共 18 条
- [1] A human protein complex homologous to the Drosophila MSL complex is responsible for the majority of histone H4 acetylation at lysine 16MOLECULAR AND CELLULAR BIOLOGY, 2005, 25 (21) : 9175 - 9188Smith, ER论文数: 0 引用数: 0 h-index: 0机构: Emory Univ, Dept Biol, Atlanta, GA 30322 USACayrou, C论文数: 0 引用数: 0 h-index: 0机构: Emory Univ, Dept Biol, Atlanta, GA 30322 USAHuang, R论文数: 0 引用数: 0 h-index: 0机构: Emory Univ, Dept Biol, Atlanta, GA 30322 USALane, WS论文数: 0 引用数: 0 h-index: 0机构: Emory Univ, Dept Biol, Atlanta, GA 30322 USACôté, J论文数: 0 引用数: 0 h-index: 0机构: Emory Univ, Dept Biol, Atlanta, GA 30322 USALucchesi, JC论文数: 0 引用数: 0 h-index: 0机构: Emory Univ, Dept Biol, Atlanta, GA 30322 USA
- [2] The Drosophila MSL complex acetylates histone h4 at lysine 16, a chromatin modification linked to dosage compensationMOLECULAR AND CELLULAR BIOLOGY, 2000, 20 (01) : 312 - 318Smith, ER论文数: 0 引用数: 0 h-index: 0机构: Emory Univ, Dept Biol, Atlanta, GA 30322 USAPannuti, A论文数: 0 引用数: 0 h-index: 0机构: Emory Univ, Dept Biol, Atlanta, GA 30322 USAGu, WG论文数: 0 引用数: 0 h-index: 0机构: Emory Univ, Dept Biol, Atlanta, GA 30322 USASteurnagel, A论文数: 0 引用数: 0 h-index: 0机构: Emory Univ, Dept Biol, Atlanta, GA 30322 USACook, RG论文数: 0 引用数: 0 h-index: 0机构: Emory Univ, Dept Biol, Atlanta, GA 30322 USAAllis, CD论文数: 0 引用数: 0 h-index: 0机构: Emory Univ, Dept Biol, Atlanta, GA 30322 USALucchesi, JC论文数: 0 引用数: 0 h-index: 0机构: Emory Univ, Dept Biol, Atlanta, GA 30322 USA
- [3] Acetylation of yeast histone H4 lysine 16: A switch for protein interactions in heterochromatin and euchromatinCOLD SPRING HARBOR SYMPOSIA ON QUANTITATIVE BIOLOGY, 2004, 69 : 193 - 200Millar, CB论文数: 0 引用数: 0 h-index: 0机构: Univ Calif Los Angeles, Sch Med, Dept Biol Chem, Los Angeles, CA 90095 USA Univ Calif Los Angeles, Sch Med, Dept Biol Chem, Los Angeles, CA 90095 USAKurdistani, SK论文数: 0 引用数: 0 h-index: 0机构: Univ Calif Los Angeles, Sch Med, Dept Biol Chem, Los Angeles, CA 90095 USAGrunstein, M论文数: 0 引用数: 0 h-index: 0机构: Univ Calif Los Angeles, Sch Med, Dept Biol Chem, Los Angeles, CA 90095 USA
- [4] Acetylation of Yeast Histone H4 Lysine 16: A Switch for Protein Interactions in Heterochromatin and EuchromatinEPIGENETICS, 2004, 69 : 193 - 200Millar, C. B.论文数: 0 引用数: 0 h-index: 0机构: Univ Calif Los Angeles, Sch Med, Dept Biol Chem, Los Angeles, CA 90095 USA Univ Calif Los Angeles, Sch Med, Dept Biol Chem, Los Angeles, CA 90095 USAKurdistani, S. K.论文数: 0 引用数: 0 h-index: 0机构: Univ Calif Los Angeles, Sch Med, Dept Biol Chem, Los Angeles, CA 90095 USAGrunstein, M.论文数: 0 引用数: 0 h-index: 0机构: Univ Calif Los Angeles, Sch Med, Dept Biol Chem, Los Angeles, CA 90095 USA
