Inherited FANCD1/BRCA2 exon 7 splice mutations associated with acute myeloid leukaemia in Fanconi anaemia D1 are not found in sporadic childhood leukaemia
- 1 September 2005
- journal article
- Published by Wiley in British Journal of Haematology
- Vol. 130 (5) , 796-797
- https://doi.org/10.1111/j.1365-2141.2005.05677.x
Abstract
No abstract availableKeywords
This publication has 5 references indexed in Scilit:
- Biallelic BRCA2 mutations are associated with multiple malignancies in childhood including familial Wilms tumourJournal of Medical Genetics, 2005
- A cross‐linker‐sensitive myeloid leukemia cell line from a 2‐year‐old boy with severe Fanconi anemia and biallelic FANCD1/BRCA2 mutationsGenes, Chromosomes and Cancer, 2005
- Heterogeneity in Fanconi anemia: evidence for 2 new genetic subtypesBlood, 2004
- Cancer in Fanconi anemia, 1927–2001Cancer, 2003
- Biallelic Inactivation of BRCA2 in Fanconi AnemiaScience, 2002