State of the art of genetic studies in hemophilia carriers
Author:
Publisher
Ovid Technologies (Wolters Kluwer Health)
Subject
Hematology,General Medicine
Reference8 articles.
1. Diagnosis of inherited bleeding disorders in the genomic era;Sivapalaratnam;Br J Haematol,2017
2. Prenatal and preimplantation genetic diagnosis;Vermeesch;Nat Rev,2016
3. Phenotype–genotype correlations in hemophilia A carriers are consistent with the binary role of the phase between F8 and X-chromosome inactivation;Radic;J Thromb Haemost,2015
4. Moderate X-chromosome inactivation skewing underlies factor VIII activity in symptomatic carriers from a family with mild haemophilia A;Cygan;Haemophilia,2016
5. Mosaicism in men in hemophilia: is it exceptional? Impact on genetic counselling;Costa;J Thromb Haemost,2009
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. Preoperative diagnosis and management of inherited bleeding disorders in female adolescents and adults;Canadian Journal of Surgery;2023-05-02
2. The effect of carriers’ reproductive choices and pregnancy history on sporadic severe haemophilia: A 20‐year retrospective study through a regional registry;Haemophilia;2022-01-20
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