Mutation analysis in the F8 gene in 485 families with haemophilia A and prenatal diagnosis in China-Reference-Cited by-同舟云学术

Mutation analysis in the F8 gene in 485 families with haemophilia A and prenatal diagnosis in China

Published:2020-11-27 Issue:1 Volume:27 Page:
ISSN:1351-8216
Container-title:Haemophilia
language:en
Short-container-title:Haemophilia

Author:

Feng Yin¹^ORCID,Li Qianqian¹,Shi Panlai¹,Liu Ning¹,Kong Xiangdong¹,Guo Ruixia²

Affiliation:

1. The Department of Obstetrics and Gynecology The Genetics and Prenatal Diagnosis Center The First Affiliated Hospital of Zhengzhou University Henan China

2. The Department of Obstetrics and Gynecology The First Affiliated Hospital of Zhengzhou University Henan China

Publisher

Wiley

Subject

Genetics (clinical),Hematology,General Medicine

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/hae.14206

Reference24 articles.

1. Haemophilia A and haemophilia B: molecular insights

2. Haemophilias A and B

3. The molecular analysis of haemophilia A: a guideline from the UK haemophilia centre doctors' organization haemophilia genetics laboratory network

4. Characterization of the human factor VIII gene

5. Nonhomologous recombination in the human genome: Deletions in the human factor VIII gene

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