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16q21

A chromosome band present on 16q
National Institutes of Health

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6 relations
16qAMFR wt AlleleCDH11 wt AlleleCETP wt Allele

Papers overview

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2015
2015
Genetic variants at 6p21, 10q23, 16q21 and 22q12 are associated with esophageal cancer risk in a Chinese Han population.
OBJECTIVE A number of recently published genome-wide association studies (GWAS) identified several genetic loci at 6p21, 10q23… 
2015
2015
Genetic variants at 6 p 21 , 10 q 23 , 16 q 21 and 22 q 12 are associated with esophageal cancer risk in a Chinese Han population
Objective: A number of recently published genome-wide association studies (GWAS) identified several genetic loci at 6p21, 10q23… 
2013
2013
Distinctive neurological phenotype associated with partial trisomy of chromosome 16.
2004
2004
Analysis of 6 genetic loci for disease susceptibility in psoriatic arthritis.
OBJECTIVE To analyze the association of several autoimmune disease susceptibility loci in a population of patients with psoriasis… 
2001
2001
Chromosome 16q deletion and loss of E‐cadherin expression in Hodgkin and Reed‐Sternberg cells
Hodgkin and Reed‐Sternberg (H&RS) cells are generally considered to be the neoplastic cells of Hodgkin's disease (HD); however… 
1997
1997
Allelic imbalance mapping of chromosome 16 shows two regions of common deletion in prostate adenocarcinoma.
Highly Cited
1996
Highly Cited
1996
Linkage of Gitelman syndrome to the thiazide-sensitive sodium-chloride cotransporter gene with identification of mutations in Dutch families
Abstract. Gitelman syndrome is a mostly autosomal recessive disorder affecting the renal tubular function associated with… 
1995
1995
A constitutional bws‐related t(11;16) chromosome translocation occurring in the same region of chromosome 16 implicated in wilms' tumors
Beckwith‐Wiedemann syndrome (BWS) is a congenital overgrowth disorder with a varying spectrum of clinical manifestations… 
1989
1989
Gene mapping on chorionic villi chromosomes by hybridization in situ: localization of cholinesterase cDNA binding sites to chromosomes 3q21, 3q26-ter and 16q21.
To adapt the in-situ hybridization approach for use in very early fetal development, comparative in-situ hybridization was… 
1976
1976
Constitutional chromosomal breakage
SummaryThere were 18 individuals found to have a constitutional chromosome fragility causing an increase in break frequency. For… 
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