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12q13

A chromosome band present on 12q
National Institutes of Health

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20 relations
12qACVR1B wt AlleleAMHR2 wt AlleleATF1 wt Allele

Papers overview

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2004
2004
Heritable fragile sites on human chromosomes
SummaryThe fragile site at Xq27 which is associated with X-linked mental retardation with macroorchidism has been studied in 21… 
Highly Cited
1997
Highly Cited
1997
Amplification of multiple regions of chromosome 12, including 12q13–15, in chronic lymphocytic leukaemia
Abstract: Trisomy 12 is a frequent abnormality in chronic lymphocytic leukaemia (CLL). The biological importance of trisomy 12 is… 
Highly Cited
1994
Highly Cited
1994
Organization of the human keratin type II gene cluster at 12q13.
Keratin proteins constitute intermediate filaments and are the major differentiation products of mammalian epithelial cells. The… 
1992
1992
Chromosome abnormalities in liposarcomas.
1992
1992
Supernumerary ring marker chromosome as a secondary rearrangement in a parapharyngeal lipoma with t(10;12)(q25;q15) as the primary karyotypic abnormality.
Review
1990
Review
1990
Chromosomal patterns in human benign uterine leiomyomas.
Highly Cited
1989
Highly Cited
1989
Chromosomal abnormalities in Hodgkin's disease.
Numerous neoplastic states have associated or causal cytogenetic abnormalities. In some cancers, specific chromosomal… 
1989
1989
The gene for the human putative apoE receptor is on chromosome 12 in the segment q13-14.
1988
1988
Chromosome localization of the human oncogene INT1 to 12q13 by in situ hybridization.
The human oncogene INT1 has been mapped to chromosome band 12q13 by in situ hybridization. The precise localization of this gene… 
1987
1987
The human int-1 gene is located at chromosome region 12q12-12q13 and is not rearranged in myxoid liposarcoma with t(12;16) (q13;p11).
The mouse cellular oncogene int-1 is often transcriptionally activated as a consequence of nearby proviral insertions in mouse… 
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