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2q21.3
A chromosome band present on 2q.
National Institutes of Health
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Related topics
Related topics
3 relations
Chromosomes
MIR128-1 wt Allele
ZRANB3 wt Allele
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2019
2019
Lactase Persistence in Southern Iberia and Northwestern Africa: New Insights into the Population Structure and History of Western Mediterranean
R. Calderón
2019
Corpus ID: 204055934
The development of lactose tolerance in humans represents a fair example of interaction between biology and culture. Lactase…
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Review
2016
Review
2016
Genetics in Keratoconus: where are we?
Y. Bykhovskaya
,
Benjamin Margines
,
Y. Rabinowitz
Eye and Vision
2016
Corpus ID: 17887878
Keratoconus (KC) is a non-inflammatory thinning and protrusion of the cornea in which the cornea assumes a conical shape. Complex…
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Highly Cited
2015
Highly Cited
2015
SnapShot: Genetics of Parkinson’s Disease
J. Bras
,
R. Guerreiro
,
J. Hardy
Cell
2015
Corpus ID: 13962717
2013
2013
Angelman syndrome and severe infections in a patient with de novo 15q11.2-q13.1 deletion and maternally inherited 2q21.3 microdeletion.
Gerda Neubert
,
K. von Au
,
+4 authors
A. Kaindl
Gene
2013
Corpus ID: 24840479
2013
2013
[Anaplastic large cell lymphoma: an array-based comparative genomic hybridization study].
Miao Wang
,
Ran Liu
,
Li Su
,
R. Yu
,
L. Gong
Zhonghua bing li xue za zhi = Chinese journal of…
2013
Corpus ID: 26104991
OBJECTIVE To use array-based comparative genomic hybridization (aCGH) technology to study the molecular cytogenetic abnormalities…
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Highly Cited
2012
Highly Cited
2012
A genome-wide association study identifies a potential novel gene locus for keratoconus, one of the commonest causes for corneal transplantation in developed countries.
Xiaohui Li
,
Y. Bykhovskaya
,
+7 authors
Y. Rabinowitz
Human molecular genetics
2012
Corpus ID: 13320773
Keratoconus is a condition in which the cornea progressively thins over time, and is a major cause for cornea transplantation. To…
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2012
2012
Use of germline polymorphisms in predicting concurrent chemoradiotherapy response in esophageal cancer.
Pei-Chun Chen
,
Yen-Ching Chen
,
+7 authors
E. Chuang
International journal of radiation oncology…
2012
Corpus ID: 11339351
2008
2008
A single nucleotide polymorphism at chromosome 2q21.3 (LCT -13910C>T) associates with clinical outcome after allogeneic hematopoietic stem cell transplantation.
Hanns Hauser
,
O. Zach
,
+5 authors
D. Lutz
Blood
2008
Corpus ID: 206868877
A single nucleotide polymorphism (SNP) responsible for lactase persistence (LCT -13910C>T) changes intestinal microflora…
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Review
2006
Review
2006
Prenatal diagnosis of de novo interstitial 2q14.2-2q21.3 deletion assisted by array-based comparative genomic hybridization: a case report.
H. Peng
,
Chin-Jung Wang
,
Tzu-Hao Wang
,
Shuenn-Dyh Chang
The Journal of reproductive medicine
2006
Corpus ID: 25966773
BACKGROUND During conventional karyotyping, it can be difficult to clearly identify de novo interstitial deletion of a…
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1987
1987
Chromosome studies in inherited nonpolyposis colon cancer syndrome.
R. Lukeis
,
O. Garson
,
F. Macrae
,
D. S. St. John
,
R. Whitehead
Cancer genetics and cytogenetics
1987
Corpus ID: 30549106
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