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Chromosomes, Human, Pair 12

Known as: 12 chromosome, Chromosome 12 
The designation for each member of the twelfth largest human autosomal chromosome pair. Chromosome 12 spans about 143 million base pairs and… 
National Institutes of Health

Related topics

Related topics

34 relations
12qAleukemic Chronic Lymphocytic LeukemiaAtypical LipomaCSRNP2 gene

Narrower (3)

Chromosome 12, 12p trisomyChromosome 12, trisomy 12qPallister-Killian syndrome

Broader (1)

Chromosomes, Human, 6-12 and X

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
Highly Cited
2008
Highly Cited
2008
Variants in the neuronal nitric oxide synthase (nNOS, NOS1) gene are associated with restless legs syndrome
Sixty percent of the patients with restless legs syndrome (RLS) report a positive family history. To date five loci have been… 
Highly Cited
2001
Highly Cited
2001
Comparative sequence analysis of the imprinted Dlk1-Gtl2 locus in three mammalian species reveals highly conserved genomic elements and refines comparison with the Igf2-H19 region.
The Dlk1-Gtl2 domain on mouse chromosome 12 contains reciprocally imprinted genes with the potential to contribute to our… 
Highly Cited
1998
Highly Cited
1998
American families with Crohn's disease have strong evidence for linkage to chromosome 16 but not chromosome 12.
Highly Cited
1994
Highly Cited
1994
Fluorescence in situ hybridization mapping of translocations and deletions involving the short arm of human chromosome 12 in malignant hematologic diseases.
Translocations and deletions of the short arm of chromosome 12 [t(12p) and del(12p)] are common recurring abnormalities in a… 
Highly Cited
1991
Highly Cited
1991
Characterization of an alpha 1----3-galactosyltransferase homologue on human chromosome 12 that is organized as a processed pseudogene.
UDP-Gal:Gal beta 1----4GlcNAc alpha 1----3-galactosyltransferase is a terminal glycosyltransferase that is widely expressed in a… 
Highly Cited
1990
Highly Cited
1990
Molecular cloning, functional expression, and chromosomal localization of mouse hepatocyte nuclear factor 1.
The homeodomain-containing transcription factor hepatocyte nuclear factor 1 (HNF-1) most likely plays an essential role during… 
Highly Cited
1990
Highly Cited
1990
Cytogenetic analysis of human solid tumors by in situ hybridization with a set of 12 chromosome-specific DNA probes.
We have applied fluorescent in situ hybridization (FISH) to assess the presence of numerical chromosome aberrations in fresh… 
Highly Cited
1987
Highly Cited
1987
A primary genetic linkage map for human chromosome 12.
Highly Cited
1977
Highly Cited
1977
Gene mapping in Mus musculus by interspecific cell hybridization: assignment of the genes for tripeptidase-1 to chromosome 10, dipeptidase-2 to chromosome 18, acid phosphatase-1 to chromosome 12, and…
Chinese hamster X mouse somatic cell hybrids segregating mouse chromosomes were examined for their mouse chromosome content using… 
Highly Cited
1977
Highly Cited
1977
Chromosome mapping of the genes that control differentiation and malignancy in myeloid leukemic cells.
The chromosome banding pattern has been analyzed in clones of mouse myeloid leukemic cells that differ in their ability to be… 
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