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3p14 deletion is a rare contiguous gene syndrome: report of 2 new patients and an overview of 14 patients.
Dimitrov, B I; Ogilvie, C; Wieczorek, D; Wakeling, E; Sikkema-Raddatz, B; van Ravenswaaij-Arts, C M A; Josifova, D.
Afiliação
  • Dimitrov BI; Department of Clinical Genetics, Guy's Hospital, London, United Kingdom.
  • Ogilvie C; Genetics Laboratories, Guy's Hospital, London, United Kingdom.
  • Wieczorek D; Institut für Humangenetik, Universitätsklinikum Essen, Universität Duisburg-Essen, Essen, Germany.
  • Wakeling E; North West Thames Regional Genetic Service, North West London Hospitals, NHS Trust, London, United Kingdom.
  • Sikkema-Raddatz B; Department of Genetics, University Medical Centre Groningen, University of Groningen, Groningen, The Netherlands.
  • van Ravenswaaij-Arts CM; Department of Genetics, University Medical Centre Groningen, University of Groningen, Groningen, The Netherlands.
  • Josifova D; Department of Clinical Genetics, Guy's Hospital, London, United Kingdom.
Am J Med Genet A ; 167(6): 1223-30, 2015 Jun.
Article em En | MEDLINE | ID: mdl-25908055
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Anormalidades Múltiplas / Cromossomos Humanos Par 3 / Deficiências do Desenvolvimento / Deleção Cromossômica Limite: Child / Child, preschool / Female / Humans / Infant / Male Idioma: En Ano de publicação: 2015 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Anormalidades Múltiplas / Cromossomos Humanos Par 3 / Deficiências do Desenvolvimento / Deleção Cromossômica Limite: Child / Child, preschool / Female / Humans / Infant / Male Idioma: En Ano de publicação: 2015 Tipo de documento: Article