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Chromosomes, Human, Pair 13

Known as: 13 chromosome, 13 chromosomes, Chromosome 13 
The designation for each member of the thirteenth largest human autosomal chromosome pair. Chromosome 13 spans about 113 million base pairs and… 
National Institutes of Health

Related topics

Related topics

38 relations
13qAleukemic Chronic Lymphocytic LeukemiaChromatinChromosome 13 Short Arm

Narrower (6)

Chromosome 13 ringChromosome 13q deletion syndromeChromosome 13q trisomyPatau syndrome

Broader (1)

Chromosomes, Human, 13-15

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
Highly Cited
1997
Highly Cited
1997
Cellular localization and chromosome mapping of a novel candidate tumor suppressor gene (ING1).
A novel gene called ING1 encoding a 33-kDa protein that is an inhibitor of cell growth and a candidate tumor suppressor has been… 
Highly Cited
1994
Highly Cited
1994
A gene responsible for a dominant form of neurosensory non-syndromic deafness maps to the NSRD1 recessive deafness gene interval.
The first localization of a gene responsible for autosomal, neurosensory, recessive deafness recently assigned NSRD1 to the… 
Highly Cited
1992
Highly Cited
1992
The human 5-HT2 receptor is encoded by a multiple intron-exon gene.
Highly Cited
1989
Highly Cited
1989
Structure and partial genomic sequence of the human retinoblastoma susceptibility gene.
Highly Cited
1984
Highly Cited
1984
Nonrandom chromosomal changes in transitional cell carcinoma of the bladder.
Nine cases of transitional cell carcinoma (eight from the urinary bladder and one from the ureter; six noninvasive and three… 
Highly Cited
1984
Highly Cited
1984
Isolation and regional localization of DNA segments revealing polymorphic loci from human chromosome 13.
A recombinant DNA library enriched for portions of human chromosome 13 has been constructed from a hamster-human somatic cell… 
Highly Cited
1981
Highly Cited
1981
Familial retinoblastoma and chromosome 13 deletion transmitted via an insertional translocation.
Surviving persons from a kindred in which retinoblastoma occurred over four generations, transmitted by eight unaffected… 
Highly Cited
1978
Highly Cited
1978
Partial Trisomies and Deletions of Chromosome 13
With the advent of new banding techniques there have been increasing numbers of patients with trisomies and deletions for… 
Highly Cited
1976
Highly Cited
1976
Partial deletions and trisomies of chromosome 13; Mapping of bands associated with particular malformations
New techniques of human karyotyping have allowed us to define accurately the banding pattern of six new cases with partial… 
Highly Cited
1974
Highly Cited
1974
Human Chromosome 21 Dosage: Effect on the Expression of the Interferon Induced Antiviral State
Human primary skin fibroblasts trisomic for chromosome 13, 18, or 21 and diploid human skin fibroblasts were induced for an… 
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