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fanconi anemia complementation group g

Known as: FANCG, FANCONI ANEMIA, COMPLEMENTATION GROUP G 
Fanconi anemia caused by mutations of the FANCG gene.
National Institutes of Health

Papers overview

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2017
2017
Background: Fanconi anemia is a rare autosomal recessive or X-linked disorder characterised by clinical and genetic heterogeneity… 
2014
2014
BACKGROUND Fanconi anemia (FA) is a heterogeneous genetic disorder characterized by a progressive bone marrow aplasia… 
2013
2013
BACKGROUND Fanconi anaemia (FA) is an autosomal recessive, genetically heterogeneous disorder, characterised by interstrand… 
Review
2011
Review
2011
  • J. Soulier
  • 2011
  • Corpus ID: 265716813
Fanconi anemia (FA) is the most frequent inherited cause of BM failure (BMF). Fifteen FANC genes have been identified to date… 
2006
2006
A Anemia de Fanconi (AF) e uma doenca caracterizada por multiplas anomalias congenitas, progressiva falha da medula ossea e alto… 
2005
2005
Fanconi anemia (FA) is a genetic disorder characterized by bone marrow failure, a predisposition to cancer, congenital… 
2003
2003
The Fanconi anemia (FA) proteins overlap with those of homologous recombination through FANCD1/BRCA2, but the biochemical… 
Review
2002
Review
2002
Fanconi anaemia (FA) comprises a group of autosomal recessive disorders resulting from mutations in one of eight genes (FANCA…