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21q22.3
A chromosome band present on 21q
National Institutes of Health
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Related topics
Related topics
23 relations
21q
ABCG1 wt Allele
AIRE wt Allele
BACE2 wt Allele
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Highly Cited
2007
Highly Cited
2007
Recessive congenital total cataract with microcornea and heterozygote carrier signs caused by a novel missense CRYAA mutation (R54C).
Arif O. Khan
,
Mohammad A. Aldahmesh
,
B. Meyer
American journal of ophthalmology-glaucoma
2007
Corpus ID: 37857507
2000
2000
Mapping of a new target region of allelic loss at 21q22 in primary gastric cancers.
W. Park
,
Ro Ra Oh
,
+9 authors
Jung Young Lee
Cancer Letters
2000
Corpus ID: 723622
2000
2000
Cloning and characterization of a putative human glycerol 3-phosphate permease gene (SLC37A1 or G3PP) on 21q22.3: mutation analysis in two candidate phenotypes, DFNB10 and a glycerol kinase…
L. Bartoloni
,
M. Wattenhofer
,
+14 authors
S. Antonarakis
Genomics
2000
Corpus ID: 9876639
Using multiple exons trapped from human chromosome 21 (HC21)-specific cosmids with homology to a putative Arabidopsis thaliana…
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1998
1998
The gene responsible for autoimmune polyglandular syndrome type 1 maps to chromosome 21q22.3 in US patients.
Q. Chen
,
Michael S. Lan
,
J. She
,
Noel K. Maclaren
Journal of Autoimmunity
1998
Corpus ID: 2521150
Autoimmune polyglandular syndrome type 1 [APS-1] comprises multiple organ-specific autoimmunities such as acquired…
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1998
1998
Identification and characterization of a new human cDNA from chromosome 21q22.3 encoding a basic nuclear protein
A. Egeo
,
M. Mazzocco
,
+6 authors
P. Scartezzini
Human Genetics
1998
Corpus ID: 11629055
Congenital heart disease (CHD) affects over 40% of Down syndrome (DS) patients. The region proposed to contain the gene(s) for DS…
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1998
1998
Construction of a 2.5-Mb integrated physical and gene map of distal 21q22.3.
V. Lapenta
,
V. Sossi
,
+9 authors
C. Brahe
Genomics
1998
Corpus ID: 19249570
The gene-rich telomeric region of 21q harbors several loci relevant to human diseases including autoimmune polyglandular disease…
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1996
1996
The gene for human U2 snRNP auxiliary factor small 35-kDa subunit (U2AF1) maps to the progressive myoclonus epilepsy (EPM1) critical region on chromosome 21q22.3.
M. Lalioti
,
A. Gos
,
M. Green
,
C. Rossier
,
M. Morris
,
S. Antonarakis
Genomics
1996
Corpus ID: 10089787
We used targeted exon trapping to clone portions of genes from human chromosome 21q22.3. One trapped sequence showed complete…
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1995
1995
Localization of cDNAs to a region poorly represented in the CEPH chromosome 21 YAC contig: candidate genes for genetic diseases mapped to 21q22.3.
K. Gardiner
,
H. Ichikawa
,
M. Ohki
,
D. Patterson
,
J. Cheng
Genomics
1995
Corpus ID: 9218422
Fifty-three cDNA fragments previously obtained by hybridization selection from random clones in the chromosome 21 cosmid library…
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1994
1994
Comparison of chromosome aberrations in leiomyoma and leiomyosarcoma using FISH on archival tissues.
K. Han
,
W. Lee
,
+4 authors
L. Meisner
Cancer Genetics and Cytogenetics
1994
Corpus ID: 3429875
Highly Cited
1986
Highly Cited
1986
Regional localization of DNA sequences on chromosome 21 using somatic cell hybrids.
M. V. Van Keuren
,
P. Watkins
,
H. Drabkin
,
E. Jabs
,
J. Gusella
,
D. Patterson
American Journal of Human Genetics
1986
Corpus ID: 7202100
We have used a panel of Chinese hamster X human somatic cell hybrids, each containing various portions of chromosome 21 as the…
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