Your browser doesn't support javascript.
loading
Orthopaedic manifestations within the 22q11.2 Deletion syndrome: A systematic review.
Homans, Jelle F; Tromp, Isabel N; Colo, Dino; Schlösser, Tom P C; Kruyt, Moyo C; Deeney, Vincent F X; Crowley, Terrence B; McDonald-McGinn, Donna M; Castelein, René M.
Afiliação
  • Homans JF; Department of Orthopaedic Surgery, University Medical Center Utrecht, Utrecht, The Netherlands.
  • Tromp IN; Department of Orthopaedic Surgery, University Medical Center Utrecht, Utrecht, The Netherlands.
  • Colo D; Department of Orthopaedic Surgery, University Medical Center Utrecht, Utrecht, The Netherlands.
  • Schlösser TPC; Department of Orthopaedic Surgery, University Medical Center Utrecht, Utrecht, The Netherlands.
  • Kruyt MC; Department of Orthopaedic Surgery, University Medical Center Utrecht, Utrecht, The Netherlands.
  • Deeney VFX; Department of Orthopaedic Surgery, The Children's Hospital of Philadelphia (CHOP) and The Perelman School of Medicine at the University of Pennsylvania, Philadelphia, Pennsylvania.
  • Crowley TB; Division of Human Genetics and 22q and You Center, The Children's Hospital of Philadelphia (CHOP), Philadelphia, Pennsylvania.
  • McDonald-McGinn DM; Division of Human Genetics and 22q and You Center, The Children's Hospital of Philadelphia (CHOP), Philadelphia, Pennsylvania.
  • Castelein RM; The Perelman School of Medicine at the University of Pennsylvania, Philadelphia, Pennsylvania.
Am J Med Genet A ; 176(10): 2104-2120, 2018 10.
Article em En | MEDLINE | ID: mdl-29159873
Assuntos
Palavras-chave
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Doenças Ósseas / Síndrome de DiGeorge Tipo de estudo: Diagnostic_studies / Guideline / Prevalence_studies / Systematic_reviews Limite: Humans Idioma: En Revista: Am J Med Genet A Assunto da revista: GENETICA MEDICA Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Holanda
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Doenças Ósseas / Síndrome de DiGeorge Tipo de estudo: Diagnostic_studies / Guideline / Prevalence_studies / Systematic_reviews Limite: Humans Idioma: En Revista: Am J Med Genet A Assunto da revista: GENETICA MEDICA Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Holanda