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19q13.42

A chromosome band present on 19q
National Institutes of Health

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7 relations
19qChromosomesEPS8L1 wt AlleleMIR518E wt Allele

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2018
2018
Genetic predisposition to PEG‐asparaginase hypersensitivity in children treated according to NOPHO ALL2008
Asparaginase is essential in childhood acute lymphoblastic leukaemia (ALL) treatment, however hypersensitivity reactions to… 
Review
2015
Review
2015
Intraocular Medulloepitheliomas and Embryonal Tumors With Multilayered Rosettes of the Brain: Comparative Roles of LIN28A and C19MC.
Highly Cited
2012
Highly Cited
2012
LIN28A immunoreactivity is a potent diagnostic marker of embryonal tumor with multilayered rosettes (ETMR)
Embryonal tumor with multilayered rosettes (ETMR, previously known as ETANTR) is a highly aggressive embryonal CNS tumor, which… 
2012
2012
A novel 7 bp deletion in PRPF31 associated with autosomal dominant retinitis pigmentosa with incomplete penetrance in an Indian family.
Review
2011
Review
2011
Embryonal tumors with abundant neuropil and true rosettes: 2 illustrative cases and a review of the literature.
Embryonal tumor with abundant neuropil and true rosettes (ETANTR) is a recently identified variant of primitive neuroectodermal… 
Highly Cited
2009
Highly Cited
2009
Differential expression profile of microRNAs in human placentas from preeclamptic pregnancies vs normal pregnancies.
2009
2009
Breakpoint characterization of a novel ∼59 kb genomic deletion on 19q13.42 in autosomal-dominant retinitis pigmentosa with incomplete penetrance
The aim of this study was to identify and characterize the underlying molecular mechanisms in autosomal-dominant retinitis… 
Highly Cited
2008
Highly Cited
2008
Novel genomic amplification targeting the microRNA cluster at 19q13.42 in a pediatric embryonal tumor with abundant neuropil and true rosettes
Embryonal tumors with abundant neuropil and true rosettes (ETANTR) comprise a rare variant of embryonal brain tumors usually… 
Highly Cited
2008
Highly Cited
2008
A recurrent intragenic genomic duplication, other novel mutations in NLRP7 and imprinting defects in recurrent biparental hydatidiform moles.
A complete hydatidiform mole (CHM) is an abnormal pregnancy with hyperproliferative vesicular trophoblast and no fetal… 
Highly Cited
2003
Highly Cited
2003
Genome-wide detection of LOH in prostate cancer using human SNP microarray technology.
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