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12q15

A chromosome band present on 12q
National Institutes of Health

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12qChromosomesFRS2 wt AlleleHMGA2 wt Allele

Papers overview

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2019
2019
A heterozygous, intragenic deletion of CNOT2 recapitulates the phenotype of 12q15 deletion syndrome
Only a few individuals with 12q15 deletion have been described, presenting with a disorder characterized by learning disability… 
2010
2010
Screening for DNA copy number aberrations in mucinous adenocarcinoma arising from the minor salivary gland: two case reports.
2007
2007
A clonal t(8;12)(p11.2;q24.3) as the sole abnormality in a solitary fibrous tumor of the pleura.
2006
2006
Identification and characterization of novel human transcripts embedded within HMGA2 in t(12;14)(q15;q24.1) uterine leiomyoma.
1998
1998
The t(3;12)(q27;q14‐q15) with underlying HMGIC‐LPP fusion is not determining an adipocytic phenotype
The HMGIC gene, located in chromosome band 12q15, is rearranged in many different benign human tumors, often resulting in its… 
Highly Cited
1996
Highly Cited
1996
Gains and losses of DNA sequences in liposarcomas evaluated by comparative genomic hybridization
Comparative genomic hybridization (CGH) was used to detect and map the regions of gain, high‐level amplification, and loss of DNA… 
1996
1996
The t(1; 12)(p36;q13) in a Renal Oncocytoma
A new chromosome rearrangement, t(1;12)(p36;q13). is added to the cytogenetic changes found in renal oncocytomas. The breakpoint… 
1995
1995
A 6-Mb yeast artificial chromosome contig and long-range physical map encompassing the region on chromosome 12q15 frequently rearranged in a variety of benign solid tumors.
Cytogenetic analysis of a variety of benign solid tumors, among which uterine leiomyoma, lipoma, pleomorphic salivary gland… 
1995
1995
Regional fine mapping of the multiple‐aberration region involved in uterine leiomyoma, lipoma, and pleomorphic adenoma of the salivary gland to 12q15
Cytogenetic aberrations involving 12q13‐15 are frequently observed in a variety of benign solid tumors. Using a chromosome… 
1990
1990
High resolution mapping of consistent leiomyoma breakpoints in chromosomes 12 and 14 to 12q15 and 14q24.1
A substantial percentage of uterine leiomyomas are cytogenetically characterized by consistent, clonal chromosome abnormalities… 
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