Whole‐exome sequencing facilitates the differential diagnosis of <scp>Ehlers–Danlos</scp> syndrome ( <scp>EDS</scp> )-Reference-Cited by-同舟云学术

Whole‐exome sequencing facilitates the differential diagnosis of Ehlers–Danlos syndrome ( EDS )

Published:2022-02-04 Issue:3 Volume:10 Page:
ISSN:2324-9269
Container-title:Molecular Genetics & Genomic Medicine
language:en
Short-container-title:Molec Gen & Gen Med

Author:

Yang Fang¹²^ORCID,Yang Rong‐Juan³,Li Qian⁴,Zhang Jing⁵,Meng Yan‐Xin⁵,Liu Xiao‐Jun⁶,Yao Yong‐Feng¹²

Affiliation:

1. Department of Dermatology Shenzhen People's Hospital (The Second Clinical Medical College, Jinan University; The First Affiliated Hospital, Southern University of Science and Technology) Shenzhen China

2. Candidate Branch of National Clinical Research Center for Skin Diseases Shenzhen China

3. Department of Obstetrics Shijiazhuang Obstetrics and Gynecology Hospital Shijiazhuang China

4. National Research Institute for Family Planning Beijing China

5. Prenatal Diagnosis Center Shijiazhuang Obstetrics and Gynecology Hospital Shijiazhuang China

6. Department of Intensive Care Unit Shenzhen People's Hospital (The Second Clinical Medical College, Jinan University; The First Affiliated Hospital, Southern University of Science and Technology) Shenzhen China

Funder

National Key Research and Development Program of China

Publisher

Wiley

Subject

Genetics (clinical),Genetics,Molecular Biology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/mgg3.1885

Reference24 articles.

1. The Ehlers–Danlos syndromes

2. Vascular aspects of the Ehlers-Danlos Syndromes

3. The 2017 international classification of the Ehlers-Danlos syndromes

4. Characteristics, Diagnosis, and Management of Ehlers-Danlos Syndromes

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