An unexpected transmission of von Willebrand disease type 3: the first case of maternal uniparental disomy 12
Author:
Publisher
Ferrata Storti Foundation (Haematologica)
Subject
Hematology
Cited by 7 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. False positive non-invasive prenatal testing (NIPT) for trisomy 12 in a pregnancy associated with a favorable fetal outcome and normal hemogram in the pregnant woman;Taiwanese Journal of Obstetrics and Gynecology;2024-03
2. Primary Hemostasis Disorders as a Cause of Heavy Menstrual Bleeding in Women of Reproductive Age;Journal of Clinical Medicine;2023-09-01
3. Prenatal diagnosis of mosaicism for trisomy 12 in a single colony at amniocentesis in a pregnancy with a favorable outcome;Taiwanese Journal of Obstetrics and Gynecology;2020-07
4. Four children with postnatally diagnosed mosaic trisomy 12: Clinical features, literature review, and current diagnostic capabilities of genetic testing;American Journal of Medical Genetics Part A;2020-01-08
5. Segmental uniparental disomy as a rare cause of congenital severe factor XIII deficiency in a girl with only one heterozygous carrier parent;Pediatric Hematology and Oncology;2018-11-17
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