Localization of the Fanconi Anemia Complementation Group D Gene to a 200-kb Region on Chromosome 3p25.3
- 1 May 2000
- journal article
- Published by Elsevier BV in American Journal of Human Genetics
- Vol. 66 (5), 1540-1551
- https://doi.org/10.1086/302896
Abstract
No abstract availableKeywords
This publication has 49 references indexed in Scilit:
- Expression cloning of a cDNA for the major Fanconi anaemia gene, FAANature Genetics, 1996
- Precise localisation of 3p25 breakpoints in four patients with the 3p-syndrome.Journal of Medical Genetics, 1996
- Enhanced expression of common fragile site with occupational exposure to pesticidesCancer Genetics and Cytogenetics, 1995
- Molecular genetic analysis of the 3p — syndromeHuman Molecular Genetics, 1994
- BR140, a Novel Zinc-Finger Protein with Homology to the TAF250 Subunit of TFIIDBiochemical and Biophysical Research Communications, 1994
- Hypersensitivity to oxygen is a uniform and secondary defect in Fanconi anemia cellsMutation Research/DNA Repair, 1993
- Basic local alignment search toolJournal of Molecular Biology, 1990
- Specific cellular defects in patients with Fanconi anemiaJournal of Cellular Physiology, 1979
- Phytohemagglutinin enhancement of cell fusion reduces polyethylene glycol cytotoxicityExperimental Cell Research, 1979
- Detection of specific sequences among DNA fragments separated by gel electrophoresisJournal of Molecular Biology, 1975