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- [21] Arthrogryposis multiplex with deafness, inguinal hernias, and early death:: A family report of a probably autosomal recessive traitAMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2005, 137A (02) : 125 - 129Tiemann, C论文数: 0 引用数: 0 h-index: 0机构: Virchow Hosp, Charite Med Ctr, Dept Neonatol, Berlin, GermanyBührer, C论文数: 0 引用数: 0 h-index: 0机构: Virchow Hosp, Charite Med Ctr, Dept Neonatol, Berlin, GermanyBurwinkel, B论文数: 0 引用数: 0 h-index: 0机构: Virchow Hosp, Charite Med Ctr, Dept Neonatol, Berlin, GermanyWirtenberger, M论文数: 0 引用数: 0 h-index: 0机构: Virchow Hosp, Charite Med Ctr, Dept Neonatol, Berlin, GermanyHoehn, T论文数: 0 引用数: 0 h-index: 0机构: Virchow Hosp, Charite Med Ctr, Dept Neonatol, Berlin, GermanyHübner, C论文数: 0 引用数: 0 h-index: 0机构: Virchow Hosp, Charite Med Ctr, Dept Neonatol, Berlin, Germanyvan Landeghem, FKH论文数: 0 引用数: 0 h-index: 0机构: Virchow Hosp, Charite Med Ctr, Dept Neonatol, Berlin, GermanyStoltenburg, G论文数: 0 引用数: 0 h-index: 0机构: Virchow Hosp, Charite Med Ctr, Dept Neonatol, Berlin, GermanyObladen, M论文数: 0 引用数: 0 h-index: 0机构: Virchow Hosp, Charite Med Ctr, Dept Neonatol, Berlin, Germany
- [22] SCYL2-related autosomal recessive neurodevelopmental disorders: Arthrogryposis multiplex congenita-4 and beyond?CLINICAL GENETICS, 2024, 106 (06) : 757 - 763Malbos, Marlene论文数: 0 引用数: 0 h-index: 0机构: CHU Dijon Bourgogne, FHU TRANSLAD, CRMRs Anomalies Dev & Syndromes Malformat & Defic, Dijon, France CHU Dijon Bourgogne, Lab Genom Med, UF Innovat Diagnost Genom Malad Rares, Dijon, France CHU Dijon Bourgogne, FHU TRANSLAD, CRMRs Anomalies Dev & Syndromes Malformat & Defic, Dijon, FranceVera, Gabriella论文数: 0 引用数: 0 h-index: 0机构: Normandie Univ, Univ Rouen Normandie, INSERM, U1245,Dept Genet,Dept Pathol, Rouen, France Normandie Univ, Univ Rouen Normandie, Reference Ctr Dev Abnormal, Inserm,U1245, Rouen, France CHU Rouen, Rouen, France CHU Dijon Bourgogne, FHU TRANSLAD, CRMRs Anomalies Dev & Syndromes Malformat & Defic, Dijon, FranceSheth, Harsh论文数: 0 引用数: 0 h-index: 0机构: FRIGEs Inst Human Genet, Ahmadabad, Gujarat, India CHU Dijon Bourgogne, FHU TRANSLAD, CRMRs Anomalies Dev & Syndromes Malformat & Defic, Dijon, FranceSchnur, Rhonda E.论文数: 0 引用数: 0 h-index: 0机构: Rowan Univ, Cooper Univ Hlth Care, Cooper Med Sch, Camden, NJ USA CHU Dijon Bourgogne, FHU TRANSLAD, CRMRs Anomalies Dev & Syndromes Malformat & Defic, Dijon, FranceJuven, Aurelien论文数: 0 引用数: 0 h-index: 0机构: CHU Dijon Bourgogne, FHU TRANSLAD, CRMRs Anomalies Dev & Syndromes Malformat & Defic, Dijon, France CHU Dijon Bourgogne, Lab Genom Med, UF Innovat Diagnost Genom Malad Rares, Dijon, France CHU Dijon Bourgogne, FHU TRANSLAD, CRMRs Anomalies Dev & Syndromes Malformat & Defic, Dijon, FranceBrehin, Anne-Claire论文数: 0 引用数: 