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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

Related topics

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5 relations
AnemiaBone MarrowFANCG geneFANCG protein, human

Papers overview

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2017
2017
Novel Founder Mutation in FANCA Gene (c.3446_3449dupCCCT) Among Romani Patients from the Balkan Region
Background: Fanconi anemia is a rare autosomal recessive or X-linked disorder characterised by clinical and genetic heterogeneity… 
2015
2015
Hematological consequences of a FANCG founder mutation in Black South African patients with Fanconi anemia.
2014
2014
Interleukin 8/KC enhances G-CSF induced hematopoietic stem/progenitor cell mobilization in Fancg deficient mice.
BACKGROUND Fanconi anemia (FA) is a heterogeneous genetic disorder characterized by a progressive bone marrow aplasia… 
2013
2013
Fanconi anaemia in black South African patients heterozygous for the FANCG c.637-643delTACCGCC founder mutation.
BACKGROUND Fanconi anaemia (FA) is an autosomal recessive, genetically heterogeneous disorder, characterised by interstrand… 
Review
2011
Review
2011
Fanconi anemia.
  • J. Soulier
  • Hematology. American Society of Hematology…
  • 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
Estudo das mutações do gene FANCG em pacientes com quadro clinico sugestivo de anemia de Fanconi
A Anemia de Fanconi (AF) e uma doenca caracterizada por multiplas anomalias congenitas, progressiva falha da medula ossea e alto… 
2005
2005
α II Spectrin Interacts with Specific Proteins in the Nucleus: Relevance to Fanconi Anemia.
Fanconi anemia (FA) is a genetic disorder characterized by bone marrow failure, a predisposition to cancer, congenital… 
2003
2003
Role of Fanconi Anemia FANCG in Preventing Double-Strand Breakage and Chromosomal Rearrangement during DNA Replication
The Fanconi anemia (FA) proteins overlap with those of homologous recombination through FANCD1/BRCA2, but the biochemical… 
Review
2002
Review
2002
Molecular biology of Fanconi anaemia—an old problem, a new insight
Fanconi anaemia (FA) comprises a group of autosomal recessive disorders resulting from mutations in one of eight genes (FANCA… 
2001
2001
[Chart 48: FANCG/XRCC9 (type G Fanconi's anemia)].
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