- [5] De novo mutations in MSL3 cause an X-linked syndrome marked by impaired histone H4 lysine 16 acetylationNATURE GENETICS, 2018, 50 (10) : 1442 - +Basilicata, M. Felicia论文数: 0 引用数: 0 h-index: 0机构: Max Planck Inst Immunobiol & Epigenet, Freiburg, Germany Max Planck Inst Immunobiol & Epigenet, Freiburg, GermanyBruel, Ange-Line论文数: 0 引用数: 0 h-index: 0机构: Univ Bourgogne Franche Comte, Genet Dev Disorders, Inserm UMR GAD 1231, Dijon, France Univ Bourgogne Franche Comte, Ctr Reference Malad Rares Anomalies Dev & Syndrom, Dijon, France Max Planck Inst Immunobiol & Epigenet, Freiburg, GermanySemplicio, Giuseppe论文数: 0 引用数: 0 h-index: 0机构: Max Planck Inst Immunobiol & Epigenet, Freiburg, Germany Max Planck Inst Immunobiol & Epigenet, Freiburg, GermanyValsecchi, Claudia Isabelle Keller论文数: 0 引用数: 0 h-index: 0机构: Max Planck Inst Immunobiol & Epigenet, Freiburg, Germany Max Planck Inst Immunobiol & Epigenet, Freiburg, GermanyAktas, Tugce论文数: 0 引用数: 0 h-index: 0机构: Max Planck Inst Immunobiol & Epigenet, Freiburg, Germany Max Planck Inst Immunobiol & Epigenet, Freiburg, GermanyDuffourd, Yannis论文数: 0 引用数: 0 h-index: 0机构: Univ Bourgogne Franche Comte, Genet Dev Disorders, Inserm UMR GAD 1231, Dijon, France Univ Bourgogne Franche Comte, Ctr Reference Malad Rares Anomalies Dev & Syndrom, Dijon, France Max Planck Inst Immunobiol & Epigenet, Freiburg, GermanyRumpf, Tobias论文数: 0 引用数: 0 h-index: 0机构: Max Planck Inst Immunobiol & Epigenet, Freiburg, Germany Max Planck Inst Immunobiol & Epigenet, Freiburg, GermanyMorton, Jenny论文数: 0 引用数: 0 h-index: 0机构: Birmingham Womens Hosp NHS Fdn Trust, West Midlands Reg Clin Genet Serv, Birmingham, W Midlands, England Birmingham Womens Hosp NHS Fdn Trust, Birmingham Hlth Partners, Birmingham, W Midlands, England Max Planck Inst Immunobiol & Epigenet, Freiburg, GermanyBache, Iben论文数: 0 引用数: 0 h-index: 0机构: Copenhagen Univ Hosp, Rigshosp, Dept Clin Genet, Copenhagen, Denmark Univ Copenhagen, Wilhelm Johannsen Ctr Funct Genome Res, Dept Cellular & Mol Med, Copenhagen, Denmark Max Planck Inst Immunobiol & Epigenet, Freiburg, GermanySzymanski, Witold G.论文数: 0 引用数: 0 h-index: 0机构: Max Planck Inst Immunobiol & Epigenet, Freiburg, Germany Max Planck Inst Immunobiol & Epigenet, Freiburg, GermanyGilissen, Christian论文数: 0 引用数: 0 h-index: 0机构: Radboud Univ Nijmegen, Donders Inst Brain Cognit & Behav, Dept Human Genet, Med Ctr, Nijmegen, Netherlands Max Planck Inst Immunobiol & Epigenet, Freiburg, GermanyVanakker, Olivier论文数: 0 引用数: 0 h-index: 0机构: Ghent Univ Hosp, Ctr Med Genet, Ghent, Belgium Max Planck Inst Immunobiol & Epigenet, Freiburg, Germany论文数: 引用数: h-index:机构:Mittler, Gerhard论文数: 0 引用数: 0 h-index: 0机构: Max Planck Inst Immunobiol & Epigenet, Freiburg, Germany Max Planck Inst Immunobiol & Epigenet, Freiburg, GermanyVan Der Burgt, Ineke论文数: 0 引用数: 0 h-index: 0机构: Radboud Univ Nijmegen, Donders Inst Brain Cognit & Behav, Dept Human Genet, Med Ctr, Nijmegen, Netherlands Max Planck Inst Immunobiol & Epigenet, Freiburg, GermanyEl Chehadeh, Salima论文数: 0 引用数: 0 h-index: 0机构: Univ Bourgogne Franche Comte, Genet Dev Disorders, Inserm UMR GAD 1231, Dijon, France Univ Bourgogne Franche Comte, Ctr Reference Malad Rares Anomalies Dev & Syndrom, Dijon, France Hop Hautepierre, Serv Genet Med, Strasbourg, France Max Planck Inst Immunobiol & Epigenet, Freiburg, GermanyCho, Megan T.