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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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2009
2009
Further characterization of a somatic cell hybrid panel: ten new assignments to the bovine genome.
Thirty-six partially characterized hamster-bovine hybrid cell lines were used for the determination of synteny groups. Sixteen… 
2009
2009
A child with partial trisomy 7 and 20 inherited from the mother.
A child with partial trisomy of the long arm of chromosome 7 and the short arm of chromosome 20 is described. The aberration was… 
Review
2005
Review
2005
Genetic Analysis of HNF 4 A Polymorphisms in Caucasian-American Type 2 Diabetes
Hepatocyte nuclear factor 4 (HNF4A), the gene for the maturity-onset diabetes of the young type 1 monogenic form of type 2… 
1987
1987
Localization and linkage of three polymorphic DNA sequences on human chromosome 20.
The D20S6 locus has been sublocalized by in situ hybridization using the pD3H12 probe to human chromosome band 20p12 and the… 
1987
1987
Detection of human DNA polymorphisms with a simplified denaturing gradient gel electrophoresis technique.
Single base pair differences between otherwise identical DNA molecules can result in altered melting behavior detectable by… 
1985
1985
In vitro growth and chromosome constitution of placental cells. II. Hydatidiform moles.
Histopathological features, in vitro growth, and cytogenetic characteristics of tissue samples from molar placentae were studied… 
1981
1981
Partial trisomy 20.
A child with a facial dysmorphy and congenital malformations, showed in the chromosome analysis a partial trisomy of chromosome… 
1978
1978
Deletion of the long arm of chromosome 20 [del(20)(q11)] in myeloid disorders.
Detailed clinical and cytogenetic studies were performed in five patients who had abnormal hematopoiesis and an acquired deletion… 
1976
1976
Assignment of inosine triphosphatase gene to gorilla chromosome 13 and to human chromosome 20 in primate-rodent somatic cell hybrids.
1976
1976
Confirmation of the assignment of the locus determining ADA to chromosome 20 in man: data on possible synteny of ADA and ITP in human-Chinese hamster somatic cell hybrids.