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Evidence for at least four Fanconi anaemia genes including FACC on chromosome 9

Data up to Jan 2025

Published1992
Citations305
References26
Clinical Trials (1)

Total Citations Per Year

Abstract

References (26)

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Spectrum of anomalies in Fanconi anaemia.

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Formal genetics of Fanconi's anemia

1976 • 195 citations

Genetic complementation analysis of ataxia telangiectasia and Nijmegen breakage syndrome: a survey of 50 patients

1988 • 188 citations

Identification of two complementation groups in Fanconi anemia

1985 • 159 citations

Hypomutability in Fanconi anemia cells is associated with increased deletion frequency at the HPRT locus.

1990 • 120 citations

Specific cellular defects in patients with Fanconi anemia

1979 • 118 citations

Xeroderma pigmentosum complementation group H falls into complementation group D

1991 • 80 citations

Expression of prokaryotic genes for hygromycin B and G418 resistance as dominant-selection markers in mouse L cells

1984 • 77 citations

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Fanconi anemia: Evidence for linkage heterogeneity on chromosome 20q

1991 • 48 citations

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1991 • 32 citations

Fluorescence-based viability assay for studies of reactive drug intermediates

1989 • 31 citations

Complementation and Gene Transfer Studies in Fanconi Anemia

1989 • 13 citations

Complementation studies between Fanconi's anemia cells with different DNA repair characteristics

1983 • 13 citations

Analysis of heterogeneity in Fanconi's anemia patients of different ethnic origin

1982 • 12 citations

Fanconi Anaemia: Clinical, Cytogenetic and Experimental Aspects

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Of Genes and Phenotypes

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Evidence for at least four Fanconi anaemia genes including FACC on chromosome 9 (1992) – Nature Genetics | Metascience Observatory Explorer