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New Genotypes and Phenotypes in Patients with 3 Subtypes of Waardenburg Syndrome Identified by Diagnostic Next-Generation Sequencing.
Li, Wu; Mei, Lingyun; Chen, Hongsheng; Cai, Xinzhang; Liu, Yalan; Men, Meichao; Liu, Xue Zhong; Yan, Denise; Ling, Jie; Feng, Yong.
Afiliação
  • Li W; Department of Otolaryngology, Xiangya Hospital, Central South University, 87 Xiangya Road, Changsha, Hunan, China.
  • Mei L; Province Key Laboratory of Otolaryngology Critical Diseases, Changsha, Hunan, China.
  • Chen H; Department of Otolaryngology, Xiangya Hospital, Central South University, 87 Xiangya Road, Changsha, Hunan, China.
  • Cai X; Province Key Laboratory of Otolaryngology Critical Diseases, Changsha, Hunan, China.
  • Liu Y; Department of Otolaryngology, Xiangya Hospital, Central South University, 87 Xiangya Road, Changsha, Hunan, China.
  • Men M; Province Key Laboratory of Otolaryngology Critical Diseases, Changsha, Hunan, China.
  • Liu XZ; Department of Otolaryngology, Xiangya Hospital, Central South University, 87 Xiangya Road, Changsha, Hunan, China.
  • Yan D; Province Key Laboratory of Otolaryngology Critical Diseases, Changsha, Hunan, China.
  • Ling J; Department of Otolaryngology, Xiangya Hospital, Central South University, 87 Xiangya Road, Changsha, Hunan, China.
  • Feng Y; Province Key Laboratory of Otolaryngology Critical Diseases, Changsha, Hunan, China.
Neural Plast ; 2019: 7143458, 2019.
Article em En | MEDLINE | ID: mdl-30936914
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Fenótipo / Síndrome de Waardenburg / Polimorfismo de Nucleotídeo Único / Genótipo Tipo de estudo: Diagnostic_studies / Prognostic_studies Limite: Female / Humans / Male País/Região como assunto: Asia Idioma: En Revista: Neural Plast Assunto da revista: NEUROLOGIA Ano de publicação: 2019 Tipo de documento: Article País de afiliação: China
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Fenótipo / Síndrome de Waardenburg / Polimorfismo de Nucleotídeo Único / Genótipo Tipo de estudo: Diagnostic_studies / Prognostic_studies Limite: Female / Humans / Male País/Região como assunto: Asia Idioma: En Revista: Neural Plast Assunto da revista: NEUROLOGIA Ano de publicação: 2019 Tipo de documento: Article País de afiliação: China