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Mutations in GDF11 and the extracellular antagonist, Follistatin, as a likely cause of Mendelian forms of orofacial clefting in humans.
Cox, Timothy C; Lidral, Andrew C; McCoy, Jason C; Liu, Huan; Cox, Liza L; Zhu, Ying; Anderson, Ryan D; Moreno Uribe, Lina M; Anand, Deepti; Deng, Mei; Richter, Chika T; Nidey, Nichole L; Standley, Jennifer M; Blue, Elizabeth E; Chong, Jessica X; Smith, Joshua D; Kirk, Edwin P; Venselaar, Hanka; Krahn, Katy N; van Bokhoven, Hans; Zhou, Huiqing; Cornell, Robert A; Glass, Ian A; Bamshad, Michael J; Nickerson, Deborah A; Murray, Jeffrey C; Lachke, Salil A; Thompson, Thomas B; Buckley, Michael F; Roscioli, Tony.
Afiliação
  • Cox TC; Division of Craniofacial Medicine, Department of Pediatrics, University of Washington, Seattle, Washington.
  • Lidral AC; Center for Developmental Biology & Regenerative Medicine, Seattle Children's Research Institute, Seattle, Washington.
  • McCoy JC; Department of Oral & Craniofacial Science, School of Dentistry, University of Missouri-Kansas City, Kansas City, Missouri.
  • Liu H; Lidral Orthodontics, Rockford, Michigan.
  • Cox LL; Department of Molecular Genetics, Biochemistry, and Microbiology, University of Cincinnati, Cincinnati, Ohio.
  • Zhu Y; Department of Anatomy and Cell Biology and Anatomy, University of Iowa, Iowa City, Iowa.
  • Anderson RD; Division of Craniofacial Medicine, Department of Pediatrics, University of Washington, Seattle, Washington.
  • Moreno Uribe LM; Center for Developmental Biology & Regenerative Medicine, Seattle Children's Research Institute, Seattle, Washington.
  • Anand D; Department of Oral & Craniofacial Science, School of Dentistry, University of Missouri-Kansas City, Kansas City, Missouri.
  • Deng M; Division of Basic Sciences, Fred Hutchinson Cancer Research Center, Seattle, Washington.
  • Richter CT; New South Wales Health Pathology, Prince of Wales Hospital, Randwick, New South Wales, Australia.
  • Nidey NL; Genetics of Learning Disability Service, Hunter Genetics, Waratah, New South Wales, Australia.
  • Standley JM; Department of Oral & Craniofacial Science, School of Dentistry, University of Missouri-Kansas City, Kansas City, Missouri.
  • Blue EE; Department of Orthodontics & the Iowa Institute for Oral Health Research, University of Iowa, Iowa City, Iowa.
  • Chong JX; Department of Biological Sciences, University of Delaware, Newark, Delaware.
  • Smith JD; Birth Defects Research Laboratory, University of Washington, Seattle, Washington.
  • Kirk EP; Department of Orthodontics & the Iowa Institute for Oral Health Research, University of Iowa, Iowa City, Iowa.
  • Venselaar H; Department of Pediatrics, University of Iowa, Iowa City, Iowa.
  • Krahn KN; Department of Pediatrics, University of Iowa, Iowa City, Iowa.
  • van Bokhoven H; Division of Medical Genetics, Department of Medicine, University of Washington, Seattle, Washington.
  • Zhou H; Division of Genetic Medicine, Department of Pediatrics, University of Washington, Seattle, Washington.
  • Cornell RA; Department of Genome Sciences, University of Washington, Seattle, Washington.
  • Glass IA; New South Wales Health Pathology, Prince of Wales Hospital, Randwick, New South Wales, Australia.
  • Bamshad MJ; Centre for Clinical Genetics, Sydney Children's Hospital, New South Wales, Australia.
  • Nickerson DA; Centre for Molecular and Biomolecular Informatics, Radboud University Medical Centre, Nijmegen, The Netherlands.
  • Murray JC; UVA Center for Advanced Medical Analytics, School of Medicine, University of Virginia, Charlottesville, Virginia.
  • Lachke SA; Department of Human Genetics, Radboud University Medical Centre, Nijmegen, The Netherlands.
  • Thompson TB; Department of Cognitive Neurosciences, Donders Institute for Brain, Cognition and Behaviour, Radboud University Medical Center, Nijmegen, The Netherlands.
  • Buckley MF; Department of Human Genetics, Radboud University Medical Centre, Nijmegen, The Netherlands.
  • Roscioli T; Department of Molecular Developmental Biology, Radboud Institute for Molecular Life Sciences, Radboud University, Nijmegen, The Netherlands.
Hum Mutat ; 40(10): 1813-1825, 2019 10.
Article em En | MEDLINE | ID: mdl-31215115
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Fenda Labial / Proteínas Morfogenéticas Ósseas / Predisposição Genética para Doença / Folistatina / Fatores de Diferenciação de Crescimento / Estudos de Associação Genética / Mutação Tipo de estudo: Prognostic_studies Limite: Humans Idioma: En Revista: Hum Mutat Assunto da revista: GENETICA MEDICA Ano de publicação: 2019 Tipo de documento: Article País de publicação: Estados Unidos
Texto completo
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XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Fenda Labial / Proteínas Morfogenéticas Ósseas / Predisposição Genética para Doença / Folistatina / Fatores de Diferenciação de Crescimento / Estudos de Associação Genética / Mutação Tipo de estudo: Prognostic_studies Limite: Humans Idioma: En Revista: Hum Mutat Assunto da revista: GENETICA MEDICA Ano de publicação: 2019 Tipo de documento: Article País de publicação: Estados Unidos