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13q32

A chromosome band present on 13q.
National Institutes of Health

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4 relations
13qABCC4 wt AlleleChromosomesDCT wt Allele

Papers overview

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2015
2015
Holoprosencephaly with cerebellar vermis hypoplasia in 13q deletion syndrome: Critical region for cerebellar dysgenesis within 13q32.2q34
2005
2005
Genetic linkage of systemic lupus erythematosus to 13q32 in African American families with affected male members
Systemic lupus erythematosus (SLE) is a complex autoimmune disorder involving genetic and environmental factors. Previously, our… 
2004
2004
The KPNB3 locus is associated with schizophrenia
2001
2001
Localisation of a novel region of recurrent amplification in follicular lymphoma to an approximately 6.8 Mb region of 13q32-33.
Follicular lymphoma (FL) is characterised by the presence of the t(14;18)(q32;q21) and represents approximately 25% of new cases… 
1999
1999
The candidate tumour suppressor gene, ING1, is retained in colorectal carcinomas.
Highly Cited
1999
Highly Cited
1999
Mapping of novel regions of DNA gain and loss by comparative genomic hybridization in esophageal carcinoma in the Black and Colored populations of South Africa.
Esophageal cancer (EC) is the leading cause of cancer death in the Black male population in South Africa. Although several… 
1999
1999
Neocentromere at 13q32 in one of two stable markers derived from a 13q21 break.
A 10-month-old girl with psychomotor retardation, microcephaly, bilateral microphthalmia, and postaxial polydactyly of the feet… 
1999
1999
On the Future of Genetic Research in Bipolar and Schizophrenic Syndromes
1986
1986
The gene for clotting factor 10 is mapped to 13q32----qter.
The structural gene for the human clotting factor 10 (F10) has been mapped to chromosome 13 with a cDNA probe hybridized to DNAs… 
1973
1973
Nonrandom distribution of chromosome breaks in Fanconi's anemia.
Fanconi’s anemia is characterized by an increased amount of chromosome breaks. The distribution of the breaks in the human… 
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