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16q22

A chromosome band present on 16q
National Institutes of Health

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6 relations
16qAGRP wt AlleleCBFB wt AlleleChromosomes

Papers overview

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2011
2011
The "missing" link in atrial fibrillation heritability.
Highly Cited
2006
Highly Cited
2006
Expression of cadherins and catenins correlates with distinct histologic types of ovarian carcinomas.
Highly Cited
2005
Highly Cited
2005
Locus heterogeneity in autosomal recessive congenital cataracts: linkage to 9q and germline HSF4 mutations
Isolated (non-syndromic) congenital cataract may be inherited as an autosomal dominant, autosomal recessive, or X-linked… 
Highly Cited
2004
Highly Cited
2004
A homozygous splice mutation in the HSF4 gene is associated with an autosomal recessive congenital cataract.
PURPOSE To map the locus and identify the gene causing autosomal recessive congenital cataracts in a large consanguineous… 
2003
2003
Chromosomal gains and losses in ocular melanoma detected by comparative genomic hybridization in an Australian population-based study.
1995
1995
Enhanced expression of common fragile site with occupational exposure to pesticides.
1988
1988
Fine mapping of gene probes and anonymous DNA fragments to the long arm of chromosome 16.
Highly Cited
1987
Highly Cited
1987
Fragile sites at 16q22 are not at the breakpoint of the chromosomal rearrangement in AMMoL.
There is much speculation about fragile sites on human chromosomes predisposing to specific chromosome rearrangements seen in… 
Highly Cited
1984
Highly Cited
1984
Recurrent chromosomal defects are found in most patients with acute nonlymphocytic leukemia.
Highly Cited
1984
Highly Cited
1984
Heritable fragile sites on human chromosomes. XI. Factors affecting expression of fragile sites at 10q25, 16q22, and 17p12.
The fragile sites at 10q25, 16q22, and 17p12 can all be induced in lymphocyte culture by BrdU or BrdC added 6-12 hrs prior to… 
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