[Genetic screening in early diagnosis of neonatal WAS gene-related disorders].

Liu, X; Yang, L; Wang, X C; Wu, B B; Wang, H J; Wang, H S; Qian, X W; Cheng, G Q; Cao, Y; Sun, J Q; Zhou, W H

Liu, X; Yang, L; Wang, X C; Wu, B B; Wang, H J; Wang, H S; Qian, X W; Cheng, G Q; Cao, Y; Sun, J Q; Zhou, W H.

Afiliação

Liu X; Department of Neonatology, Children's Hospital of Fudan University, Shanghai 201102, China.
Yang L; Translational Medicine Center of Children's Hospital of Fudan University, Shanghai 201102, China.
Wang XC; Department of Clinical Immunology, Children's Hospital of Fudan University, Shanghai 201102, China.
Wu BB; Translational Medicine Center of Children's Hospital of Fudan University, Shanghai 201102, China.
Wang HJ; Translational Medicine Center of Children's Hospital of Fudan University, Shanghai 201102, China.
Wang HS; Department of Hematology and Oncology, Children's Hospital of Fudan University, Shanghai 201102, China.
Qian XW; Department of Hematology and Oncology, Children's Hospital of Fudan University, Shanghai 201102, China.
Cheng GQ; Department of Neonatology, Children's Hospital of Fudan University, Shanghai 201102, China.
Cao Y; Department of Neonatology, Children's Hospital of Fudan University, Shanghai 201102, China.
Sun JQ; Department of Clinical Immunology, Children's Hospital of Fudan University, Shanghai 201102, China.
Zhou WH; Department of Neonatology, Children's Hospital of Fudan University, Shanghai 201102, China.

Zhonghua Er Ke Za Zhi ; 57(6): 429-433, 2019 Jun 02.

Article em Zh | MEDLINE | ID: mdl-31216799

Assuntos

Doenças Genéticas Ligadas ao Cromossomo X; Testes Genéticos/métodos; Trombocitopenia/diagnóstico; Proteína da Síndrome de Wiskott-Aldrich/genética; Síndrome de Wiskott-Aldrich/diagnóstico; Criança; Análise Mutacional de DNA; Diagnóstico Precoce; Humanos; Recém-Nascido; Masculino; Mutação; Estudos Retrospectivos; Trombocitopenia/genética; Síndrome de Wiskott-Aldrich/genética

Palavras-chave

Genes; Infant, newborn; Wiskott-Aldrich syndrome

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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Trombocitopenia / Síndrome de Wiskott-Aldrich / Testes Genéticos / Doenças Genéticas Ligadas ao Cromossomo X / Proteína da Síndrome de Wiskott-Aldrich Tipo de estudo: Diagnostic_studies / Observational_studies / Prognostic_studies / Risk_factors_studies / Screening_studies Limite: Child / Humans / Male / Newborn Idioma: Zh Revista: Zhonghua Er Ke Za Zhi Ano de publicação: 2019 Tipo de documento: Article País de afiliação: China País de publicação: China

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