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Article

Validation of Fanconi anemia complementation Group A assignment using molecular analysis.

Genetics in medicine : official journal of the American College of Medical Genetics - 1 Mar 2009

Moghrabi Nabil N, Johnson Monique A, Yoshitomi Marvin J, Zhu Xiaoman, Al-Dhalimy Muhsen J, Olson Susan B, Grompe Markus, Richards C Sue

Abstract excerpt

PURPOSE: Fanconi anemia is a genetically heterogeneous chromosomal breakage disorder exhibiting a high degree of clinical variability. Clinical diagnoses are confirmed by testing patient cells for increased sensitivity to crosslinking agents. Fanconi anemia complementation group assignment, essen...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 19367192
DOI: 10.1097/GIM.0b013e318193ba67

Genes

FANCA
FANCC

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-19367192-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

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