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4p15.32

A chromosome band present on 4p
National Institutes of Health

Related topics

Related topics

3 relations
Chromosome 4 Short ArmChromosomesPROM1 wt Allele

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2017
2017
Genome-Wide Gene–Potassium Interaction Analyses on Blood Pressure: The GenSalt Study (Genetic Epidemiology Network of Salt Sensitivity)
Background— Gene–environmental interaction analysis can identify novel genetic factors for blood pressure (BP). We performed… 
2015
2015
High-resolution 400K oligonucleotide array comparative genomic hybridization analysis of neurofibromatosis type 1-associated cutaneous neurofibromas.
2015
2015
Clinical Utility Gene Card for: autosomal recessive cone-rod dystrophy
ABCA4 ATP-binding cassette, sub-family A (ABC1), member 4 1p21-23 ADAM9 A disintegrin and metalloproteinase domain 9 8p11.23… 
2014
2014
Genome-Wide Linkage Study Suggests a Susceptibility Locus for Isolated Bilateral Microtia on 4p15.32–4p16.2
Microtia is a congenital deformity where the external ear is underdeveloped. Genetic investigations have identified many… 
2011
2011
Wolf–Hirschhorn syndrome due to pure and translocation forms of monosomy 4p16.1 → pter
The aim of this study was to obtain a quantitative definition of Wolf–Hirschhorn syndrome (WHS) through systematic phenotypic… 
Review
2007
Review
2007
Focus on molecules: prominin-1 (CD133).
1998
1998
Refined localisation of the voltage-gated chloride channel, CLCN3, to 4q33
Abstract Mutations in ion channels have been shown to be responsible for a variety of neurological and muscular diseases. The… 
1991
1991
Chromosomal deletion 4p15.32----p14 in a Treacher Collins syndrome patient: exclusion of the disease locus from and mapping of anonymous DNA sequences to this region.
1990
1990
Probable assignment of the dihydropteridine reductase gene to 4p15.31.
We report the dihydropteridine reductase (DHPR) activity in cases with interstitial deletion of the short arm of chromosome 4… 
1986
1986
De novo del(4) (p15.32) with incomplete expression of the Wolf‐Hirschhorn syndrome
A 7 7/12‐year‐old girl with a de novo deletion 4p15.32→ pter without the typical Wolf‐Hirschhorn syndrome (WHS) is presented… 
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