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Chromosome 6 Short Arm

Known as: 6p, Chromosome 6 Proximal Arm 
Proximal (short) arm of chromosome 6
National Institutes of Health

Related topics

Related topics

27 relations
6p11.16p11.26p126p12.1

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
Review
2003
Review
2003
Obesity – is it a genetic disorder?
Abstract.  Loos RJF, Bouchard C (Human Genomics Laboratory, Pennington Biomedical Research Center, Baton Rouge, LA, USA). Obesity… 
Highly Cited
2002
Highly Cited
2002
A genome-wide scan for linkage to chromosomal regions in 382 sibling pairs with schizophrenia or schizoaffective disorder.
OBJECTIVE Some genome-wide scans and association studies for schizophrenia susceptibility genes have yielded significant positive… 
Highly Cited
2001
Highly Cited
2001
Whole-genome screening in ankylosing spondylitis: evidence of non-MHC genetic-susceptibility loci.
Ankylosing spondylitis (AS) is a common inflammatory arthritis predominantly affecting the axial skeleton. Susceptibility to the… 
Highly Cited
2000
Highly Cited
2000
The gene TFR2 is mutated in a new type of haemochromatosis mapping to 7q22
Haemochromatosis is a common recessive disorder characterized by progressive iron overload, which may lead to severe clinical… 
Highly Cited
2000
Highly Cited
2000
An optimized set of human telomere clones for studying telomere integrity and architecture.
Telomere-specific clones are a valuable resource for the characterization of chromosomal rearrangements. We previously reported a… 
Highly Cited
1998
Highly Cited
1998
The forkhead transcription factor gene FKHL7 is responsible for glaucoma phenotypes which map to 6p25
A number of different eye disorders with the presence of early-onset glaucoma as a component of the phenotype have been mapped to… 
Highly Cited
1997
Highly Cited
1997
Screening of germline mutations in the CDKN2A and CDKN2B genes in Swedish families with hereditary cutaneous melanoma.
BACKGROUND Approximately 10% of human cutaneous melanomas occur in families in which several members are affected. The familial… 
Highly Cited
1994
Highly Cited
1994
Quantitative trait locus for reading disability on chromosome 6.
Interval mapping of data from two independent samples of sib pairs, at least one member of whom was reading disabled, revealed… 
Highly Cited
1993
Highly Cited
1993
Human epithelial ovarian cancer allelotype.
To determine which chromosomes and chromosomal regions contain putative tumor suppressor genes important for human epithelial… 
Review
1990
Review
1990
Uterine leiomyoma cytogenetics
Uterine leiomyoma—a benign smooth muscle tumor—has recently been found to contain tumor‐specific chromosome aberrations. Although… 
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