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Article

Carrier detection and prenatal diagnosis of hemophilia in developing countries.

Seminars in thrombosis and hemostasis - 1 Nov 2005

Peyvandi Flora

Abstract excerpt

Hemophilia A and B, inherited as X-linked recessive traits, are the most common hereditary hemorrhagic disorders caused by a deficiency or dysfunction of coagulation factor VIII (FVIII) or FIX, respectively. Hemophilia is prevalent worldwide, without ethnic or geographic limitations, and remains a life-threatening and often disabling condition. Advances in molecular medicine in this century have markedly improved...

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Identifiers

PMID: 16276463
DOI: 10.1055/s-2005-922226

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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