论文数: 0 引用数: 0 h-index: 0机构: GeneDx, Gaithersburg, MD USA Max Planck Inst Immunobiol & Epigenet, Freiburg, GermanyPfundt, Rolph论文数: 0 引用数: 0 h-index: 0机构: Radboud Univ Nijmegen, Donders Inst Brain Cognit & Behav, Dept Human Genet, Med Ctr, Nijmegen, Netherlands Max Planck Inst Immunobiol & Epigenet, Freiburg, GermanyTan, Tiong Yang论文数: 0 引用数: 0 h-index: 0机构: Univ Melbourne, Royal Childrens Hosp, Murdoch Childrens Res Inst, Victorian Clin Genet Serv,Dept Paediat, Parkville, Vic, Australia Max Planck Inst Immunobiol & Epigenet, Freiburg, GermanyKirchhoff, Maria论文数: 0 引用数: 0 h-index: 0机构: Copenhagen Univ Hosp, Rigshosp, Dept Clin Genet, Copenhagen, Denmark Max Planck Inst Immunobiol & Epigenet, Freiburg, GermanyMenten, Bjorn论文数: 0 引用数: 0 h-index: 0机构: Ghent Univ Hosp, Ctr Med Genet, Ghent, Belgium Max Planck Inst Immunobiol & Epigenet, Freiburg, GermanyVergult, Sarah论文数: 0 引用数: 0 h-index: 0机构: Ghent Univ Hosp, Ctr Med Genet, Ghent, Belgium Max Planck Inst Immunobiol & Epigenet, Freiburg, GermanyLindstrom, Kristin论文数: 0 引用数: 0 h-index: 0机构: Phoenix Childrens Hosp, Div Genet & Metab, Phoenix, AZ USA Max Planck Inst Immunobiol & Epigenet, Freiburg, GermanyReis, Andre论文数: 0 引用数: 0 h-index: 0机构: Friedrich Alexander Univ Erlangen Nurnberg, Inst Human Genet, Erlangen, Germany Max Planck Inst Immunobiol & Epigenet, Freiburg, GermanyJohnson, Diana S.论文数: 0 引用数: 0 h-index: 0机构: Sheffield Childrens NHS Fdn Trust, Clin Genet Serv, Sheffield, S Yorkshire, England Max Planck Inst Immunobiol & Epigenet, Freiburg, GermanyFryer, Alan论文数: 0 引用数: 0 h-index: 0机构: Liverpool Womens NHS Fdn Trust, Dept Clin Genet, Liverpool, Merseyside, England Max Planck Inst Immunobiol & Epigenet, Freiburg, GermanyMcKay, Victoria论文数: 0 引用数: 0 h-index: 0机构: Liverpool Womens NHS Fdn Trust, Dept Clin Genet, Liverpool, Merseyside, England Max Planck Inst Immunobiol & Epigenet, Freiburg, GermanyFisher, Richard B.论文数: 0 引用数: 0 h-index: 0机构: James Cook Univ Hosp, Northern Genet Serv, Teesside Genet Unit, Middlesbrough, Cleveland, England Max Planck Inst Immunobiol & Epigenet, Freiburg, GermanyThauvin-Robinet, Christel论文数: 0 引用数: 0 h-index: 0机构: Univ Bourgogne Franche Comte, Genet Dev Disorders, Inserm UMR GAD 1231, Dijon, France Univ Bourgogne Franche Comte, Ctr Reference Malad Rares Anomalies Dev & Syndrom, Dijon, France Max Planck Inst Immunobiol & Epigenet, Freiburg, GermanyFrancis, David论文数: 0 引用数: 0 h-index: 0机构: Royal Childrens Hosp, Murdoch Childrens Res Inst, Victorian Clin Genet Serv, Cytogenet Lab, Victoria, Australia Max Planck Inst Immunobiol & Epigenet, Freiburg, GermanyRoscioli, Tony论文数: 0 引用数: 0 h-index: 0机构: Neurosci Res Australia, Sydney, NSW, Australia Univ New South Wales, Prince Wales Clin Sch, Sydney, NSW, Australia Sydney Childrens Hosp, Dept Med Genet, Sydney, NSW, Australia Max Planck Inst Immunobiol & Epigenet, Freiburg, GermanyPajusalu, Sander论文数: 0 引用数: 0 h-index: 0机构: Univ Tartu, Tartu Univ Hosp, Dept Clin Genet, United Labs, Tartu, Estonia Univ Tartu, Inst Clin Med, Tartu, Estonia Max Planck Inst Immunobiol & Epigenet, Freiburg, GermanyRadtke, Kelly论文数: 0 引用数: 0 h-index: 0机构: Ambry Genet, Dept Clin Genom, Aliso Viejo, CA USA Max Planck Inst Immunobiol & Epigenet, Freiburg, GermanyGanesh, Jaya论文数: 0 引用数: 0 h-index: 0机构: Rowan Univ, Div Genet, Cooper Univ Hosp, Camden, NJ USA Rowan Univ, Cooper Med Sch, Camden, NJ USA Max Planck Inst Immunobiol & Epigenet, Freiburg, GermanyBrunner, Han G.