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Platelet findings in 22q11.2 deletion syndrome correlate with disease manifestations but do not correlate with GPIb surface expression.
Campbell, Ian M; Crowley, T Blaine; Jobaliya, Chintan; Bailey, Alice; McGinn, Daniel E; Gaiser, Kimberly; Bassett, Anne; Gur, Raquel E; Morrow, Bernice; Emanuel, Beverly S; Franco, Aime T; French, Deborah; Zackai, Elaine H; McDonald-McGinn, Donna M; Lambert, Michele P.
Afiliación
  • Campbell IM; Division of Human Genetics and 22q and You Center, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA.
  • Crowley TB; Department of Biomedical and Health Informatics, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA.
  • Jobaliya C; Division of Human Genetics and 22q and You Center, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA.
  • Bailey A; Department of Pathology and Laboratory Medicine, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA.
  • McGinn DE; Division of Human Genetics and 22q and You Center, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA.
  • Gaiser K; Division of Human Genetics and 22q and You Center, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA.
  • Bassett A; Division of Human Genetics and 22q and You Center, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA.
  • Gur RE; Department of Psychiatry, University of Toronto, Toronto, Ontario, Canada.
  • Morrow B; Department of Psychiatry, Perelman School of Medicine at the University of Pennsylvania, Philadelphia, Pennsylvania, USA.
  • Emanuel BS; Department of Medicine, Albert Einstein College of Medicine, Bronx, New York, USA.
  • Franco AT; Division of Human Genetics and 22q and You Center, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA.
  • French D; Department of Pediatrics, Perelman School of Medicine at the University of Pennsylvania, Philadelphia, Pennsylvania, USA.
  • Zackai EH; Division of Endocrinology, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA.
  • McDonald-McGinn DM; Department of Pathology and Laboratory Medicine, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA.
  • Lambert MP; Division of Human Genetics and 22q and You Center, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA.
Clin Genet ; 103(1): 109-113, 2023 01.
Article en En | MEDLINE | ID: mdl-36075864
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Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Síndrome de DiGeorge Tipo de estudio: Diagnostic_studies Límite: Humans Idioma: En Revista: Clin Genet Año: 2023 Tipo del documento: Article País de afiliación: Estados Unidos
Texto completo
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XML
PubMed Links
Buscar en Google

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Síndrome de DiGeorge Tipo de estudio: Diagnostic_studies Límite: Humans Idioma: En Revista: Clin Genet Año: 2023 Tipo del documento: Article País de afiliación: Estados Unidos