More Than Half the Sporadic Cases of Hemophilia A in Sweden Are Due to a Recent Mutation
Author:
Publisher
Wiley
Subject
General Medicine,Pediatrics, Perinatology and Child Health
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1651-2227.1991.tb11860.x/fullpdf
Reference22 articles.
1. Haemophilia in Sweden
2. THE SPORADIC CASE OF HÆMOPHILIA A
3. The Detection of Carriers of Classic Hemophilia: H. P. Smith Memorial Lecture
4. Carrier Studies in “Simplex Families”
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1. Origin of pathogenic variant and mosaicism in families with a sporadic case of haemophilia B;Haemophilia;2024-04-17
2. Prominent Mutation of Intron 22 Inversion in Sporadic Hemophilia: Is It Worth the Antenatal Screening?;The Application of Clinical Genetics;2022-05
3. Novel F8 and F9 gene variants from the PedNet hemophilia registry classified according to ACMG/AMP guidelines;Human Mutation;2020-10-14
4. Genotyping of Intron Inversions and Point Mutations in Exon 14 of the FVIII Gene in Iranian Azeri Turkish Families with Hemophilia A;Indian Journal of Hematology and Blood Transfusion;2016-06-27
5. Inversions of the factor VIII gene in Swedish patients with severe haemophilia A;European Journal of Haematology;2009-04-24
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