Condition: fanconi anemia complementation group g


rs121434425 in FANCG gene and fanconi anemia complementation group g PMID 11093276 2000 Spectrum of mutations in the Fanconi anaemia group G gene, FANCG/XRCC9.

PMID 9806548 1998 The Fanconi anaemia group G gene FANCG is identical with XRCC9.

PMID 15657175 2005 A common Fanconi anemia mutation in black populations of sub-Saharan Africa.

PMID 24763404 2014 Targeted resequencing of 52 bone marrow failure genes in patients with aplastic anemia reveals an increased frequency of novel variants of unknown significance only in SLX4.

PMID 23613520 2013 Massively parallel sequencing, aCGH, and RNA-Seq technologies provide a comprehensive molecular diagnosis of Fanconi anemia.

PMID 12552564 2003 Spectrum of sequence variation in the FANCG gene: an International Fanconi Anemia Registry (IFAR) study.