论文数: 0 引用数: 0 h-index: 0机构: Radboud Univ Nijmegen, Donders Inst Brain Cognit & Behav, Dept Human Genet, Med Ctr, Nijmegen, Netherlands Maastricht Univ, Dept Clin Genet, Med Ctr, Maastricht, Netherlands Maastricht Univ, Sch Oncol & Dev Biol, Med Ctr, Maastricht, Netherlands Max Planck Inst Immunobiol & Epigenet, Freiburg, GermanyWilson, Meredith论文数: 0 引用数: 0 h-index: 0机构: Univ Sydney, Childrens Hosp Westmead, Dept Clin Genet, Discipline Genet Med, Sydney, NSW, Australia Univ Sydney, Childrens Hosp Westmead, Dept Clin Genet, Discipline Child & Adolescent Hlth, Sydney, NSW, Australia Max Planck Inst Immunobiol & Epigenet, Freiburg, GermanyFaivre, Laurence论文数: 0 引用数: 0 h-index: 0机构: Univ Bourgogne Franche Comte, Genet Dev Disorders, Inserm UMR GAD 1231, Dijon, France Univ Bourgogne Franche Comte, Ctr Reference Malad Rares Anomalies Dev & Syndrom, Dijon, France Max Planck Inst Immunobiol & Epigenet, Freiburg, GermanyKalscheuer, Vera M.论文数: 0 引用数: 0 h-index: 0机构: Max Planck Inst Mol Genet, Res Grp Dev & Dis, Berlin, Germany Max Planck Inst Immunobiol & Epigenet, Freiburg, GermanyThevenon, Julien论文数: 0 引用数: 0 h-index: 0机构: Univ Bourgogne Franche Comte, Genet Dev Disorders, Inserm UMR GAD 1231, Dijon, France Univ Bourgogne Franche Comte, Ctr Reference Malad Rares Anomalies Dev & Syndrom, Dijon, France Univ Grenoble Alpes, Inst Adv Biosci, U1209, CHU Grenoble,INSERM,CNRS UMR 5309, Grenoble, France Max Planck Inst Immunobiol & Epigenet, Freiburg, GermanyAkhtar, Asifa论文数: 0 引用数: 0 h-index: 0机构: Max Planck Inst Immunobiol & Epigenet, Freiburg, Germany Max Planck Inst Immunobiol & Epigenet, Freiburg, Germany
- [6] De novo mutations in MSL3 cause an X-linked syndrome marked by impaired histone H4 lysine 16 acetylationNature Genetics, 2018, 50 : 1442 - 1451M. Felicia Basilicata论文数: 0 引用数: 0 h-index: 0机构: Max Planck Institute of Immunobiology and Epigenetics,Inserm UMR 1231 GAD, Genetics of Developmental disorders and Centre de Référence Maladies Rares Anomalies du Développement et syndromes malformatifs FHU TRANSLADAnge-Line Bruel论文数: 0 引用数: 0 h-index: 0机构: Max Planck Institute of Immunobiology and Epigenetics,Inserm UMR 1231 GAD, Genetics of Developmental disorders and Centre de Référence Maladies Rares Anomalies du Développement et syndromes malformatifs FHU TRANSLADGiuseppe Semplicio论文数: 0 引用数: 0 h-index: 0机构: Max Planck Institute of Immunobiology and Epigenetics,Inserm UMR 1231 GAD, Genetics of Developmental disorders and Centre de Référence Maladies Rares Anomalies du Développement et syndromes malformatifs FHU TRANSLADClaudia Isabelle Keller Valsecchi论文数: 0 引用数: 0 h-index: 0机构: Max Planck Institute of Immunobiology and Epigenetics,Inserm UMR 1231 GAD, Genetics of Developmental disorders and Centre de Référence Maladies Rares Anomalies du Développement et syndromes malformatifs FHU TRANSLADTuğçe Aktaş论文数: 0 引用数: 0 h-index: 0机构: Max Planck Institute of Immunobiology and