0 h-index: 0机构: Normandie Univ, Univ Rouen Normandie, INSERM, U1245,Dept Genet,Dept Pathol, Rouen, France Normandie Univ, Univ Rouen Normandie, Reference Ctr Dev Abnormal, Inserm,U1245, Rouen, France CHU Rouen, Rouen, France CHU Dijon Bourgogne, FHU TRANSLAD, CRMRs Anomalies Dev & Syndromes Malformat & Defic, Dijon, FranceSheth, Jayesh论文数: 0 引用数: 0 h-index: 0机构: FRIGEs Inst Human Genet, Ahmadabad, Gujarat, India CHU Dijon Bourgogne, FHU TRANSLAD, CRMRs Anomalies Dev & Syndromes Malformat & Defic, Dijon, FranceGandhi, Ajit论文数: 0 引用数: 0 h-index: 0机构: FRIGEs Inst Human Genet, Ahmadabad, Gujarat, India CHU Dijon Bourgogne, FHU TRANSLAD, CRMRs Anomalies Dev & Syndromes Malformat & Defic, Dijon, FranceShapiro, Faye L.论文数: 0 引用数: 0 h-index: 0机构: Rowan Univ, Cooper Univ Hlth Care, Cooper Med Sch, Camden, NJ USA CHU Dijon Bourgogne, FHU TRANSLAD, CRMRs Anomalies Dev & Syndromes Malformat & Defic, Dijon, FranceBruel, Ange-Line论文数: 0 引用数: 0 h-index: 0机构: CHU Dijon Bourgogne, Lab Genom Med, UF Innovat Diagnost Genom Malad Rares, Dijon, France Univ Bourgogne Franche Comte, INSERM, UMR1231, FHU TRANSLAD,GAD, Dijon, France CHU Dijon Bourgogne, FHU TRANSLAD, CRMRs Anomalies Dev & Syndromes Malformat & Defic, Dijon, France论文数: 引用数: h-index:机构:Begtrup, Amber论文数: 0 引用数: 0 h-index: 0机构: GeneDx, Gaithersburg, MD USA CHU Dijon Bourgogne, FHU TRANSLAD, CRMRs Anomalies Dev & Syndromes Malformat & Defic, Dijon, FranceMonaghan, Kristin G.论文数: 0 引用数: 0 h-index: 0机构: GeneDx, Gaithersburg, MD USA CHU Dijon Bourgogne, FHU TRANSLAD, CRMRs Anomalies Dev & Syndromes Malformat & Defic, Dijon, FranceSafraou, Hana论文数: 0 引用数: 0 h-index: 0机构: CHU Dijon Bourgogne, Lab Genom Med, UF Innovat Diagnost Genom Malad Rares, Dijon, France Univ Bourgogne Franche Comte, INSERM, UMR1231, FHU TRANSLAD,GAD, Dijon, France CHU Dijon Bourgogne, FHU TRANSLAD, CRMRs Anomalies Dev & Syndromes Malformat & Defic, Dijon, FranceBrasseur-Daudruy, Marie论文数: 0 引用数: 0 h-index: 0机构: CHU Rouen, Radiol Pediat, Rouen, France CHU Dijon Bourgogne, FHU TRANSLAD, CRMRs Anomalies Dev & Syndromes Malformat & Defic, Dijon, FranceMau-Them, Frederic Tran论文数: 0 引用数: 0 h-index: 0机构: CHU Dijon Bourgogne, Lab Genom Med, UF Innovat Diagnost Genom Malad Rares, Dijon, France Univ Bourgogne Franche Comte, INSERM, UMR1231, FHU TRANSLAD,GAD, Dijon, France CHU Dijon Bourgogne, FHU TRANSLAD, CRMRs Anomalies Dev & Syndromes Malformat & Defic, Dijon, FranceDuffourd, Yannis论文数: 0 引用数: 0 h-index: 0机构: CHU Dijon Bourgogne, Lab Genom Med, UF Innovat Diagnost Genom Malad Rares, Dijon, France CHU Dijon Bourgogne, FHU TRANSLAD, CRMRs Anomalies Dev & Syndromes Malformat & Defic, Dijon, FranceFaivre, Laurence论文数: 0 引用数: 0 h-index: 0机构: CHU Dijon Bourgogne, FHU TRANSLAD, CRMRs Anomalies Dev & Syndromes Malformat & Defic, Dijon, France