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19q13.42
A chromosome band present on 19q
National Institutes of Health
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Related topics
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7 relations
19q
Chromosomes
EPS8L1 wt Allele
MIR518E wt Allele
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Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2018
2018
Genomic duplication in the 19q13.42 imprinted region identified as a new genetic cause of intrauterine growth restriction
Graciane Pètre
,
P. Lorès
,
+16 authors
M. Bidart
Clinical Genetics
2018
Corpus ID: 52281467
We report findings from a male fetus of 26 weeks' gestational age with severe isolated intrauterine growth restriction (IUGR…
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2015
2015
[Clinicopathologic features of embryonal tumor with multilayered rosettes and gene analysis on chromosome 19q13.42].
Junmei Wang
,
Zhao-xia Liu
,
+4 authors
Guilin Li
Zhonghua bing li xue za zhi = Chinese journal of…
2015
Corpus ID: 37644394
OBJECTIVE To investigate the clinicopathologic features and 19q13.42 gene changes in embryonal tumors with multilayered rosettes…
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2014
2014
Gene-Based Rare Allele Analysis Identified a Risk Gene of Alzheimer’s Disease
Jong Hun Kim
,
Pamela Song
,
H. Lim
,
Jae-Hyung Lee
,
Jun Hong Lee
,
S. A. Park
PLoS ONE
2014
Corpus ID: 9941180
Alzheimer’s disease (AD) has a strong propensity to run in families. However, the known risk genes excluding APOE are not…
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2014
2014
Embryonal tumor with abundant neuropil and true rosettes with only one structure suggestive of an ependymoblastic rosette
S. Nobusawa
,
Kenta Orimo
,
+4 authors
Y. Nakazato
Pathology international (Print)
2014
Corpus ID: 643069
Embryonal tumor with abundant neuropil and true rosettes (ETANTR) is a very aggressive embryonal central nervous system (CNS…
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2013
2013
Anaplastic ependymoma with ependymoblastic multilayered rosettes.
S. Nobusawa
,
A. Suzuki
,
+5 authors
Y. Nakazato
Human Pathology
2013
Corpus ID: 25879299
2013
2013
Two novel PRPF31 premessenger ribonucleic acid processing factor 31 homolog mutations including a complex insertion-deletion identified in Chinese families with retinitis pigmentosa
B. Dong
,
Jieqiong Chen
,
Xiao-hui Zhang
,
Zhe Pan
,
F. Bai
,
Yang Li
Molecular Vision
2013
Corpus ID: 17174805
Objective To identify the causative mutations in two Chinese families with retinitis pigmentosa (RP), and to describe the…
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Review
2013
Review
2013
Shared genetic factors for age at natural menopause in Iranian and European women.
M. Rahmani
,
M. Earp
,
+9 authors
A. Brooks-Wilson
Human Reproduction
2013
Corpus ID: 8689617
STUDY QUESTION Do differences in heritable genetic factors explain some of the difference in age at natural menopause (ANM) among…
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2012
2012
A novel 7 bp deletion in PRPF31 associated with autosomal dominant retinitis pigmentosa with incomplete penetrance in an Indian family.
S. Saini
,
P. Robinson
,
J. Singh
,
V. Vanita
Experimental Eye Research
2012
Corpus ID: 41556105
2011
2011
Embryonal tumor with abundant neuropil and true rosettes (ETANTR) with a focal amplification at chromosome 19q13.42 locus: Further evidence of two new instances in China
Yin Wang
,
Shu-guang Chu
,
J. Xiong
,
Haixia Cheng
,
Hong Chen
,
Xiao-hong Yao
Neuropathology (Kyoto. )
2011
Corpus ID: 205472482
Recently, the term “embryonal tumor with multilayered rosettes” (ETMR), including embryonal tumor with abundant neuropil and true…
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Review
2011
Review
2011
Multinodular leptomeningeal metastases from ETANTR contain both small blue cell and maturing neuropil elements
B. Kleinschmidt-DeMasters
,
A. Boylan
,
K. Capocelli
,
P. Boyer
,
N. Foreman
Acta Neuropathologica
2011
Corpus ID: 1285866
Embryonal tumor with abundant neuropil and true rosettes (ETANTR), a rare, malignant neoplasm of infancy occurring in the…
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