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16q12.1

A chromosome band present on 16q
National Institutes of Health

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6 relations
16qCYLD wt AlleleChromosomesGPT2 wt Allele

Papers overview

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2019
2019
Two novel genes TOX3 and COL21A1 in large extended Malay families with nonsyndromic cleft lip and/or palate
Nonsyndromic cleft lip and/or palate is one of the most common human birth defects worldwide that affects the lip and/or palate… 
2016
2016
Discovery of candidate genes for nonsyndromic cleft lip palate through genome-wide linkage analysis of large extended families in the Malay population
Nonsyndromic orofacial clefts are one of the most common birth defects worldwide. It occurs as a result of genetic or… 
2011
2011
Correction: Genome-Wide Association Study Identifies Novel Restless Legs Syndrome Susceptibility Loci on 2p14 and 16q12.1
An affiliation and its funding information were omitted from the published paper. Siong-Chi Lin and Zbigniew Wszolek are also… 
2008
2008
A BFIS‐like syndrome with late onset and febrile seizures: Suggestive linkage to chromosome 16p11.2–16q12.1
Benign familial infantile seizures (BFIS) is a dominant idiopathic epilepsy with partial and secondarily generalized seizures… 
2005
2005
Small reciprocal insertion detected by spectral karyotyping (SKY) and delimited by array-CGH analysis.
2003
2003
Characterization of the mouse Abcc12 gene and its transcript encoding an ATP-binding cassette transporter, an orthologue of human ABCC12.
2002
2002
Mapping of the wet/dry earwax locus to the pericentromeric region of chromosome 16
2000
2000
Molecular cloning, chromosomal localization, and expression of the murine SALL1 ortholog Sall1
SALL1 has been identified as one of now three human homologs of the region specific homeotic gene spalt (sal) of Drosophila… 
1997
1997
Variant euchromatic band within 16q12.1
The enlarged short arm of chromosome 16 resulting in an additional euchromatic band has been regarded as a variant. We present an… 
Highly Cited
1995
Highly Cited
1995
Frequent microsatellite alterations on chromosome 3p in esophageal squamous cell carcinoma.
By the microsatellite assay, two types of genetic alterations, loss of heterozygosity (LOH) and replication error (RER), were… 
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