Skip to search form
Skip to main content
Skip to account menu
Semantic Scholar
Semantic Scholar's Logo
Search 227,741,321 papers from all fields of science
Search
Sign In
Create Free Account
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…
Expand
National Institutes of Health
Create Alert
Alert
Related topics
Related topics
25 relations
20q
AAR2 gene
C20orf24 gene
C20orf27 gene
Expand
Narrower (3)
Chromosome 20, deletion 20p
Chromosome 20, trisomy
Trisomy 20p
Broader (1)
Chromosomes, Human, 19-20
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
Highly Cited
2003
Highly Cited
2003
Malignant brain tumor repeats: a three-leaved propeller architecture with ligand/peptide binding pockets.
W. Wang
,
V. Tereshko
,
P. Boccuni
,
D. MacGrogan
,
S. Nimer
,
D. Patel
Structure
2003
Corpus ID: 23010272
Highly Cited
2002
Highly Cited
2002
A region of chromosome 20 is linked to leprosy susceptibility in a South Indian population.
K. Tosh
,
S. Meisner
,
+6 authors
Adrian V.S. Hill
Journal of Infectious Diseases
2002
Corpus ID: 11889483
A major susceptibility locus for leprosy has recently been mapped on chromosome 10 (10p13) by genome-wide linkage analysis…
Expand
Highly Cited
2001
Highly Cited
2001
Efficient male and female germline transmission of a human chromosomal vector in mice.
T. Voet
,
J. Vermeesch
,
+5 authors
P. Marynen
Genome Research
2001
Corpus ID: 36068166
A small accessory chromosome that was mitotically stable in human fibroblasts was transferred into the hprt(-) hamster cell line…
Expand
Highly Cited
1999
Highly Cited
1999
Parent-offspring trios: a resource to facilitate the identification of type 2 diabetes genes.
T. Frayling
,
Mark Walker
,
+11 authors
A. Hattersley
Diabetes
1999
Corpus ID: 5677889
The transmission disequilibrium test with use of trios (an affected proband with both parents) is a robust method for assessing…
Expand
Highly Cited
1998
Highly Cited
1998
Delineation of supernumerary marker chromosomes in 38 patients.
R. Viersbach
,
H. Engels
,
U. Gamerdinger
,
M. Hansmann
American journal of medical genetics
1998
Corpus ID: 27418961
We present cytogenetic and clinical data on 38 patients with supernumerary marker chromosomes (SMCs). SMCs were characterized…
Expand
Highly Cited
1996
Highly Cited
1996
Hematologic disorders associated with deletions of chromosome 20q: a clinicopathologic study of 107 patients.
Paul J. Kurtin
,
G. Dewald
,
D. Shields
,
C. Hanson
American Journal of Clinical Pathology
1996
Corpus ID: 11410547
To study the pathogenetic significance of acquired del(20q), bone marrow morphology and clinical histories of 107 patients with…
Expand
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.
M. Ulvsbäck
,
C. Lazure
,
+5 authors
Å. Lundwall
Journal of Biological Chemistry
1992
Corpus ID: 43738240
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.
V. G. GOPAL RAO
,
Susanne Schnittger
,
I. Hansmann
Genomics
1991
Corpus ID: 13249544
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).
N. Seidah
,
M. Mattei
,
László Gáspár
,
S. Benjannet
,
M. Mbikay
,
M. Chrétien
Genomics
1991
Corpus ID: 34201335
Highly Cited
1984
Highly Cited
1984
Hematologic manifestations associated with deletions of the long arm of chromosome 20.
Mellar P. Davis
,
G. Dewald
,
R. Pierre
,
H. Hoagland
Cancer Genetics and Cytogenetics
1984
Corpus ID: 3435900
By clicking accept or continuing to use the site, you agree to the terms outlined in our
Privacy Policy
(opens in a new tab)
,
Terms of Service
(opens in a new tab)
, and
Dataset License
(opens in a new tab)
ACCEPT & CONTINUE