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4p15.32

A chromosome band present on 4p
National Institutes of Health

Papers overview

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2015
2015
Neurofibromatosis type 1 (NF1) is a genetic disorder where affected individuals develop benign or malignant nervous system tumors… Expand
2015
2015
ABCA4 ATP-binding cassette, sub-family A (ABC1), member 4 1p21-23 ADAM9 A disintegrin and metalloproteinase domain 9 8p11.23… Expand
2014
2014
CD38 encodes a ligand in the oxytocin signaling pathway. Some single nucleotide polymorphisms in this gene have been associated… Expand
2014
2014
Microtia is a congenital deformity where the external ear is underdeveloped. Genetic investigations have identified many… Expand
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2011
2011
The aim of this study was to obtain a quantitative definition of Wolf–Hirschhorn syndrome (WHS) through systematic phenotypic… Expand
Review
2007
Review
2007
Prominin-1 (alias CD133, PROML1; NCBI accession number: NM_006017, human; NM_008935, mouse; NM_021751, rat) is a membrane… Expand
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2005
2005
BACKGROUND In an attempt to map the genes predisposing to the common, complex aetiologies of end-stage renal disease (ESRD), we… Expand
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1998
1998
Abstract Mutations in ion channels have been shown to be responsible for a variety of neurological and muscular diseases. The… Expand
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1991
1991
Treacher Collins syndrome is an autosomal dominant condition of bilateral craniofacial abnormalities of structures derived from… Expand
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… Expand