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22q13.31

A chromosome band present on 22q.
National Institutes of Health

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Related topics

5 relations
CERK wt AlleleChromosomesHDAC10 wt AlleleMIRLET7A3 wt Allele

Papers overview

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2015
2015
PHF21B as a candidate tumor suppressor gene in head and neck squamous cell carcinomas
2013
2013
Genome-wide Linkage and Regional Association Study of Obesity-related Phenotypes: The GenSalt study
To identify chromosomal regions harboring quantitative trait loci for waist circumference (WC) and body mass index (BMI). 
2012
2012
A Pilot Study on Collective Effects of 22q13.31 Deletions on Gray Matter Concentration in Schizophrenia
The association of copy number variation (CNV) with schizophrenia has been reported with evidence of increased frequency of both… 
2010
2010
Evidence against haploinsuffiency of human ataxin 10 as a cause of spinocerebellar ataxia type 10
Spinocerebellar ataxia type 10 (SCA10) is an autosomal dominant neurodegenerative disorder characterized by ataxia and cerebellar… 
2010
2010
Fulminant hepatic failure requiring liver transplantation in 22q13.3 deletion syndrome
We report on a 4‐year‐old girl with severe developmental delay, absent speech, and chromosome 22q13.3 deletion (Phelan–McDermid… 
2008
2008
A cryptic duplication 22q13.31 to qter leads to a distinct phenotype with mental retardation, microcephaly and mild facial dysmorphism.
We present a girl with a terminal 22q duplication due to an unbalanced chromosomal translocation: 46, XX, der(22)(qter --> q13.31… 
2006
2006
Novel candidate tumour suppressor gene loci on chromosomes 11q23–24 and 22q13 involved in human insulinoma tumourigenesis
Insulinomas represent the predominant syndromic subtype of endocrine pancreatic tumours. Previous molecular studies have shown… 
2005
2005
PRR5 encodes a conserved proline-rich protein predominant in kidney: analysis of genomic organization, expression, and mutation status in breast and colorectal carcinomas.
2003
2003
Perinatal findings and molecular cytogenetic analysis of trisomy 16q and 22q13.3 deletion
To present the perinatal findings and molecular cytogenetic analysis of a case with concomitant trisomy 16q and 22q13.3 deletion… 
1981
1981
Conserved autosomal syntenic group on mouse (MMU) chromosome 15 and human (HSA) chromosome 22: assignment of a gene for arylsulfatase A to MMU 15 and regional mapping of DIA1, ARSA, and ACO2 on HSA…
We have utilized a panel of Chinese hamster x mouse somatic cell hybrids segregating mouse chromosomes to assign a gene for… 
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