Copy number variation characterization and possible candidate genes in miscarriage and stillbirth by next‐generation sequencing analysis-Reference-Cited by-同舟云学术

Copy number variation characterization and possible candidate genes in miscarriage and stillbirth by next‐generation sequencing analysis

Published:2021-08-20 Issue:12 Volume:23 Page:
ISSN:1099-498X
Container-title:The Journal of Gene Medicine
language:en
Short-container-title:J Gene Med

Author:

Zhang Xia¹²,Huang Qingyan²³,Yu Zhikang²³,Wu Heming²³^ORCID

Affiliation:

1. Center for Prenatal Disgnosis, Meizhou People's Hospital (Huangtang Hospital) Meizhou Academy of Medical Sciences Meizhou China

2. Guangdong Provincial Key Laboratory of Precision Medicine and Clinical Translational Research of Hakka Population, Meizhou People's Hospital (Huangtang Hospital) Meizhou Academy of Medical Sciences Meizhou China

3. Center for Precision Medicine, Meizhou People's Hospital (Huangtang Hospital) Meizhou Academy of Medical Sciences Meizhou China

Publisher

Wiley

Subject

Genetics (clinical),Drug Discovery,Genetics,Molecular Biology,Molecular Medicine

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/jgm.3383

Reference61 articles.

1. Circulating levels of inhibin A, activin A and follistatin in missed and recurrent miscarriages

2. Parents’ experiences of care following the loss of a baby at the margins between miscarriage, stillbirth and neonatal death: a UK qualitative study

3. Miscarriage matters: the epidemiological, physical, psychological, and economic costs of early pregnancy loss

4. Genetic innovations and our understanding of stillbirth

5. Chromosomal karyotype in chorionic villi of recurrent spontaneous abortion patients

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4. Analysis of copy number variations and possible candidate genes in spontaneous abortion by copy number variation sequencing;Frontiers in Endocrinology;2023-10-17

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