CHU Dijon Bourgogne, Lab Genom Med, UF Innovat Diagnost Genom Malad Rares, Dijon, France CHU Dijon Bourgogne, FHU TRANSLAD, CRMRs Anomalies Dev & Syndromes Malformat & Defic, Dijon, FranceThauvin-Robinet, Christel论文数: 0 引用数: 0 h-index: 0机构: CHU Dijon Bourgogne, FHU TRANSLAD, CRMRs Anomalies Dev & Syndromes Malformat & Defic, Dijon, France CHU Dijon Bourgogne, Lab Genom Med, UF Innovat Diagnost Genom Malad Rares, Dijon, France CHU Dijon Bourgogne, FHU TRANSLAD, CRMRs Anomalies Dev & Syndromes Malformat & Defic, Dijon, FranceBenke, Paul J.论文数: 0 引用数: 0 h-index: 0机构: Joe DiMaggio Childrens Hosp, Div Clin Genet, Hollywood, FL USA CHU Dijon Bourgogne, FHU TRANSLAD, CRMRs Anomalies Dev & Syndromes Malformat & Defic, Dijon, FrancePhilippe, Christophe论文数: 0 引用数: 0 h-index: 0机构: CHU Dijon Bourgogne, Lab Genom Med, UF Innovat Diagnost Genom Malad Rares, Dijon, France Univ Bourgogne Franche Comte, INSERM, UMR1231, FHU TRANSLAD,GAD, Dijon, France CHR Metz Thionville, Hop Mercy, Lab Genet, Metz, France CHU Dijon Bourgogne, FHU TRANSLAD, CRMRs Anomalies Dev & Syndromes Malformat & Defic, Dijon, France
- [23] Biallelic variants in ADAMTS15 cause a novel form of distal arthrogryposisGENETICS IN MEDICINE, 2022, 24 (10) : 2187 - 2193Boschann, Felix论文数: 0 引用数: 0 h-index: 0机构: Charit Univ Med Berlin, Inst Med Genet & Human Genet, Berlin, Germany Free Univ Berlin, Berlin, Germany Humboldt Univ, Berlin, Germany Max Planck Inst Mol Genet, RG Dev & Dis, Berlin, Germany Charit Univ Med Berlin, Inst Med Genet & Human Genet, Berlin, GermanyCogulu, Muhsin O.论文数: 0 引用数: 0 h-index: 0机构: Ege Univ, Dept Pediat Genet, Fac Med, Izmir, Turkey Charit Univ Med Berlin, Inst Med Genet & Human Genet, Berlin, GermanyPehlivan, Davut论文数: 0 引用数: 0 h-index: 0机构: Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USA Texas Childrens Hosp, Jan & Dan Duncan Neurol Res Inst, Houston, TX 77030 USA Baylor Coll Med, Dept Pediat, Sect Pediat Neurol & Dev Neurosci, Houston, TX 77030 USA Charit Univ Med Berlin, Inst Med Genet & Human Genet, Berlin, GermanyBalachandran, Saranya论文数: 0 引用数: 0 h-index: 0机构: Univ Lubeck, Inst Human Genet, Lubeck, Germany Univ Kiel, Inst Human Genet, Kiel, Germany Charit Univ Med Berlin, Inst Med Genet & Human Genet, Berlin, GermanyVallecillo-Garcia, Pedro论文数: 0 引用数: 0 h-index: 0机构: Free Univ Berlin, Inst Biochem, Berlin, Germany Charit Univ Med Berlin, Inst Med Genet & Human Genet, Berlin, GermanyGrochowski, Christopher M.论文数: 0 引用数: 0 h-index: 0机构: Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USA Charit Univ Med Berlin, Inst Med Genet & Human Genet, Berlin, GermanyHansmeier, Nils R.