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4p15.32

A chromosome band present on 4p
National Institutes of Health

Papers overview

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Review
2016
Review
2016
Abstract Rhegmatogenous retinal detachment (RRD) is a common and potentially blinding surgical retinal disease. While the precise… 
2014
2014
CD38 encodes a ligand in the oxytocin signaling pathway. Some single nucleotide polymorphisms in this gene have been associated… 
2014
2014
Microtia is a congenital deformity where the external ear is underdeveloped. Genetic investigations have identified many… 
2011
2011
The aim of this study was to obtain a quantitative definition of Wolf–Hirschhorn syndrome (WHS) through systematic phenotypic… 
Review
2008
Review
2008
Wolf–Hirschhorn syndrome (WHS) is a well‐known multiple congenital anomalies/mental retardation syndrome, firstly described in… 
Review
2007
Review
2007
2005
2005
BACKGROUND In an attempt to map the genes predisposing to the common, complex aetiologies of end-stage renal disease (ESRD), we… 
1986
1986
A 7 7/12‐year‐old girl with a de novo deletion 4p15.32→ pter without the typical Wolf‐Hirschhorn syndrome (WHS) is presented…