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Clinical and Immunological Defects and Outcomes in Patients with Chromosome 22q11.2 Deletion Syndrome.
Yu, Hsin-Hui; Chien, Yin-Hsiu; Lu, Meng-Yao; Hu, Ya-Chiao; Lee, Jyh-Hong; Wang, Li-Chieh; Lin, Yu-Tsan; Yang, Yao-Hsu; Chiang, Bor-Luen.
Afiliação
  • Yu HH; Department of Paediatrics, National Taiwan University Children's Hospital, Taipei, Taiwan.
  • Chien YH; Department of Paediatrics, National Taiwan University Children's Hospital, Taipei, Taiwan.
  • Lu MY; Department of Medical Genetics, National Taiwan University Hospital, Taipei, Taiwan.
  • Hu YC; Department of Paediatrics, National Taiwan University Children's Hospital, Taipei, Taiwan.
  • Lee JH; Department of Paediatrics, National Taiwan University Children's Hospital, Taipei, Taiwan.
  • Wang LC; Department of Paediatrics, National Taiwan University Children's Hospital, Taipei, Taiwan.
  • Lin YT; Department of Paediatrics, National Taiwan University Children's Hospital, Taipei, Taiwan.
  • Yang YH; Department of Paediatrics, National Taiwan University Children's Hospital, Taipei, Taiwan.
  • Chiang BL; Department of Paediatrics, National Taiwan University Children's Hospital, Taipei, Taiwan.
J Clin Immunol ; 42(8): 1721-1729, 2022 11.
Article em En | MEDLINE | ID: mdl-35925483
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Síndrome de DiGeorge / Cardiopatias Congênitas / Linfopenia Tipo de estudo: Diagnostic_studies / Observational_studies / Prognostic_studies / Screening_studies Limite: Humans / Infant / Newborn Idioma: En Ano de publicação: 2022 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Síndrome de DiGeorge / Cardiopatias Congênitas / Linfopenia Tipo de estudo: Diagnostic_studies / Observational_studies / Prognostic_studies / Screening_studies Limite: Humans / Infant / Newborn Idioma: En Ano de publicação: 2022 Tipo de documento: Article