𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Mutations in Fanconi anemia genes and the risk of esophageal cancer

✍ Scribed by Mohammad R. Akbari; Reza Malekzadeh; Pierre Lepage; David Roquis; Ali R. Sadjadi; Karim Aghcheli; Abbas Yazdanbod; Ramin Shakeri; Jafar Bashiri; Masoud Sotoudeh; Akram Pourshams; Parviz Ghadirian; Steven A. Narod

Publisher
Springer
Year
2011
Tongue
English
Weight
228 KB
Volume
129
Category
Article
ISSN
0340-6717

No coin nor oath required. For personal study only.

πŸ“œ SIMILAR VOLUMES

Novel mutations and polymorphisms in the
Novel mutations and polymorphisms in the Fanconi anemia group C gene
✍ Rachel A. Gibson; Neil V. Morgan; Laura H. Goldstein; Ian C. Pearson; Ian P. Kes πŸ“‚ Article πŸ“… 1996 πŸ› John Wiley and Sons 🌐 English βš– 982 KB

## Ponder Fanconi anemia (FA) is an autosomal recessive disorder associated with hypersensitivity to DNA cross-linking agents and bone marrow failure. At least four complementation groups have been defined, and the FA group C gene (FAC) has been cloned. We have screened 76 unrelated FA patients of

Identification and characterization of n
Identification and characterization of novel mutations of the major Fanconi anemia gene FANCA in the Japanese population
✍ Hiroshi Yagasaki; Satoshi Hamanoue; Tsukasa Oda; Tatsutoshi Nakahata; Shigetaka πŸ“‚ Article πŸ“… 2004 πŸ› John Wiley and Sons 🌐 English βš– 324 KB πŸ‘ 2 views

Fanconi anemia (FA) is a rare autosomal recessive disorder of hematopoiesis, with at least 11 complementation groups. FANCA, a gene for group A, accounts for the majority of FA patients. Previous studies of FANCA mutations revealed high allelic heterogeneity, frequent occurrence of large deletions,