论文数: 0 引用数: 0 h-index: 0机构: Charit Univ Med Berlin, Inst Med Genet & Human Genet, Berlin, Germany Free Univ Berlin, Berlin, Germany Humboldt Univ, Berlin, Germany Max Planck Inst Mol Genet, RG Dev & Dis, Berlin, Germany Charite Univ Med Berlin, BCRT, Berlin, Germany Berlin Inst Hlth, Berlin, Germany Charit Univ Med Berlin, Inst Med Genet & Human Genet, Berlin, GermanyAkdemir, Zeynep H. Coban论文数: 0 引用数: 0 h-index: 0机构: Univ Texas Houston, UTHlth Sch Publ Hlth, Dept Epidemiol Human Genet & Environm Sci, Houston, TX USA Charit Univ Med Berlin, Inst Med Genet & Human Genet, Berlin, GermanyPrada-Medina, Cesar A.论文数: 0 引用数: 0 h-index: 0机构: Max Planck Inst Mol Genet, RG Dev & Dis, Berlin, Germany Charit Univ Med Berlin, Inst Med Genet & Human Genet, Berlin, Germany论文数: 引用数: h-index:机构:Fischer-Zirnsak, Bjorn论文数: 0 引用数: 0 h-index: 0机构: Charit Univ Med Berlin, Inst Med Genet & Human Genet, Berlin, Germany Free Univ Berlin, Berlin, Germany Humboldt Univ, Berlin, Germany Max Planck Inst Mol Genet, RG Dev & Dis, Berlin, Germany Charit Univ Med Berlin, Inst Med Genet & Human Genet, Berlin, GermanyBadura, Simon论文数: 0 引用数: 0 h-index: 0机构: Univ Med Ctr Gottingen, Dept Pediat & Adolescent Med, Interdisciplinary Pediat Ctr Children Dev Disabil, Gottingen, Germany Charit Univ Med Berlin, Inst Med Genet & Human Genet, Berlin, GermanyDurmaz, Burak论文数: 0 引用数: 0 h-index: 0机构: Ege Univ, Dept Pediat Genet, Fac Med, Izmir, Turkey Charit Univ Med Berlin, Inst Med Genet & Human Genet, Berlin, GermanyOzkinay, Ferda论文数: 0 引用数: 0 h-index: 0机构: Ege Univ, Fac Med, Dept Med Genet, Izmir, Turkey Charit Univ Med Berlin, Inst Med Genet & Human Genet, Berlin, GermanyHaegerling, Rene论文数: 0 引用数: 0 h-index: 0机构: Charit Univ Med Berlin, Inst Med Genet & Human Genet, Berlin, Germany Free Univ Berlin, Berlin, Germany Humboldt Univ, Berlin, Germany Max Planck Inst Mol Genet, RG Dev & Dis, Berlin, Germany Charite Univ Med Berlin, BCRT, Berlin, Germany Berlin Inst Hlth, Berlin, Germany Charit Univ Med Berlin, Inst Med Genet & Human Genet, Berlin, GermanyPosey, Jennifer E.论文数: 0 引用数: 0 h-index: 0机构: Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USA Charit Univ Med Berlin, Inst Med Genet & Human Genet, Berlin, GermanyStricker, Sigmar论文数: 0 引用数: 0 h-index: 0机构: Free Univ Berlin, Inst Biochem, Berlin, Germany Charit Univ Med Berlin, Inst Med Genet & Human Genet, Berlin, GermanyGillessen-Kaesbach, Gabriele论文数: 0 引用数: 0 h-index: 0机构: Univ Lubeck, Inst Human Genet, Lubeck, Germany Charit Univ Med Berlin, Inst Med Genet & Human Genet, Berlin, Germany论文数: 引用数: h-index:机构:Horn, Denise论文数: 0 引用数: 0 h-index: 0机构: Charit Univ Med Berlin, Inst Med Genet & Human Genet, Berlin, Germany Free Univ Berlin, Berlin, Germany Humboldt Univ, Berlin, Germany Charit Univ Med Berlin, Inst Med Genet & Human Genet, Berlin, GermanyBrockmann, Knut论文数: 0 引用数: 0 h-index: 0机构: Univ Med Ctr Gottingen, Dept Pediat & Adolescent Med, Interdisciplinary Pediat Ctr Children Dev Disabil, Gottingen, Germany Charit Univ Med Berlin, Inst Med Genet & Human Genet, Berlin, GermanyLupski, James R.