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Article

Molecular characterization of Fanconi anaemia group C (FAC) gene polymorphisms.

Molecular and cellular probes - 1 Jun 1996

Savoia A, Centra M, Ianzano L, Pio de Cillis G, Buchwald M, Zelante L

Abstract excerpt

Fanconi anaemia (FA) is a genetically heterogeneous disease with defects in at least five genes. The gene for complementation group C (FAC) has been cloned and mapped to chromosome 9q22.3 in the interval between D9S280 and D9S287. Linkage analysis is a rapid tool for the exclusion of FA families from complementation group C. The currently available markers are informative microsatellites flanking FAC and an...

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Identifiers

PMID: 8799375
DOI: 10.1006/mcpr.1996.0029

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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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