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Segmental uniparental disomy as a rare cause of congenital severe factor XIII deficiency in a girl with only one heterozygous carrier parent

  • Published:2018-11-17 Issue:7-8 Volume:35 Page:442-446
  • ISSN:0888-0018
  • Container-title:Pediatric Hematology and Oncology
  • language:en
  • Short-container-title:Pediatric Hematology and Oncology

Author:

Shen Ming-Ching123ORCID,Chen Ming4,Chang Shung-Ping4,Lin Po-Te2,Hsieh Han-Ni2,Lin Kai-Hsin5

Affiliation:

1. Department of Laboratory Medicine, National Taiwan University Hospital, Taipei, Taiwan;

2. Department of Internal Medicine, Changhua Christian Hospital, Changhua, Taiwan;

3. Department of Laboratory Medicine, Changhua Christian Hospital, Changhua, Taiwan;

4. Department of Genomic Medicine, Changhua Christian Hospital, Changhua, Taiwan;

5. Department of Pediatrics, National Taiwan University Hospital, Taipei, Taiwan

Publisher

Informa UK Limited

Subject

Oncology,Hematology,Pediatrics, Perinatology, and Child Health

Cited by 2 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Novel Insights into Heterozygous Factor XIII Deficiency;Seminars in Thrombosis and Hemostasis;2023-03-20

2. Congenital Factor XIII Deficiency, Diagnosis, and Management;Congenital Bleeding Disorders;2023
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