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16q24.3

A chromosome band present on 16q
National Institutes of Health

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11 relations
16qCDT1 wt AlleleCPNE7 wt AlleleChromosomes

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2013
2013
Haploinsufficiency of ANKRD11 (16q24.3) Is Not Obligatorily Associated with Cognitive Impairment but Shows a Clinical Overlap with Silver-Russell Syndrome
Microdeletions in 16q24.3 are associated with intellectual disability and a specific phenotype, e.g. short stature and a… 
2012
2012
Microcephaly, intellectual impairment, bilateral vesicoureteral reflux, distichiasis, and glomuvenous malformations associated with a 16q24.3 contiguous gene deletion and a Glomulin mutation
Two hereditary syndromes, lymphedema‐distichiasis (LD) syndrome and blepharo‐chelio‐dontic (BCD) syndrome include the aberrant… 
2009
2009
Linkage analysis of schizophrenia in African-American families
2008
2008
Complicated autosomal recessive hereditary spastic paraplegia
Hereditary spastic paraplegia (HSP) has emerged as one of the most genetically heterogeneous neurodegenerative disorders. Almost… 
Review
2003
Review
2003
Huntington's disease-like 2: a clinical, pathological, and molecular comparison to Huntington's disease
2001
2001
Alterations of the 16q22.1 and 16q24.3 chromosomal loci in sporadic invasive breast carcinomas: correlation with proliferative activity, ploidy and hormonal status of the tumors.
BACKGROUND Breast cancer is characterized by complex genetic alterations found in multiple chromosomal regions, most commonly… 
Highly Cited
2000
Highly Cited
2000
Loss of heterozygosity at chromosomes 3, 6, 8, 11, 16, and 17 in ovarian cancer: correlation to clinicopathological variables.
1999
1999
Identification of a gene at 16q24.3 that restores cellular senescence in immortal mammary tumor cells
We have mapped a cellular senescence gene, SEN16, within a genetic distance of 3 – 7 cM, at 16q24.3. Microcell mediated transfer… 
1999
1999
The PISSLRE gene: structure, exon skipping, and exclusion as tumor suppressor in breast cancer.
In sporadic breast cancer, loss of heterozygosity (LOH) frequently occurs in three discrete regions of the long arm of chromosome… 
1995
1995
Mapping of the breast basic conserved gene (D16S444E) to human chromosome band 16q24.3.
The breast basic conserved gene (D16S444E) is a candidate tumor suppressor gene previously mapped to human chromosome 16. We… 
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