Epigenetics,Inserm UMR 1231 GAD, Genetics of Developmental disorders and Centre de Référence Maladies Rares Anomalies du Développement et syndromes malformatifs FHU TRANSLADYannis Duffourd论文数: 0 引用数: 0 h-index: 0机构: Max Planck Institute of Immunobiology and Epigenetics,Inserm UMR 1231 GAD, Genetics of Developmental disorders and Centre de Référence Maladies Rares Anomalies du Développement et syndromes malformatifs FHU TRANSLADTobias Rumpf论文数: 0 引用数: 0 h-index: 0机构: Max Planck Institute of Immunobiology and Epigenetics,Inserm UMR 1231 GAD, Genetics of Developmental disorders and Centre de Référence Maladies Rares Anomalies du Développement et syndromes malformatifs FHU TRANSLADJenny Morton论文数: 0 引用数: 0 h-index: 0机构: Max Planck Institute of Immunobiology and Epigenetics,Inserm UMR 1231 GAD, Genetics of Developmental disorders and Centre de Référence Maladies Rares Anomalies du Développement et syndromes malformatifs FHU TRANSLADIben Bache论文数: 0 引用数: 0 h-index: 0机构: Max Planck Institute of Immunobiology and Epigenetics,Inserm UMR 1231 GAD, Genetics of Developmental disorders and Centre de Référence Maladies Rares Anomalies du Développement et syndromes malformatifs FHU TRANSLADWitold G. Szymanski论文数: 0 引用数: 0 h-index: 0机构: Max Planck Institute of Immunobiology and Epigenetics,Inserm UMR 1231 GAD, Genetics of Developmental disorders and Centre de Référence Maladies Rares Anomalies du Développement et syndromes malformatifs FHU TRANSLADChristian Gilissen论文数: 0 引用数: 0 h-index: 0机构: Max Planck Institute of Immunobiology and Epigenetics,Inserm UMR 1231 GAD, Genetics of Developmental disorders and Centre de Référence Maladies Rares Anomalies du Développement et syndromes malformatifs FHU TRANSLADOlivier Vanakker论文数: 0 引用数: 0 h-index: 0机构: Max Planck Institute of Immunobiology and Epigenetics,Inserm UMR 1231 GAD, Genetics of Developmental disorders and Centre de Référence Maladies Rares Anomalies du Développement et syndromes malformatifs FHU TRANSLADKatrin Õunap论文数: 0 引用数: 0 h-index: 0机构: Max Planck Institute of Immunobiology and Epigenetics,Inserm UMR 1231 GAD, Genetics of Developmental disorders and Centre de Référence Maladies Rares Anomalies du Développement et syndromes malformatifs FHU TRANSLADGerhard Mittler论文数: 0 引用数: 0 h-index: 0机构: Max Planck Institute of Immunobiology and Epigenetics,Inserm UMR 1231 GAD, Genetics of Developmental disorders and Centre de Référence Maladies Rares Anomalies du Développement et syndromes malformatifs FHU TRANSLADIneke van der Burgt论文数: 0 引用数: 0 h-index: 0机构: Max Planck Institute of Immunobiology and Epigenetics,Inserm UMR 1231 GAD, Genetics of Developmental disorders and Centre de Référence Maladies Rares Anomalies du Développement et syndromes malformatifs FHU TRANSLADSalima El Chehadeh论文数: 0 引用数: 0 h-index: 0机构: Max Planck Institute of Immunobiology and Epigenetics,Inserm UMR 1231 GAD, Genetics of Developmental disorders and Centre de Référence Maladies Rares Anomalies du Développement et syndromes malformatifs FHU TRANSLADMegan T. Cho论文数: 0 引用数: 0 h-index: 0机构: Max Planck Institute of