Trio‐whole‐exome sequencing and preimplantation genetic diagnosis for unexplained recurrent fetal malformations-Reference-Cited by-同舟云学术

Trio‐whole‐exome sequencing and preimplantation genetic diagnosis for unexplained recurrent fetal malformations

Published:2019-11-11 Issue:2 Volume:41 Page:432-448
ISSN:1059-7794
Container-title:Human Mutation
language:en
Short-container-title:Human Mutation

Author:

Guo Wei¹²³,Lai Yuchen¹²³⁴,Yan Zhiqiang¹²³⁴,Wang Yuqian¹²³,Nie Yanli¹²³,Guan Shuo¹²³,Kuo Ying¹²³,Zhang Wenxin¹²³,Zhu Xiaohui¹²³,Peng Mei⁵,Zhi Xu¹²³,Wei Yuan¹²³,Yan Liying¹²³^ORCID,Qiao Jie¹²³⁴⁶

Affiliation:

1. Department of Obstetrics and Gynecology, Center for Reproductive MedicinePeking University Third HospitalBeijing China

2. Key Laboratory of Assisted ReproductionMinistry of EducationBeijing China

3. Beijing Key Laboratory of Reproductive Endocrinology and Assisted ReproductionBeijing China

4. Peking‐Tsinghua Center for Life SciencesPeking UniversityBeijing China

5. iGenomix China China

6. Beijing Advanced Innovation Center for Genomics (ICG)Peking UniversityBeijing China

Funder

National Natural Science Foundation of China

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/humu.23935

Reference39 articles.

1. A null variant in PUS3 confirms its involvement in intellectual disability and further delineates the associated neurodevelopmental disease

2. Genetic spectrum of Saudi Arabian patients with antenatal cystic kidney disease and ciliopathy phenotypes using a targeted renal gene panel

3. The Centers for Mendelian Genomics: A new large-scale initiative to identify the genes underlying rare Mendelian conditions

4. Biallelic SZT2 Mutations Cause Infantile Encephalopathy with Epilepsy and Dysmorphic Corpus Callosum

5. Centrosomes and cilia in human disease

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