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Chromosomes, Human, Pair 20

Known as: 20 chromosome, Chromosome 20 
The designation for each member of the third smallest human autosomal chromosome pair. Chromosome 20 spans around 63 million base pairs and… 
National Institutes of Health

Related topics

Related topics

25 relations
20qAAR2 geneC20orf24 geneC20orf27 gene

Narrower (3)

Chromosome 20, deletion 20pChromosome 20, trisomyTrisomy 20p

Broader (1)

Chromosomes, Human, 19-20

Papers overview

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Highly Cited
2003
Highly Cited
2003
Malignant brain tumor repeats: a three-leaved propeller architecture with ligand/peptide binding pockets.
Highly Cited
2002
Highly Cited
2002
A region of chromosome 20 is linked to leprosy susceptibility in a South Indian population.
A major susceptibility locus for leprosy has recently been mapped on chromosome 10 (10p13) by genome-wide linkage analysis… 
Highly Cited
2001
Highly Cited
2001
Efficient male and female germline transmission of a human chromosomal vector in mice.
A small accessory chromosome that was mitotically stable in human fibroblasts was transferred into the hprt(-) hamster cell line… 
Highly Cited
1999
Highly Cited
1999
Parent-offspring trios: a resource to facilitate the identification of type 2 diabetes genes.
The transmission disequilibrium test with use of trios (an affected proband with both parents) is a robust method for assessing… 
Highly Cited
1998
Highly Cited
1998
Delineation of supernumerary marker chromosomes in 38 patients.
We present cytogenetic and clinical data on 38 patients with supernumerary marker chromosomes (SMCs). SMCs were characterized… 
Highly Cited
1996
Highly Cited
1996
Hematologic disorders associated with deletions of chromosome 20q: a clinicopathologic study of 107 patients.
To study the pathogenetic significance of acquired del(20q), bone marrow morphology and clinical histories of 107 patients with… 
Highly Cited
1992
Highly Cited
1992
Gene structure of semenogelin I and II. The predominant proteins in human semen are encoded by two homologous genes on chromosome 20.
Highly Cited
1991
Highly Cited
1991
G protein Gs alpha (GNAS 1), the probable candidate gene for Albright hereditary osteodystrophy, is assigned to human chromosome 20q12-q13.2.
1991
1991
Chromosomal assignments of the genes for neuroendocrine convertase PC1 (NEC1) to human 5q15-21, neuroendocrine convertase PC2 (NEC2) to human 20p11.1-11.2, and furin (mouse 7[D1-E2] region).
Highly Cited
1984
Highly Cited
1984
Hematologic manifestations associated with deletions of the long arm of chromosome 20.
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