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Article

Severe factor X deficiency in a pair of siblings: clinical presentation, phenotypic and genotypic features, prenatal diagnosis and treatment.

Haemophilia : the official journal of the World Federation of Hemophilia - 1 May 2007

Ingerslev J, Herlin T, Sørensen B, Clausen N, Chu K C, High K A

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Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

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Identifiers

PMID: 17498086
DOI: 10.1111/j.1365-2516.2007.01466.x

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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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