论文数: 0 引用数: 0 h-index: 0机构: Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USA Texas Childrens Hosp, Jan & Dan Duncan Neurol Res Inst, Houston, TX 77030 USA Charit Univ Med Berlin, Inst Med Genet & Human Genet, Berlin, GermanyKornak, Uwe论文数: 0 引用数: 0 h-index: 0机构: Charit Univ Med Berlin, Inst Med Genet & Human Genet, Berlin, Germany Free Univ Berlin, Berlin, Germany Humboldt Univ, Berlin, Germany Max Planck Inst Mol Genet, RG Dev & Dis, Berlin, Germany Univ Med Ctr Gottingen, Inst Human Genet, Heinrich Duker Weg 12, D-37073 Gottingen, Germany Charit Univ Med Berlin, Inst Med Genet & Human Genet, Berlin, GermanySchmidt, Julia论文数: 0 引用数: 0 h-index: 0机构: Univ Lubeck, Inst Human Genet, Lubeck, Germany Univ Med Ctr Gottingen, Inst Human Genet, Heinrich Duker Weg 12, D-37073 Gottingen, Germany Charit Univ Med Berlin, Inst Med Genet & Human Genet, Berlin, Germany
- [24] Homozygous loss-of-function variants in FILIP1 cause autosomal recessive arthrogryposis multiplex congenita with microcephalyHuman Genetics, 2023, 142 : 543 - 552Franziska Schnabel论文数: 0 引用数: 0 h-index: 0机构: University Medical Center Göttingen,Institute of Human GeneticsElisabeth Schuler论文数: 0 引用数: 0 h-index: 0机构: University Medical Center Göttingen,Institute of Human GeneticsAlmundher Al-Maawali论文数: 0 引用数: 0 h-index: 0机构: University Medical Center Göttingen,Institute of Human GeneticsAnkur Chaurasia论文数: 0 引用数: 0 h-index: 0机构: University Medical Center Göttingen,Institute of Human GeneticsSteffen Syrbe论文数: 0 引用数: 0 h-index: 0机构: University Medical Center Göttingen,Institute of Human GeneticsAdila Al-Kindi论文数: 0 引用数: 0 h-index: 0机构: University Medical Center Göttingen,Institute of Human GeneticsGandham SriLakshmi Bhavani论文数: 0 引用数: 0 h-index: 0机构: University Medical Center Göttingen,Institute of Human GeneticsAnju Shukla论文数: 0 引用数: 0 h-index: 0机构: University Medical Center Göttingen,Institute of Human GeneticsJanine Altmüller论文数: 0 引用数: 0 h-index: 0机构: University Medical Center Göttingen,Institute of Human GeneticsPeter Nürnberg论文数: 0 引用数: 0 h-index: 0机构: University Medical Center Göttingen,Institute of Human GeneticsSiddharth Banka论文数: 0 引用数: 0 h-index: 0机构: University Medical Center Göttingen,Institute of Human GeneticsKatta M. Girisha论文数: 0 引用数: 0 h-index: 0机构: University Medical Center Göttingen,Institute of Human GeneticsYun Li论文数: 0 引用数: 0 h-index: 0机构: University Medical Center Göttingen,Institute of Human GeneticsBernd Wollnik论文数: 0 引用数: 0 h-index: 0机构: University Medical Center Göttingen,Institute of Human GeneticsGökhan Yigit论文数: 0 引用数: 0 h-index: 0机构: University Medical Center Göttingen,Institute of Human Genetics
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