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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…
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National Institutes of Health
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Related topics
Related topics
38 relations
13q
Aleukemic Chronic Lymphocytic Leukemia
Chromatin
Chromosome 13 Short Arm
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Narrower (6)
Chromosome 13 ring
Chromosome 13q deletion syndrome
Chromosome 13q trisomy
Patau syndrome
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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).
I. Garkavtsev
,
D. Demetrick
,
K. Riabowol
Cytogenetics and Cell Genetics
1997
Corpus ID: 46839265
A novel gene called ING1 encoding a 33-kDa protein that is an inhibitor of cell growth and a candidate tumor suppressor has been…
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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.
H. Chaib
,
G. Lina-Granade
,
+4 authors
C. Petit
Human Molecular Genetics
1994
Corpus ID: 33046013
The first localization of a gene responsible for autosomal, neurosensory, recessive deafness recently assigned NSRD1 to the…
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Highly Cited
1992
Highly Cited
1992
The human 5-HT2 receptor is encoded by a multiple intron-exon gene.
K. Chen
,
W. Yang
,
J. Grimsby
,
J. Shih
Brain Research. Molecular Brain Research
1992
Corpus ID: 29143868
Highly Cited
1989
Highly Cited
1989
Structure and partial genomic sequence of the human retinoblastoma susceptibility gene.
T. L. McGee
,
D. Yandell
,
T. Dryja
Gene
1989
Corpus ID: 8728029
Highly Cited
1984
Highly Cited
1984
Nonrandom chromosomal changes in transitional cell carcinoma of the bladder.
Z. Gibas
,
Prout Gr
,
Connolly Jg
,
Pontes Je
,
A. Sandberg
Cancer Research
1984
Corpus ID: 15133054
Nine cases of transitional cell carcinoma (eight from the urinary bladder and one from the ureter; six noninvasive and three…
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Highly Cited
1984
Highly Cited
1984
Isolation and regional localization of DNA segments revealing polymorphic loci from human chromosome 13.
W. Cavenee
,
R. Leach
,
T. Mohandas
,
P. Pearson
,
R. White
American Journal of Human Genetics
1984
Corpus ID: 46016830
A recombinant DNA library enriched for portions of human chromosome 13 has been constructed from a hamster-human somatic cell…
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Highly Cited
1981
Highly Cited
1981
Familial retinoblastoma and chromosome 13 deletion transmitted via an insertional translocation.
L. Strong
,
V. Riccardi
,
R. Ferrell
,
R. Sparkes
Science
1981
Corpus ID: 43756256
Surviving persons from a kindred in which retinoblastoma occurred over four generations, transmitted by eight unaffected…
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Highly Cited
1978
Highly Cited
1978
Partial Trisomies and Deletions of Chromosome 13
R. Coco
,
G. Rey
Pediatric Research
1978
Corpus ID: 46261086
With the advent of new banding techniques there have been increasing numbers of patients with trisomies and deletions for…
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Highly Cited
1976
Highly Cited
1976
Partial deletions and trisomies of chromosome 13; Mapping of bands associated with particular malformations
B. Noel
,
B. Quack
,
M. Rethoré
Clinical Genetics
1976
Corpus ID: 37135694
New techniques of human karyotyping have allowed us to define accurately the banding pattern of six new cases with partial…
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Highly Cited
1974
Highly Cited
1974
Human Chromosome 21 Dosage: Effect on the Expression of the Interferon Induced Antiviral State
Y. H. Tan
,
Edward L. Schneider
,
Jay A. Tischfield
,
Charles J. Epstein
,
Frank H. Ruddle
Science
1974
Corpus ID: 21964342
Human primary skin fibroblasts trisomic for chromosome 13, 18, or 21 and diploid human skin fibroblasts were induced for an…
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