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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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2013
2013
BACKGROUND Fanconi anaemia (FA) is an autosomal recessive, genetically heterogeneous disorder, characterised by interstrand… 
2013
2013
Fanconi anemia (FA) is a rare disorder characterized by physical abnormalities, bone marrow failure (BMF), increased risk of… 
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… 
2004
2004
Fanconi anemia (FA) is characterized by chromosomal instability and bone marrow hypoplasia. To explore the mechanism of FA… 
2003
2003
The Fanconi anemia (FA) proteins overlap with those of homologous recombination through FANCD1/BRCA2, but the biochemical… 
2002
2002
Taille et organisation du gene : 6 Kb, 14 exons, codant pour 2 ARN de 2,2 et 2,5 Kb (majoritaire). Taille de la proteine : 622…