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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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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… 
2005
2005
An analphoid marker chromosome inv dup(15)(q26.1qter), detected during prenatal diagnosis and characterized via chromosome microdissection
A small, mosaic, C-band negative marker chromosome was detected in amniocyte cultures during prenatal diagnosis due to advanced… 
2004
2004
Comments on “congenital Diaphragmatic Hernia: Is 15q26.1‐26.2 a candidate locus?”
In the Journal, Biggio et al. [2004] questioned if 15q26.1-26.2 is a candidate locus of congenital diaphragmatic hernia (CDH… 
1999
1999
Ashkenazi Jewish population frequency of the Bloom syndrome gene 2281 delta 6ins7 mutation.
Bloom syndrome is an autosomal recessive disorder characterized clinically by small size, sun-sensitive facial erythema, and… 
1998
1998
Partial trisomy 8q and partial monosomy 15q associated with congenital hydrocephalus, diaphragmatic hernia, uinary tract anomalies, congenital heart defect and kyphoscoliosis
We describe perinatal findings in a female fetus with partial trisomy 8q(8q24.1→8qter) and partial monosomy 15q(15q26.1→15qter… 
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… 
1993
1993
Confirmation of 15q26.1 as the site of the FES protooncogene by fluorescence in situ hybridization.
The FES oncogene was previously localized to human chromosome 15 by analysis of mouse x human somatic cell hybrids and to 15q26… 
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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