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4p16.1

A chromosome band present on 4p
National Institutes of Health

Related topics

Related topics

3 relations
Chromosome 4 Short ArmChromosomesDRD5 wt Allele

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
Review
2012
Review
2012
Wolfram syndrome 1 and Wolfram syndrome 2 : clinical implications for pediatricians
Purpose of review Wolfram syndrome 1 (WS1) is an autosomal recessive disorder characterized by diabetes insipidus, diabetes… 
2009
2009
Variability of origin for the neocentromeric sequences in analphoid supernumerary marker chromosomes of well-differentiated liposarcomas.
2004
2004
Possible evidence for a common risk locus for bipolar affective disorder and schizophrenia on chromosome 4p16 in patients from the Faroe Islands
Patients with schizophrenia (n=11) and bipolar affective disorder (n=17) from the relatively isolated population of the Faroe… 
2002
2002
Unstable transmission of the RS447 human megasatellite tandem repetitive sequence that contains the USP17 deubiquitinating enzyme gene
Abstract. The RS447 megasatellite DNA, which maps to human chromosome 4p16.1, is a highly polymorphic conserved tandem repetitive… 
1997
1997
Molecular cloning, chromosomal mapping and developmental expression of BAPX1, a novel human homeobox-containing gene homologous to Drosophila bagpipe.
1997
1997
Sequence and chromosomal assignment of human BAPX1, a bagpipe-related gene, to 4p16.1: a candidate gene for skeletal dysplasia.
Homeobox-containing genes play an important role in both body axis determination and specific organ development. They have… 
Highly Cited
1996
Highly Cited
1996
Linkage of Wolfram syndrome to chromosome 4p16.1 and evidence for heterogeneity.
Wolfram syndrome (DIDMOAD syndrome; MIM 222300) is an autosomal recessive neurodegenerative disorder characterized by juvenile… 
1992
1992
Identification and genetic mapping of a homeobox gene to the 4p16.1 region of human chromosome 4.
A human craniofacial cDNA library was screened with a degenerate oligonucleotide probe based on the conserved third helix of… 
1988
1988
A polymorphic DNA marker that represents a conserved expressed sequence in the region of the Huntington disease gene.
A polymorphic marker (D4S62) that is genetically closely linked to D4S10 and is in the region of the gene for Huntington disease… 
1986
1986
Subregional assignment of the linked marker G8 (D4S10) for Huntington disease to chromosome 4p16.1-16.3.
The linked DNA marker for Huntington disease has recently been mapped to the short arm of chromosome 4 by somatic cell… 
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