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2p21
A chromosome band present on 2p
National Institutes of Health
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7 relations
COX7A2L wt Allele
Chromosome 2 Short Arm
Chromosomes
EPCAM wt Allele
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Papers overview
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2019
2019
Toward Primary Congenital Glaucoma GLC 3 B Gene Identification : The Case of Kazrin Gene
Soumaya El Akil
,
A. Belmouden
2019
Corpus ID: 76649518
Primary Congenital Glaucoma (PCG) is an ocular disease that occurs before the age of 3 years, and results from malformation of…
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2018
2018
Genomic Changes in Pediatric Renal Transplant Patients Detected by aCGH
Y. Terzi
,
F. Sahin
,
+4 authors
M. Haberal
Transplantation
2018
Corpus ID: 81335888
Introduction Acute and chronic allograft rejection are major problems in kidney transplantation. Identifying differences among…
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2013
2013
Spnb2 Protein Family Architecture Perspective and Differences in Complex Form of Exon/intron Usage
Mark R. Brenneman
2013
Corpus ID: 83011823
Spectrin isoforms are found in erythroid and nonerythroid cells. Spectrin is a component (known as the postsynaptic density (PSD…
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2013
2013
Comment on Kanaji et al , page 2732 Sitosterolemia : platelets on high-sterol diet---------------------------------------------------------------------------------------------------- -
H. Falet
2013
Corpus ID: 22384338
S itosterolemia is a rare inherited lipid metabolic disorder characterized by the presence of xanthomas, premature coronary…
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2010
2010
Genetics: Novel prostate cancer susceptibility loci
Nick Groves-Kirkby
Nature reviews. Urology
2010
Corpus ID: 41402084
Prostate cancer shows significant familial association, but known loci have small effects on disease susceptibility, and…
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2010
2010
A polymorphism in the CYP 1 B 1 promoter is functionally associated with primary congenital glaucoma
S. Chakrabarti
,
Y. Ghanekar
,
+6 authors
P. Majumder
2010
Corpus ID: 3376988
Primary congenital glaucoma (PCG) is a childhood autosomal-recessive disorder caused by developmental defects in the trabecular…
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Review
2007
Review
2007
Fibromatose gengival hereditária: identificação e tratamento Hereditary Gingival Fibromatosis: Identification and treatment
M. Serra
,
M. E. V. Falabella
,
E. Tinoco
,
M. Ribeiro
,
D. G. Silva
,
Júlia do Monte Souto Maior
2007
Corpus ID: 56388119
Hereditary gingival fibromatosis (HGF) is described as a rare oral condition, clinically manifested by a slow, progressive and…
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2006
2006
Cytogenetic Profile of 109 Lipomas 1
Chandrika
,
Sreekantaiah
,
+12 authors
A. Sandberg
2006
Corpus ID: 16693262
Cytogenetic analysis of short-term cultures was carried out on 109 lipomas from 92 patients. Clonal chromosomal abnormalities…
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2006
2006
Cytogenetic Profile of 109 Lipomas Updated
Chandrika
,
Sreekantaiah
,
+12 authors
A. Sandberg
2006
Corpus ID: 6069058
Cytogenetic analysis of short-term cultures was carried out on 109 lipomas from 92 patients. Clonal chromosomal abnormalities…
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2006
2006
Constructing Association Network in Tw o Stage Analysis: An Application of Backward Genotype-Trait Associati on (BGTA) Algorithm to NARAC Data
Yuejing Ding
,
T. Zheng
,
I. Ionita-Laza
,
Lei Cong
,
S. Lo
2006
Corpus ID: 10510146
In this paper, we applied the Backward Genotype-Trait Association (BGTA) algorithm to capture both the marginal and gene-gene…
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