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Mutations in the Epithelial Cadherin-p120-Catenin Complex Cause Mendelian Non-Syndromic Cleft Lip with or without Cleft Palate.
Cox, Liza L; Cox, Timothy C; Moreno Uribe, Lina M; Zhu, Ying; Richter, Chika T; Nidey, Nichole; Standley, Jennifer M; Deng, Mei; Blue, Elizabeth; Chong, Jessica X; Yang, Yueqin; Carstens, Russ P; Anand, Deepti; Lachke, Salil A; Smith, Joshua D; Dorschner, Michael O; Bedell, Bruce; Kirk, Edwin; Hing, Anne V; Venselaar, Hanka; Valencia-Ramirez, Luz C; Bamshad, Michael J; Glass, Ian A; Cooper, Jonathan A; Haan, Eric; Nickerson, Deborah A; van Bokhoven, Hans; Zhou, Huiqing; Krahn, Katy N; Buckley, Michael F; Murray, Jeffrey C; Lidral, Andrew C; Roscioli, Tony.
Afiliação
  • Cox LL; Division of Craniofacial Medicine, Department of Pediatrics, University of Washington, Seattle, WA 98195, USA; Center for Developmental Biology & Regenerative Medicine, Seattle Children's Research Institute, Seattle, WA 98101, USA; Division of Basic Sciences, Fred Hutchinson Cancer Research Cent
  • Cox TC; Division of Craniofacial Medicine, Department of Pediatrics, University of Washington, Seattle, WA 98195, USA; Center for Developmental Biology & Regenerative Medicine, Seattle Children's Research Institute, Seattle, WA 98101, USA; Department of Anatomy & Developmental Biology, Monash Univer
  • Moreno Uribe LM; Department of Orthodontics & the Iowa Institute for Oral Health Research, University of Iowa, Iowa City, IA 52242, USA.
  • Zhu Y; New South Wales Health Pathology, Prince of Wales Hospital, Randwick, NSW 2031, Australia; Genetics of Learning Disability Service, Waratah, NSW 2298, Australia.
  • Richter CT; Department of Orthodontics & the Iowa Institute for Oral Health Research, University of Iowa, Iowa City, IA 52242, USA.
  • Nidey N; Department of Pediatrics, University of Iowa, Iowa City, IA 52242, USA.
  • Standley JM; Department of Pediatrics, University of Iowa, Iowa City, IA 52242, USA.
  • Deng M; Birth Defects Research Laboratory, University of Washington, Seattle, WA 98195, USA.
  • Blue E; Division of Medical Genetics, Department of Medicine, University of Washington, Seattle, WA 98195, USA.
  • Chong JX; Division of Genetic Medicine, Department of Pediatrics, University of Washington, Seattle, WA 98195, USA.
  • Yang Y; Department of Medicine, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA 19104, USA.
  • Carstens RP; Department of Medicine, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA 19104, USA; Department of Genetics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA 19104, USA.
  • Anand D; Department of Biological Sciences, University of Delaware, Newark, DE 19716, USA.
  • Lachke SA; Department of Biological Sciences, University of Delaware, Newark, DE 19716, USA.
  • Smith JD; Department of Genome Sciences, University of Washington, Seattle, WA 98195, USA.
  • Dorschner MO; Northwest Clinical Genomics Laboratory, Center for Precision Diagnostics, University of Washington, Seattle, WA 98195, USA; Department of Pathology, University of Washington, Seattle, WA 98195, USA.
  • Bedell B; Department of Pediatrics, University of Iowa, Iowa City, IA 52242, USA.
  • Kirk E; New South Wales Health Pathology, Prince of Wales Hospital, Randwick, NSW 2031, Australia; Centre for Clinical Genetics, Sydney Children's Hospital, Randwick, Sydney, NSW 2031, Australia.
  • Hing AV; Division of Craniofacial Medicine, Department of Pediatrics, University of Washington, Seattle, WA 98195, USA; Seattle Craniofacial Center, Seattle Children's Hospital, Seattle, WA 98105, USA.
  • Venselaar H; Centre for Molecular and Biomolecular Informatics, Radboud University Nijmegen Medical Centre, Nijmegen 6500 HB, the Netherlands.
  • Valencia-Ramirez LC; Fundación Clínica Noel, Medellin 050021, Colombia.
  • Bamshad MJ; Division of Genetic Medicine, Department of Pediatrics, University of Washington, Seattle, WA 98195, USA; Department of Genome Sciences, University of Washington, Seattle, WA 98195, USA.
  • Glass IA; Birth Defects Research Laboratory, University of Washington, Seattle, WA 98195, USA; Division of Genetic Medicine, Department of Pediatrics, University of Washington, Seattle, WA 98195, USA.
  • Cooper JA; Division of Basic Sciences, Fred Hutchinson Cancer Research Center, Seattle, WA 98109, USA.
  • Haan E; South Australian Clinical Genetics Service, SA Pathology (at Women's and Children's Hospital), North Adelaide, SA 5006, Australia; School of Medicine, University of Adelaide, Adelaide, SA 5000, Australia.
  • Nickerson DA; Department of Genome Sciences, University of Washington, Seattle, WA 98195, USA.
  • van Bokhoven H; Department of Human Genetics, Radboud University Nijmegen Medical Centre, Nijmegen 6500 HB, the Netherlands; Department of Cognitive Neurosciences, Donders Institute for Brain, Cognition and Behaviour, Radboud University Medical Center, Nijmegen 6500 HB, the Netherlands.
  • Zhou H; Department of Human Genetics, Radboud University Nijmegen Medical Centre, Nijmegen 6500 HB, the Netherlands; Department of Molecular Developmental Biology, Radboud Institute for Molecular Life Sciences, Radboud University, Nijmegen 6525 GA, the Netherlands.
  • Krahn KN; UVA Center for Advanced Medical Analytics, School of Medicine, University of Virginia, Charlottesville, VA 22908, USA.
  • Buckley MF; New South Wales Health Pathology, Prince of Wales Hospital, Randwick, NSW 2031, Australia.
  • Murray JC; Department of Pediatrics, University of Iowa, Iowa City, IA 52242, USA.
  • Lidral AC; Lidral Orthodontics, Rockford, MI 49341, USA.
  • Roscioli T; Centre for Clinical Genetics, Sydney Children's Hospital, Randwick, Sydney, NSW 2031, Australia; Prince of Wales Clinical School, University of New South Wales, Randwick, NSW 2031, Australia; Neuroscience Research Australia, Sydney, NSW 2031, Australia. Electronic address: tony.roscioli@health.nsw.g
Am J Hum Genet ; 102(6): 1143-1157, 2018 06 07.
Article em En | MEDLINE | ID: mdl-29805042
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Caderinas / Fenda Labial / Fissura Palatina / Predisposição Genética para Doença / Cateninas / Mutação Tipo de estudo: Prognostic_studies Limite: Animals / Female / Humans / Infant / Male / Newborn Idioma: En Revista: Am J Hum Genet Ano de publicação: 2018 Tipo de documento: Article País de publicação: Estados Unidos
Texto completo
Adicionar na Minha BVS
Imprimir
XML
PubMed Links
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Caderinas / Fenda Labial / Fissura Palatina / Predisposição Genética para Doença / Cateninas / Mutação Tipo de estudo: Prognostic_studies Limite: Animals / Female / Humans / Infant / Male / Newborn Idioma: En Revista: Am J Hum Genet Ano de publicação: 2018 Tipo de documento: Article País de publicação: Estados Unidos