The diagnosis of a haemophilia A carrier over 2 decades

Haemophilia. 2021 Jan;27(1):e133-e136. doi: 10.1111/hae.14073. Epub 2020 Jun 11.

Authors

Evemie Dubé¹, Julie Gauthier^{2

3}, Clémence Merlen¹, Arnaud Bonnefoy¹, Francoise Couture², David Lillicrap⁴, Georges-Etienne Rivard¹

Affiliations

¹ Division of Hematology-Oncology, Department of Pediatrics, CHU Sainte-Justine, Université de Montréal, Montreal, QC, Canada.
² Molecular Diagnostic Laboratory, CHU Sainte-Justine, Montreal, QC, Canada.
³ Department of Pediatrics, CHU Sainte-Justine, Université de Montréal, Montreal, QC, Canada.
⁴ Department of Medicine, Department of Pathology and Molecular Medicine, Queen's University, Kingston, ON, Canada.

PMID: 32526814
DOI: 10.1111/hae.14073

No abstract available

Publication types

Letter

MeSH terms

Factor VIII / genetics
Female
Genetic Carrier Screening
Hemophilia A* / diagnosis
Hemophilia A* / genetics
Heterozygote
Humans
Pregnancy
Prenatal Diagnosis

Substances

Factor VIII

Grants and funding

Bayer for Center of Excellence in Haemostasis