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3p21.33

A chromosome band present on 3p.
National Institutes of Health

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Chromosomes

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2016
2016
Association of the chromosome 11p13.5 variant and atopic dermatitis with a family history of atopy in the Chinese Han population.
BACKGROUND Recent genome-wide association studies (GWAS) and a meta-analysis of GWAS for atopic dermatitis (AD) have identified… 
2016
2016
Association of the chromosome 11 p 13 . 5 variant and atopic dermatitis with a family history of atopy in the Chinese Han population
Results: We found that rs12634229 (3q13.2), rs7927894 (11p13.5) and rs878860 (11p15.4) showed a slight association with AD (P = 0… 
2005
2005
[NotI-STS markers for human chromosome 3 are gene markers].
Ninety four NotI-STS markers to seventy two individual NotI clones were developed basing on DNA nucleotide sequences from NotI… 
2005
2005
NotI Sequence-Tagged Sites as Markers of Genes on Human Chromosome 3
Using nucleotide sequences from jumping and linking NotI libraries of human chromosome 3, 94 NotI-STS markers for 72 individual… 
2003
2003
Multiple Deletions in Chromosome 3p are Associated with the Development of Head and Neck Squamous Cell Carcinoma
Abstract Detailed deletion mapping was done in the chromosomal 3p21.2-22 and 3p12-13 regions, showing high deletions in our… 
2002
2002
Delimitation of duplicated segments and identification of their parental origin in two partial chromosome 3p duplications.
Two chromosome 3 short arm duplications identified through G-banding were further investigated using fluorescence in situ… 
1993
1993
Assignment of human β-galactosidase-A gene to 3p21.33 by fluorescence in situ hybridization
GM1 gangliosidosis and Morquio syndrome type B (MPS IVB) are inherited lyosomal storage disorders associated with deficiency of… 
1993
1993
Assignment of human beta-galactosidase-A gene to 3p21.33 by fluorescence in situ hybridization.
GM1 gangliosidosis and Morquio syndrome type B (MPS IVB) are inherited lyosomal storage disorders associated with deficiency of… 
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