Skip to search formSkip to main content
You are currently offline. Some features of the site may not work correctly.

15q15.3

A chromosome band present on 15q
National Institutes of Health

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2018
2018
Keloids are benign dermal tumors occurring approximately 20 times more often in individuals of African descent as compared to… Expand
  • table 2
Is this relevant?
2014
2014
OBJECTIVE Tumour biomarkers are used as indicators for cancer screening and as predictors for therapeutic responses and prognoses… Expand
  • figure 1
  • figure 2
  • figure 3
Is this relevant?
2014
2014
We present the case of two brothers who were referred to a male infertility clinic for infertility workup. Conventional… Expand
  • table 1
  • figure 1
Is this relevant?
2013
2013
BackgroundHearing loss is the most common birth defect and the most prevalent sensorineural disorder in developed countries. More… Expand
  • figure 1
  • figure 2
  • table 1
Is this relevant?
2009
2009
Syndromic hearing loss that results from contiguous gene deletions is uncommon.Three families with a novel syndrome characterised… Expand
Is this relevant?
2007
2007
BACKGROUND Syndromic hearing loss that results from contiguous gene deletions is uncommon. Deafness-infertility syndrome (DIS) is… Expand
Is this relevant?
2003
2003
Deletions found in several types of human tumor, including carcinomas of the colorectum, breast, and lung, suggest the presence… Expand
Is this relevant?
2001
2001
Autosomal dominant renal Fanconi syndrome is a genetic model for the study of proximal renal tubular transport pathology. We were… Expand
  • figure 1
  • table 1
  • figure 2
Is this relevant?
Highly Cited
2000
Highly Cited
2000
Two cDNAs encoding NADPH oxidases and constituting the thyroid H(2)O(2) generating system have been cloned. The strategy of… Expand
Is this relevant?
1995
1995
A gene for the recessive limb girdle muscular dystrophy LGMD2A (MIM 253600) was mapped within a 7-cM interval along Chromosome… Expand
  • table 1
  • figure 1
Is this relevant?