Immunobiology and Epigenetics,Inserm UMR 1231 GAD, Genetics of Developmental disorders and Centre de Référence Maladies Rares Anomalies du Développement et syndromes malformatifs FHU TRANSLADRolph Pfundt论文数: 0 引用数: 0 h-index: 0机构: Max Planck Institute of Immunobiology and Epigenetics,Inserm UMR 1231 GAD, Genetics of Developmental disorders and Centre de Référence Maladies Rares Anomalies du Développement et syndromes malformatifs FHU TRANSLADTiong Yang Tan论文数: 0 引用数: 0 h-index: 0机构: Max Planck Institute of Immunobiology and Epigenetics,Inserm UMR 1231 GAD, Genetics of Developmental disorders and Centre de Référence Maladies Rares Anomalies du Développement et syndromes malformatifs FHU TRANSLADMaria Kirchhoff论文数: 0 引用数: 0 h-index: 0机构: Max Planck Institute of Immunobiology and Epigenetics,Inserm UMR 1231 GAD, Genetics of Developmental disorders and Centre de Référence Maladies Rares Anomalies du Développement et syndromes malformatifs FHU TRANSLADBjörn Menten论文数: 0 引用数: 0 h-index: 0机构: Max Planck Institute of Immunobiology and Epigenetics,Inserm UMR 1231 GAD, Genetics of Developmental disorders and Centre de Référence Maladies Rares Anomalies du Développement et syndromes malformatifs FHU TRANSLADSarah Vergult论文数: 0 引用数: 0 h-index: 0机构: Max Planck Institute of Immunobiology and Epigenetics,Inserm UMR 1231 GAD, Genetics of Developmental disorders and Centre de Référence Maladies Rares Anomalies du Développement et syndromes malformatifs FHU TRANSLADKristin Lindstrom论文数: 0 引用数: 0 h-index: 0机构: Max Planck Institute of Immunobiology and Epigenetics,Inserm UMR 1231 GAD, Genetics of Developmental disorders and Centre de Référence Maladies Rares Anomalies du Développement et syndromes malformatifs FHU TRANSLADAndré Reis论文数: 0 引用数: 0 h-index: 0机构: Max Planck Institute of Immunobiology and Epigenetics,Inserm UMR 1231 GAD, Genetics of Developmental disorders and Centre de Référence Maladies Rares Anomalies du Développement et syndromes malformatifs FHU TRANSLADDiana S. Johnson论文数: 0 引用数: 0 h-index: 0机构: Max Planck Institute of Immunobiology and Epigenetics,Inserm UMR 1231 GAD, Genetics of Developmental disorders and Centre de Référence Maladies Rares Anomalies du Développement et syndromes malformatifs FHU TRANSLADAlan Fryer论文数: 0 引用数: 0 h-index: 0机构: Max Planck Institute of Immunobiology and Epigenetics,Inserm UMR 1231 GAD, Genetics of Developmental disorders and Centre de Référence Maladies Rares Anomalies du Développement et syndromes malformatifs FHU TRANSLADVictoria McKay论文数: 0 引用数: 0 h-index: 0机构: Max Planck Institute of Immunobiology and Epigenetics,Inserm UMR 1231 GAD, Genetics of Developmental disorders and Centre de Référence Maladies Rares Anomalies du Développement et syndromes malformatifs FHU TRANSLADRichard B. Fisher论文数: 0 引用数: 0 h-index: 0机构: Max Planck Institute of Immunobiology and Epigenetics,Inserm UMR 1231 GAD, Genetics of Developmental disorders and Centre de Référence Maladies Rares Anomalies du Développement et syndromes malformatifs FHU TRANSLADChristel Thauvin-Robinet论文数: 0 引用数: 0 h-index: 0机构: Max Planck Institute