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Chromosome 16 Short Arm

Known as: 16p, Chromosome 16 Proximal Arm 
Proximal (short) arm of chromosome 16
National Institutes of Health

Related topics

Related topics

14 relations
16p1116p11.216p11.2-12.116p11.2-p11.1

Papers overview

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2006
2006
Meta-analysis of genome-wide linkage studies for bone mineral density
AbstractGenome-wide linkage studies have shown several chromosome loci that may harbor genes that regulate bone mineral density… 
2002
2002
No association between HOXA1 and HOXB1 genes and autism spectrum disorders (ASD)
Autism (MIM 209850) is an early onset neurodevelopmental disorder with a prevalence rate of at least 5 in 10 000 people1–3 and… 
2001
2001
Identification of extensive genomic loss and gain by comparative genomic hybridisation in malignant astrocytoma in children and young adults
Although astrocytomas are the most common central nervous system tumours in all age groups, there is substantial evidence that… 
Review
1999
Review
1999
Amplification of a pseudogene cassette underlies euchromatic variation of 16p at the cytogenetic level
Abstract Euchromatic imbalances at the cytogenetic level are usually associated with phenotypic consequences. Among the… 
Highly Cited
1998
Highly Cited
1998
Results of a genome-wide genetic screen for panic disorder.
Panic disorder is characterized by spontaneous and recurrent panic attacks, often accompanied by agoraphobia. The results of… 
1997
1997
De novo trisomy 16p.
We report on a patient with psychomotor retardation and a pattern of malformations comprising single umbilical artery… 
1995
1995
Chromosome microdissection identifies cryptic sites of DNA sequence amplification in human ovarian carcinoma.
DNA sequence amplification contributes to the multistep process of carcinogenesis, and overexpression of amplified genes has been… 
1995
1995
Loss of heterozygosity on chromosome arms 5q, 11p, 11q, 13q, and 16p in human testicular germ cell tumors.
To identify common regions of deletion in human testicular germ cell tumors (TGCTs), we have screened tumors from 33 patients for… 
1994
1994
Mapping of two phenol sulphotransferase genes, STP and STM, to 16p: candidate genes for Batten disease.
The cytosolic phenol sulphotransferase gene (STP) was mapped to a region of chromosome 16, within the interval defined by human… 
Review
1992
Review
1992
Trisomy 16p in a liveborn infant and review of trisomy 16p.
We report on an infant boy with duplication of part of 16p and partial deficiency of 9p: 46,XY, -9, + der(9)t(9;16)(p24;p13.1)mat… 
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