Your browser doesn't support javascript.
loading
Description of the molecular and phenotypic spectrum of Wiedemann-Steiner syndrome in Chinese patients.
Li, Niu; Wang, Yirou; Yang, Yu; Wang, Pengpeng; Huang, Hui; Xiong, Shiyi; Sun, Luming; Cheng, Min; Song, Cui; Cheng, Xinran; Ding, Yu; Chang, Guoying; Chen, Yao; Xu, Yufei; Yu, Tingting; Yao, Ru-En; Shen, Yiping; Wang, Xiumin; Wang, Jian.
Affiliation
  • Li N; Department of Medical Genetics and Molecular Diagnostic Laboratory, Shanghai Children's Medical Center, Shanghai Jiaotong University School of Medicine, Shanghai, 200127, China.
  • Wang Y; Institute of Pediatric Translational Medicine, Shanghai Children's Medical Center, Shanghai Jiao Tong University School of Medicine, Shanghai, 200127, China.
  • Yang Y; Department of Endocrinology and Metabolism, Shanghai Children's Medical Center, Shanghai Jiaotong University School of Medicine, Shanghai, 200127, China.
  • Wang P; Department of Endocrinology, Metabolism, and Genetics, Jiangxi Provincial Children's Hospital, Nanchang, 330029, Jiangxi, China.
  • Huang H; MyGenostics Inc., Beijing, 101318, China.
  • Xiong S; Central laboratory, Jiangxi Provincial Children's Hospital, Nanchang, 330029, Jiangxi, China.
  • Sun L; Fetal Medicine Unit & Prenatal diagnosis center, Shanghai First Maternity and Infant hospital, Tongji University School of Medicine, Shanghai, People's Republic of China.
  • Cheng M; Fetal Medicine Unit & Prenatal diagnosis center, Shanghai First Maternity and Infant hospital, Tongji University School of Medicine, Shanghai, People's Republic of China.
  • Song C; Department of Neurology, Children's Hospital of Chongqing Medical University, Chongqing, 400014, China.
  • Cheng X; Department of Endocrinology and Genetic Metabolic Diseases, Ministry of Education Key Laboratory of Child Development and Disorders, China International Science and Technology Cooperation Base of Child Development and Critical Disorders. Chongqing Key Laboratory of Pediatrics, Children's Hospital of
  • Ding Y; Department of Endocrinology and Metabolism, Chengdu Women's and Children's Central Hospital, Sichuan Province, Chengdu, 610091, China.
  • Chang G; Department of Endocrinology and Metabolism, Shanghai Children's Medical Center, Shanghai Jiaotong University School of Medicine, Shanghai, 200127, China.
  • Chen Y; Department of Endocrinology and Metabolism, Shanghai Children's Medical Center, Shanghai Jiaotong University School of Medicine, Shanghai, 200127, China.
  • Xu Y; Department of Endocrinology and Metabolism, Shanghai Children's Medical Center, Shanghai Jiaotong University School of Medicine, Shanghai, 200127, China.
  • Yu T; Department of Medical Genetics and Molecular Diagnostic Laboratory, Shanghai Children's Medical Center, Shanghai Jiaotong University School of Medicine, Shanghai, 200127, China.
  • Yao RE; Department of Medical Genetics and Molecular Diagnostic Laboratory, Shanghai Children's Medical Center, Shanghai Jiaotong University School of Medicine, Shanghai, 200127, China.
  • Shen Y; Institute of Pediatric Translational Medicine, Shanghai Children's Medical Center, Shanghai Jiao Tong University School of Medicine, Shanghai, 200127, China.
  • Wang X; Department of Medical Genetics and Molecular Diagnostic Laboratory, Shanghai Children's Medical Center, Shanghai Jiaotong University School of Medicine, Shanghai, 200127, China.
  • Wang J; Institute of Pediatric Translational Medicine, Shanghai Children's Medical Center, Shanghai Jiao Tong University School of Medicine, Shanghai, 200127, China.
Orphanet J Rare Dis ; 13(1): 178, 2018 10 11.
Article in En | MEDLINE | ID: mdl-30305169
Subject(s)
Key words
Fulltext
Add to My VHL
Print
XML
PubMed Links
Search on Google

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Abnormalities, Multiple / Histone-Lysine N-Methyltransferase / Myeloid-Lymphoid Leukemia Protein Limits: Adolescent / Adult / Child / Child, preschool / Humans / Infant / Male Country/Region as subject: Asia Language: En Journal: Orphanet J Rare Dis Journal subject: MEDICINA Year: 2018 Document type: Article Affiliation country: China Country of publication: Reino Unido
Fulltext
Add to My VHL
Print
XML
PubMed Links
Search on Google

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Abnormalities, Multiple / Histone-Lysine N-Methyltransferase / Myeloid-Lymphoid Leukemia Protein Limits: Adolescent / Adult / Child / Child, preschool / Humans / Infant / Male Country/Region as subject: Asia Language: En Journal: Orphanet J Rare Dis Journal subject: MEDICINA Year: 2018 Document type: Article Affiliation country: China Country of publication: Reino Unido