat, Paris, France Sorbonne Univ, Grp Hosp Pitie Salpetriere, APHP, Dept Genet,UF Genet Med & CRMR Deficience Intelle, Paris, FranceQuenum-Miraillet, G.论文数: 0 引用数: 0 h-index: 0机构: Sorbonne Univ, Hop Armand Trousseau, APHP, Serv Cytogenet,HUEP, Paris, France Sorbonne Univ, Grp Hosp Pitie Salpetriere, APHP, Dept Genet,UF Genet Med & CRMR Deficience Intelle, Paris, FranceChantot-Bastaraud, S.论文数: 0 引用数: 0 h-index: 0机构: Sorbonne Univ, Hop Armand Trousseau, APHP, Serv Cytogenet,HUEP, Paris, France Sorbonne Univ, Grp Hosp Pitie Salpetriere, APHP, Dept Genet,UF Genet Med & CRMR Deficience Intelle, Paris, FranceMilh, M.论文数: 0 引用数: 0 h-index: 0机构: Hop La Timone, APHM, Serv Neurol Pediat, Marseille, France Sorbonne Univ, Grp Hosp Pitie Salpetriere, APHP, Dept Genet,UF Genet Med & CRMR Deficience Intelle, Paris, FrancePortes, V. Des论文数: 0 引用数: 0 h-index: 0机构: Hosp Civils Lyon, Serv Neurol Pediat, Bron, France Sorbonne Univ, Grp Hosp Pitie Salpetriere, APHP, Dept Genet,UF Genet Med & CRMR Deficience Intelle, Paris, FranceSpodenkiewic, M.论文数: 0 引用数: 0 h-index: 0机构: CHU Reims, Serv Genet Clin, Reims, France Sorbonne Univ, Grp Hosp Pitie Salpetriere, APHP, Dept Genet,UF Genet Med & CRMR Deficience Intelle, Paris, FranceLayet, V.论文数: 0 引用数: 0 h-index: 0机构: Hop Havre, Serv Genet Clin, Le Havre, France Sorbonne Univ, Grp Hosp Pitie Salpetriere, APHP, Dept Genet,UF Genet Med & CRMR Deficience Intelle, Paris, FranceDard, R.论文数: 0 引用数: 0 h-index: 0机构: Hop Poissy, Serv Genet Clin, Poissy, France Sorbonne Univ, Grp Hosp Pitie Salpetriere, APHP, Dept Genet,UF Genet Med & CRMR Deficience Intelle, Paris, FranceMoutton, S.论文数: 0 引用数: 0 h-index: 0机构: CHU Dijon, Serv Genet Med, Ctr Reference Anomalies Dev, Dijon, France Sorbonne Univ, Grp Hosp Pitie Salpetriere, APHP, Dept Genet,UF Genet Med & CRMR Deficience Intelle, Paris, FranceGorce, M.论文数: 0 引用数: 0 h-index: 0机构: CHU Angers, Serv Genet Clin, Angers, France Sorbonne Univ, Grp Hosp Pitie Salpetriere, APHP, Dept Genet,UF Genet Med & CRMR Deficience Intelle, Paris, FranceNizon, M.论文数: 0 引用数: 0 h-index: 0机构: CHU Nantes, Serv Genet Clin, Nantes, France Sorbonne Univ, Grp Hosp Pitie Salpetriere, APHP, Dept Genet,UF Genet Med & CRMR Deficience Intelle, Paris, FranceMercier, S.论文数: 0 引用数: 0 h-index: 0机构: CHU Nantes, Serv Genet Clin, Nantes, France Sorbonne Univ, Grp Hosp Pitie Salpetriere, APHP, Dept Genet,UF Genet Med & CRMR Deficience Intelle, Paris, FranceVincent, M.论文数: 0 引用数: 0 h-index: 0机构: CHU Nantes, Serv Genet Clin, Nantes, France Sorbonne Univ, Grp Hosp Pitie Salpetriere, APHP, Dept Genet,UF Genet Med & CRMR Deficience Intelle, Paris, FranceBeneteau, C.论文数: 0 引用数: 0 h-index: 0机构: CHU Nantes, Serv Genet Clin, Nantes, France Sorbonne Univ, Grp Hosp Pitie Salpetriere, APHP, Dept Genet,UF Genet Med & CRMR Deficience Intelle, Paris, FranceJouannic, J.论文数: 0 引用数: 0 h-index: 0机构: Sorbonne Univ, Hop Armand Trousseau, APHP, Serv Med Foetale,HUEP, Paris, France Sorbonne Univ, Grp Hosp Pitie Salpetriere, APHP, Dept Genet,UF Genet Med & CRMR Deficience Intelle, Paris, FranceMoutard, M.论文数: 0 引用数: 0 h-index: 0机构: Sorbonne Univ, Hop Armand Trousseau, APHP, Serv Neurol Pediat, Paris, France Sorbonne Univ, Grp Hosp Pitie Salpetriere, APHP, Dept Genet,UF Genet Med & CRMR Deficience Intelle, Paris, FranceKeren, B.论文数: 0 引用数: 0 h-index: 0机构: Sorbonne Univ, Grp Hosp Pitie Salpetriere, APHP, UF Genom Dev,Dept Genet, Paris, France Sorbonne Univ, Grp Hosp Pitie Salpetriere, APHP, Dept Genet,UF Genet Med & CRMR Deficience Intelle, Paris, FranceHeron, D.论文数: 0 引用数: 0 h-index: 0机构: Sorbonne Univ, Grp Hosp Pitie Salpetriere, APHP, UF Genom Dev,Dept Genet, Paris, France Sorbonne Univ, Grp Hosp Pitie Salpetriere, APHP, Dept Genet,UF Genet Med & CRMR Deficience Intelle, Paris, France
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