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Biallelic mutations of TTC12 and TTC21B were identified in Chinese patients with multisystem ciliopathy syndromes.
Chen, Weicheng; Wang, Feifei; Zeng, Weijia; Zhang, Xinyan; Shen, Libing; Zhang, Yuan; Zhou, Xiangyu.
Afiliação
  • Chen W; Obstetrics and Gynecology Hospital of Fudan University, Pediatric Cardiovascular Center at Children's Hospital of Fudan University, Fudan University Shanghai Medical College, Shanghai, 200011, China.
  • Wang F; Obstetrics and Gynecology Hospital of Fudan University, Pediatric Cardiovascular Center at Children's Hospital of Fudan University, Fudan University Shanghai Medical College, Shanghai, 200011, China.
  • Zeng W; State Key Lab of Genetic Engineering, School of Life Sciences, Fudan University, Shanghai, 200438, China.
  • Zhang X; Obstetrics and Gynecology Hospital of Fudan University, Pediatric Cardiovascular Center at Children's Hospital of Fudan University, Fudan University Shanghai Medical College, Shanghai, 200011, China.
  • Shen L; International Human Phenome Institutes (IHPI), Shanghai, 200433, China.
  • Zhang Y; Department of Assisted Reproduction, Shanghai First Maternity and Infant Hospital, Tongji University School of Medicine, Shanghai, 201204, China. yzhang150515@163.com.
  • Zhou X; , Shanghai, China. yzhang150515@163.com.
Hum Genomics ; 16(1): 48, 2022 10 22.
Article em En | MEDLINE | ID: mdl-36273201

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Prognostic_studies Limite: Animals / Humans / Newborn País/Região como assunto: Asia Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Prognostic_studies Limite: Animals / Humans / Newborn País/Região como assunto: Asia Idioma: En Ano de publicação: 2022 Tipo de documento: Article