Polydactyly Patient Carried a Mutation of <i>PTCH1</i> Which Has Been Identified in Nevoid Basal Cell Nevus Syndrome.

Cao, Ruixue; Liu, Sijie; Chai, Weiran; Shen, Pinquan

Polydactyly Patient Carried a Mutation of PTCH1 Which Has Been Identified in Nevoid Basal Cell Nevus Syndrome.

Cao, Ruixue; Liu, Sijie; Chai, Weiran; Shen, Pinquan.

Afiliação

Cao R; Department of Pediatrics, The Second Affiliated Hospital and Yuying Children's Hospital of Wenzhou Medical University, Wenzhou, P.R. China.
Liu S; Department of Pediatric Cardiology, Xinhua Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, P.R. China.
Chai W; Department of Assisted Reproduction, Shanghai Ninth People's Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, P.R. China.
Shen P; Department of Pediatric Orthopedics, Xinhua Hospital Affiliated to Shanghai Jiaotong University School of Medicine, Shanghai, P.R. China.

DNA Cell Biol ; 39(10): 1754-1759, 2020 Oct.

Article em En | MEDLINE | ID: mdl-32716646

Assuntos

Mutação de Sentido Incorreto; Receptor Patched-1/genética; Polidactilia/genética; Pré-Escolar; Feminino; Humanos; Lactente; Masculino; Polidactilia/patologia; Irmãos

Palavras-chave

PTCH1; gene mutation; nevoid basal cell nevus syndrome; polydactyly

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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Polidactilia / Mutação de Sentido Incorreto / Receptor Patched-1 Tipo de estudo: Prognostic_studies Limite: Child, preschool / Female / Humans / Infant / Male Idioma: En Revista: DNA Cell Biol Assunto da revista: BIOLOGIA MOLECULAR Ano de publicação: 2020 Tipo de documento: Article País de publicação: Estados Unidos

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