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9q22.3

A chromosome band present on 9q
National Institutes of Health

Related topics

Related topics

4 relations
ChromosomesFANCC wt AllelePTCH1 wt AlleleXPA wt Allele

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
Review
2015
Review
2015
Basal cell nevus syndrome or Gorlin syndrome.
2010
2010
Genetic inactivation of the Fanconi anemia gene FANCC identified in the hepatocellular carcinoma cell line HuH-7 confers sensitivity towards DNA-interstrand crosslinking agents
BackgroundInactivation of the Fanconi anemia (FA) pathway through defects in one of 13 FA genes occurs at low frequency in… 
Highly Cited
2008
Highly Cited
2008
Alterations in candidate genes PHF2, FANCC, PTCH1 and XPA at chromosomal 9q22.3 region: Pathological significance in early- and late-onset breast carcinoma
IntroductionYounger women with breast carcinoma (BC) exhibits more aggressive pathologic features compared to older women; young… 
Highly Cited
2006
Highly Cited
2006
Interstitial 9q22.3 microdeletion: clinical and molecular characterisation of a newly recognised overgrowth syndrome
In the course of a systematic whole genome screening of patients with unexplained overgrowth syndrome by microarray-based… 
Highly Cited
2005
Highly Cited
2005
High‐resolution detection and mapping of genomic DNA alterations in neuroblastoma
We used array‐based comparative genomic hybridization (aCGH) to measure genomic copy number alterations (CNAs) in 42… 
Highly Cited
2000
Highly Cited
2000
Sporadic trichoepithelioma demonstrates deletions at 9q22.3.
BACKGROUND Trichoepithelioma (TE) is a benign cutaneous tumor that originates from hair follicles and occurs either in multiple… 
Highly Cited
1999
Highly Cited
1999
Four tumor suppressor loci on chromosome 9q in bladder cancer: evidence for two novel candidate regions at 9q22.3 and 9q31
The most common genetic alteration identified in transitional cell carcinoma (TCC) of the bladder is loss of heterozygosity (LOH… 
Highly Cited
1997
Highly Cited
1997
Most germ-line mutations in the nevoid basal cell carcinoma syndrome lead to a premature termination of the PATCHED protein, and no genotype-phenotype correlations are evident.
The human homologue of the Drosophila segment polarity gene patched is implicated in the development of nevoid basal cell… 
Highly Cited
1996
Highly Cited
1996
Erratum: Expression cloning of a cDNA for the major Fanconi anaemia gene, FAA
J R L T Foe, M A Rooimans, L Bosnoyan-Collins, N Alon, M Wijker, L Parker, J Lightfoot, M Carreau, D F Callen, A Savoia, N C… 
Highly Cited
1992
Highly Cited
1992
Evidence for at least four Fanconi anaemia genes including FACC on chromosome 9
Fanconi anaemia (FA) is a DNA repair disorder characterized by cellular hypersensitivity to DNA cross–linking agents and… 
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