Detalhe da pesquisa
1.
Fanconi anemia is associated with a defect in the BRCA2 partner PALB2.
Nat Genet
; 39(2): 159-61, 2007 Feb.
Artigo
Inglês
| MEDLINE | ID: mdl-17200672
2.
The DNA helicase BRIP1 is defective in Fanconi anemia complementation group J.
Nat Genet
; 37(9): 934-5, 2005 Sep.
Artigo
Inglês
| MEDLINE | ID: mdl-16116423
3.
Effective CRISPR/Cas9-mediated correction of a Fanconi anemia defect by error-prone end joining or templated repair.
Sci Rep
; 9(1): 768, 2019 01 25.
Artigo
Inglês
| MEDLINE | ID: mdl-30683899
4.
Genetic subtyping of Fanconi anemia by comprehensive mutation screening.
Hum Mutat
; 29(1): 159-66, 2008 Jan.
Artigo
Inglês
| MEDLINE | ID: mdl-17924555
5.
Somatic genomic alterations in retinoblastoma beyond RB1 are rare and limited to copy number changes.
Sci Rep
; 6: 25264, 2016 04 29.
Artigo
Inglês
| MEDLINE | ID: mdl-27126562
6.
Multiple TPR motifs characterize the Fanconi anemia FANCG protein.
DNA Repair (Amst)
; 3(1): 77-84, 2004 Jan 05.
Artigo
Inglês
| MEDLINE | ID: mdl-14697762
7.
A Dutch Fanconi Anemia FANCC Founder Mutation in Canadian Manitoba Mennonites.
Anemia
; 2012: 865170, 2012.
Artigo
Inglês
| MEDLINE | ID: mdl-22701786
8.
Evidence for complete epistasis of null mutations in murine Fanconi anemia genes Fanca and Fancg.
DNA Repair (Amst)
; 10(12): 1252-61, 2011 Dec 10.
Artigo
Inglês
| MEDLINE | ID: mdl-22036606
9.
Characterization, expression and complex formation of the murine Fanconi anaemia gene product Fancg.
Genes Cells
; 7(3): 333-42, 2002 Mar.
Artigo
Inglês
| MEDLINE | ID: mdl-11918676