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Single suture craniosynostosis: Identification of rare variants in genes associated with syndromic forms. Am J Med Genet A. 2018 Feb;176(2):290-300.
Clarke, C M; Fok, V T; Gustafson, J A; Smyth, M D; Timms, A E; Frazar, C D; Smith, J D; Birgfeld, C B; Lee, A; Ellenbogen, R G; Gruss, J S; Hopper, R A; Cunningham, M L.
Afiliación
  • Clarke CM; Center for Developmental Biology and Regenerative Medicine, Seattle Children's Research Institute, Seattle, Washington.
  • Fok VT; Center for Developmental Biology and Regenerative Medicine, Seattle Children's Research Institute, Seattle, Washington.
  • Gustafson JA; Center for Developmental Biology and Regenerative Medicine, Seattle Children's Research Institute, Seattle, Washington.
  • Smyth MD; Washington University Department of Neurosurgery, St. Louis, Missouri.
  • Timms AE; St. Louis Children's Hospital, St. Louis, Missouri.
  • Frazar CD; Center for Developmental Biology and Regenerative Medicine, Seattle Children's Research Institute, Seattle, Washington.
  • Smith JD; Department of Genome Sciences, University of Washington, Seattle, Washington.
  • Birgfeld CB; Department of Genome Sciences, University of Washington, Seattle, Washington.
  • Lee A; Division of Plastic Surgery, Department of Surgery, University of Washington School of Medicine, Seattle, Washington.
  • Ellenbogen RG; Division of Craniofacial and Plastic Surgery, Seattle Children's Hospital, Seattle, Washington.
  • Gruss JS; Seattle Children's Craniofacial Center, Seattle Children's Hospital, Seattle, Washington.
  • Hopper RA; Seattle Children's Craniofacial Center, Seattle Children's Hospital, Seattle, Washington.
  • Cunningham ML; Department of Neurological Surgery, University of Washington School of Medicine, Seattle, Washington.
Am J Med Genet A ; 176(11): 2522, 2018 11.
Article en En | MEDLINE | ID: mdl-30537273
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Diagnostic_studies / Risk_factors_studies Idioma: En Revista: Am J Med Genet A Asunto de la revista: GENETICA MEDICA Año: 2018 Tipo del documento: Article Pais de publicación: Estados Unidos
Texto completo
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Imprimir
XML
PubMed Links
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Diagnostic_studies / Risk_factors_studies Idioma: En Revista: Am J Med Genet A Asunto de la revista: GENETICA MEDICA Año: 2018 Tipo del documento: Article Pais de publicación: Estados Unidos