Clinical phenotypes study of 231 children with Williams syndrome in China: A single‐center retrospective study-Reference-Cited by-同舟云学术

Clinical phenotypes study of 231 children with Williams syndrome in China: A single‐center retrospective study

Published:2022-09-27 Issue:12 Volume:10 Page:
ISSN:2324-9269
Container-title:Molecular Genetics & Genomic Medicine
language:en
Short-container-title:Molec Gen & Gen Med

Author:

Li Fang‐fang¹^ORCID,Chen Wei‐jun¹,Yao Dan¹,Xu Lin¹,Shen Ji‐yang¹,Zeng Yan¹,Shi Zhuo²,Ye Xiao‐wei³,Kang Dao‐huan⁴,Xu Bin⁵,Shao Jie¹,Ji Chai¹

Affiliation:

1. Department of Child Health Care, The Children's Hospital Zhejiang University School of Medicine, National Clinical Research Center for Child Health Hangzhou China

2. Department of Pediatric Cardio‐Thoracic Surgery, The Children's Hospital Zhejiang University School of Medicine, National Clinical Research Center for Child Health Hangzhou China

3. Department of Stomatology, The Children's Hospital Zhejiang University School of Medicine, National Clinical Research Center for Child Health Hangzhou China

4. Department of Ophthalmology, The Children's Hospital Zhejiang University School of Medicine, National Clinical Research Center for Child Health Hangzhou China

5. Department of Otorhinolaryngology‐head and Neck Surgery, The Children's Hospital Zhejiang University School of Medicine, National Clinical Research Center for Child Health Hangzhou China

Funder

Medical Science and Technology Project of Zhejiang Province

Natural Science Foundation of Zhejiang Province

Publisher

Wiley

Subject

Genetics (clinical),Genetics,Molecular Biology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/mgg3.2069

Reference39 articles.

1. BAZ1B is a candidate gene responsible for hypothyroidism in Williams syndrome

2. The epidemiological aspects of congenital heart disease in central and southern district of Iran