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UnknownComplementation analysis in Fanconi anemia: assignment of the reference FA-H patient to group A.
Not available
S-EPMC1287536 | biostudies-literature
UnknownHigh frequency of large intragenic deletions in the Fanconi anemia group A gene.
Not available
S-EPMC1288285 | biostudies-literature
UnknownAnalysis of baseline and cisplatin-inducible gene expression in Fanconi anemia cells using oligonucleotide-based microarrays.
Not available
S-EPMC138804 | biostudies-literature
UnknownDiagnosis of Fanconi Anemia: Mutation Analysis by Multiplex Ligation-Dependent Probe Amplification and PCR-Based Sanger Sequencing.
Not available
S-EPMC3388349 | biostudies-literature
UnknownA "late-but-fitter revertant cell" explains the high frequency of revertant mosaicism in epidermolysis bullosa.
Not available
S-EPMC5823395 | biostudies-literature
UnknownCoregulation of FANCA and BRCA1 in human cells.
Not available
S-EPMC4143540 | biostudies-literature
UnknownWarsaw breakage syndrome, a cohesinopathy associated with mutations in the XPD helicase family member DDX11/ChlR1.
Not available
S-EPMC2820174 | biostudies-literature
UnknownA strategy for molecular diagnostics of Fanconi anemia in Brazilian patients.
Not available
S-EPMC5511800 | biostudies-literature
UnknownMolecular and genealogical evidence for a founder effect in Fanconi anemia families of the Afrikaner population of South Africa.
Not available
S-EPMC33282 | biostudies-literature
UnknownA human ortholog of archaeal DNA repair protein Hef is defective in Fanconi anemia complementation group M.
Not available
S-EPMC2704909 | biostudies-literature
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