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Correction to: Genetics etiologies and genotype phenotype correlations in a cohort of individuals with central conducting lymphatic anomaly.
Liu, Mandi; Smith, Christopher L; Biko, David M; Li, Dong; Pinto, Erin; O'Connor, Nora; Skraban, Cara; Zackai, Elaine H; Hakonarson, Hakon; Dori, Yoav; Sheppard, Sarah E.
Afiliação
  • Liu M; Jill and Mark Fishman Center for Lymphatic Disorders, Children's Hospital of Philadelphia, Philadelphia, PA, USA.
  • Smith CL; Jill and Mark Fishman Center for Lymphatic Disorders, Children's Hospital of Philadelphia, Philadelphia, PA, USA.
  • Biko DM; Department of Radiology, Children's Hospital of Philadelphia, Philadelphia, PA, USA.
  • Li D; Center for Applied Genomics, Children's Hospital of Philadelphia, Philadelphia, PA, USA.
  • Pinto E; Division of Human Genetics, Children's Hospital of Philadelphia, Philadelphia, PA, USA.
  • O'Connor N; Jill and Mark Fishman Center for Lymphatic Disorders, Children's Hospital of Philadelphia, Philadelphia, PA, USA.
  • Skraban C; Center for Applied Genomics, Children's Hospital of Philadelphia, Philadelphia, PA, USA.
  • Zackai EH; Division of Human Genetics, Children's Hospital of Philadelphia, Philadelphia, PA, USA.
  • Hakonarson H; Division of Human Genetics, Children's Hospital of Philadelphia, Philadelphia, PA, USA.
  • Dori Y; Center for Applied Genomics, Children's Hospital of Philadelphia, Philadelphia, PA, USA.
  • Sheppard SE; Division of Human Genetics, Children's Hospital of Philadelphia, Philadelphia, PA, USA.
Eur J Hum Genet ; 30(9): 1094, 2022 Sep.
Article em En | MEDLINE | ID: mdl-35654890
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Texto completo: 1 Bases de dados: MEDLINE Tipo de estudo: Etiology_studies Idioma: En Revista: Eur J Hum Genet Assunto da revista: GENETICA MEDICA Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Estados Unidos
Texto completo
Adicionar na Minha BVS
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Bases de dados: MEDLINE Tipo de estudo: Etiology_studies Idioma: En Revista: Eur J Hum Genet Assunto da revista: GENETICA MEDICA Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Estados Unidos