of Immunobiology and Epigenetics,Inserm UMR 1231 GAD, Genetics of Developmental disorders and Centre de Référence Maladies Rares Anomalies du Développement et syndromes malformatifs FHU TRANSLADDavid Francis论文数: 0 引用数: 0 h-index: 0机构: Max Planck Institute of Immunobiology and Epigenetics,Inserm UMR 1231 GAD, Genetics of Developmental disorders and Centre de Référence Maladies Rares Anomalies du Développement et syndromes malformatifs FHU TRANSLADTony Roscioli论文数: 0 引用数: 0 h-index: 0机构: Max Planck Institute of Immunobiology and Epigenetics,Inserm UMR 1231 GAD, Genetics of Developmental disorders and Centre de Référence Maladies Rares Anomalies du Développement et syndromes malformatifs FHU TRANSLADSander Pajusalu论文数: 0 引用数: 0 h-index: 0机构: Max Planck Institute of Immunobiology and Epigenetics,Inserm UMR 1231 GAD, Genetics of Developmental disorders and Centre de Référence Maladies Rares Anomalies du Développement et syndromes malformatifs FHU TRANSLADKelly Radtke论文数: 0 引用数: 0 h-index: 0机构: Max Planck Institute of Immunobiology and Epigenetics,Inserm UMR 1231 GAD, Genetics of Developmental disorders and Centre de Référence Maladies Rares Anomalies du Développement et syndromes malformatifs FHU TRANSLADJaya Ganesh论文数: 0 引用数: 0 h-index: 0机构: Max Planck Institute of Immunobiology and Epigenetics,Inserm UMR 1231 GAD, Genetics of Developmental disorders and Centre de Référence Maladies Rares Anomalies du Développement et syndromes malformatifs FHU TRANSLADHan G. Brunner论文数: 0 引用数: 0 h-index: 0机构: Max Planck Institute of Immunobiology and Epigenetics,Inserm UMR 1231 GAD, Genetics of Developmental disorders and Centre de Référence Maladies Rares Anomalies du Développement et syndromes malformatifs FHU TRANSLADMeredith Wilson论文数: 0 引用数: 0 h-index: 0机构: Max Planck Institute of Immunobiology and Epigenetics,Inserm UMR 1231 GAD, Genetics of Developmental disorders and Centre de Référence Maladies Rares Anomalies du Développement et syndromes malformatifs FHU TRANSLADLaurence Faivre论文数: 0 引用数: 0 h-index: 0机构: Max Planck Institute of Immunobiology and Epigenetics,Inserm UMR 1231 GAD, Genetics of Developmental disorders and Centre de Référence Maladies Rares Anomalies du Développement et syndromes malformatifs FHU TRANSLADVera M. Kalscheuer论文数: 0 引用数: 0 h-index: 0机构: Max Planck Institute of Immunobiology and Epigenetics,Inserm UMR 1231 GAD, Genetics of Developmental disorders and Centre de Référence Maladies Rares Anomalies du Développement et syndromes malformatifs FHU TRANSLADJulien Thevenon论文数: 0 引用数: 0 h-index: 0机构: Max Planck Institute of Immunobiology and Epigenetics,Inserm UMR 1231 GAD, Genetics of Developmental disorders and Centre de Référence Maladies Rares Anomalies du Développement et syndromes malformatifs FHU TRANSLADAsifa Akhtar论文数: 0 引用数: 0 h-index: 0机构: Max Planck Institute of Immunobiology and Epigenetics,Inserm UMR 1231 GAD, Genetics of Developmental disorders and Centre de Référence Maladies Rares Anomalies du Développement et syndromes malformatifs FHU TRANSLAD
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