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3p21.2

A chromosome band present on 3p
National Institutes of Health

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3 relations
Chromosome 3 Short ArmChromosomesGRM2 wt Allele

Papers overview

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2017
2017
Biallelic loss‐of‐function variants in DOCK3 cause muscle hypotonia, ataxia, and intellectual disability
DOCK3 encodes the dedicator of cytokinesis 3 protein, a member of the DOCK180 family of proteins that are characterized by… 
2005
2005
Chromosome 3p alterations in northeastern Thai women with cervical carcinoma.
The purpose of this study was to determine the incidence of the loss of heterozygosity (LOH) among normal cervixes, cervical… 
2004
2004
Identification and expression of a novel human testis-specific gene by digital differential display.
BACKGROUND Evidence for the importance of genetic factors in male infertility is accumulating. This study was designed to… 
2003
2003
Zimmermann–Laband syndrome associated with a balanced reciprocal translocation t(3;8)(p21.2;q24.3) in mother and daughter: Molecular cytogenetic characterization of the breakpoint regions
Zimmermann–Laband syndrome (ZLS) is a rare disorder characterized by gingival fibromatosis, abnormalities of the nose and/or ears… 
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… 
2001
2001
Interstitial deletion of 3p22.2-p24.2: the first reported case
Autosomal deletions or chromosomal haploinsufficiency syndromes are observed in 1 in 7000 live born infants1 and may cause… 
1998
1998
Loss of heterozygosity at chromosome 3p correlates with telomerase activity in renal cell carcinoma.
Acquired loss of the entire or parts of the short arm of chromosome 3 is a frequent aberration in renal cell carcinoma as well as… 
Review
1998
Review
1998
Assignment1 of inosine ′-monophosphate dehydrogenase type 2 (IMPDH2) to human chromosome band 3p21.2 by in situ hybridization
Inosine 5)-monophosphate dehydrogenase (IMPDH, E.C. 1.1.1.205) is the rate limiting enzyme in de novo guanine nucleotide… 
1996
1996
Amplification of the Transketolase Gene in Desensitization-resistant Mutant Y1 Mouse Adrenocortical Tumor Cells (*)
As shown previously, mutants of the Y1 mouse adrenocortical tumor cell line that resist agonist-induced desensitization of… 
1995
1995
Localization of human ARF2 and NCK genes and 13 other NotI-linking clones to chromosome 3 by fluorescence in situ hybridization.
Two human genes containing NotI sites, ADP-ribosylation factor (ARF2) and melanoma NCK protein, were mapped by fluorescence in… 
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