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Novel Exonic Deletions in TTC7A in a Newborn with Multiple Intestinal Atresia and Combined Immunodeficiency.
Saunders, Jessica R; Lehman, Anna; Turvey, Stuart E; Pan, Jie; Rajcan-Separovic, Evica; Muise, Aleixo M; Bush, Jonathan W.
Afiliação
  • Saunders JR; Department of Pathology and Laboratory Medicine, The University of British Columbia, 10125-2775 Laurel St., Vancouver, BC, V5Z 1M9, Canada.
  • Lehman A; Department of Medical Genetics, British Columbia Children's and Women's Hospital, The University of British Columbia, 4480 Oak St., Vancouver, BC, V6H 3N1, Canada.
  • Turvey SE; Department of Pediatrics, British Columbia Children's Hospital, The University of British Columbia, 4480 Oak St., Vancouver, BC, V6H3Na, Canada.
  • Pan J; SickKids Inflammatory Bowel Disease Center and Cell Biology Program Research Institute, The Hospital for Sick Children, 555 University Avenue, Toronto, ON, M5G 1X8, Canada.
  • Rajcan-Separovic E; Department of Pathology and Laboratory Medicine, British Columbia Children's and Women's Hospital, The University of British Columbia, 4480 Oak St, Vancouver, BC, V6H3N1, Canada.
  • Muise AM; SickKids Inflammatory Bowel Disease Center and Cell Biology Program Research Institute, The Hospital for Sick Children, 555 University Avenue, Toronto, ON, M5G 1X8, Canada.
  • Bush JW; Departments of Pediatrics, Institute of Medical Science and Biochemistry, The University of Toronto, Toronto, ON, Canada.
J Clin Immunol ; 39(6): 616-619, 2019 08.
Article em En | MEDLINE | ID: mdl-31342292
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Proteínas / Éxons / Imunodeficiência Combinada Severa / Deleção de Sequência / Atresia Intestinal Tipo de estudo: Prognostic_studies Limite: Humans / Male / Newborn Idioma: En Revista: J Clin Immunol Ano de publicação: 2019 Tipo de documento: Article País de afiliação: Canadá
Texto completo
Adicionar na Minha BVS
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Proteínas / Éxons / Imunodeficiência Combinada Severa / Deleção de Sequência / Atresia Intestinal Tipo de estudo: Prognostic_studies Limite: Humans / Male / Newborn Idioma: En Revista: J Clin Immunol Ano de publicação: 2019 Tipo de documento: Article País de afiliação: Canadá