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15q26.1

A chromosome band present on 15q
National Institutes of Health

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10 relations
15qBLM wt AlleleCRTC3 wt AlleleChromosomes

Papers overview

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2014
2014
Characterization of a 520 kb deletion on chromosome 15q26.1 including ST8SIA2 in a patient with behavioral disturbance, autism spectrum disorder, and epilepsy
We present a patient with a behavioral disorder, epilepsy, and autism spectrum disorder who has a 520 kb chromosomal deletion at… 
2013
2013
Genome-wide linkage scan of quantitative traits representing symptom dimensions in multiplex schizophrenia families
2008
2008
Defective lamellar granule secretion in arthrogryposis, renal dysfunction, and cholestasis syndrome caused by a mutation in VPS33B.
BACKGROUND Arthrogryposis, renal dysfunction, and cholestasis (ARC) syndrome is a rare and usually fatal metabolic autosomal… 
2006
2006
Prenatal diagnosis of de novo deletions of 8p23.1 or 15q26.1 in two fetuses with diaphragmatic hernia and congenital heart defects
To show the importance of using high‐resolution chromosome analysis and FISH‐technique for finding subtle chromosomal lesions in… 
Review
2005
Review
2005
Terminal Deletion of Chromosome 15q26.1: Case Report and Brief Literature Review
Terminal deletions of chromosome 15q are rare events, with only six cases previously described. Here we describe a seventh case… 
Highly Cited
2001
Highly Cited
2001
Additional complexity on human chromosome 15q: identification of a set of newly recognized duplicons (LCR15) on 15q11-q13, 15q24, and 15q26.
Several cytogenetic alterations affect the distal part of the long arm of human chromosome 15, including recurrent rearrangements… 
Highly Cited
1995
Highly Cited
1995
Insulin-like growth factor I receptor expression and function in fibroblasts from two patients with deletion of the distal long arm of chromosome 15.
Most patients with deletion of the distal long arm of chromosome 15 have intrauterine growth retardation and postnatal growth… 
Highly Cited
1994
Highly Cited
1994
Linkage disequilibrium between the FES, D15S127, and BLM loci in Ashkenazi Jews with Bloom syndrome.
Bloom syndrome (BS) is more common in the Ashkenazi Jewish than in any other population. Approximately 1 in 110 Ashkenazi Jews… 
Highly Cited
1993
Highly Cited
1993
Assignment of the human aggrecan gene (AGC1) to 15q26 using fluorescence in situ hybridization analysis.
The large aggregating proteoglycan aggrecan is a major structural component of the extracellular matrix of articular cartilage… 
1984
1984
Localization of the cellular oncogenes ABL, SIS, and FES on human germ-line chromosomes.
The human germ-line positions of the oncogenes ABL, SIS, and FES, the cellular counterparts of the v-onc genes of Abelson murine… 
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