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19p13.12
A chromosome band present on 19p
National Institutes of Health
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Related topics
Related topics
5 relations
Chromosome 19 Short Arm
Chromosomes
MED26 wt Allele
MIR27A wt Allele
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Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2018
2018
First prenatal case of proximal 19p13.12 microdeletion syndrome: New insights and new delineation of the syndrome.
Minh-Tuan Huynh
,
L. Tosca
,
+11 authors
S. Brisset
European Journal of Medical Genetics
2018
Corpus ID: 24110657
2015
2015
Clinical and molecular characterization of an infant with a tandem duplication and deletion of 19p13
R. Tan
,
R. Witlox
,
+8 authors
G. Santen
American Journal of Medical Genetics. Part A
2015
Corpus ID: 42959332
Copy number variations (CNVs) on the short arm of chromosome 19 are relatively rare. We present a patient with a tandem de novo 3…
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2014
2014
22q11.2 Microduplication in a patient with 19p13.12-13.13 deletion.
Ying Wang
,
Yongguo Yu
,
Xiao-wei Hu
,
Bi-ru Li
,
J. Qian
Gene
2014
Corpus ID: 205018865
2014
2014
A genome scan for Plasmodium falciparum malaria identifies quantitative trait loci on chromosomes 5q31, 6p21.3, 17p12, and 19p13
A. Brisebarre
,
B. Kumulungui
,
+4 authors
P. Rihet
Malaria Journal
2014
Corpus ID: 255860310
Genome-wide studies have mapped several loci controlling Plasmodium falciparum mild malaria and parasitaemia, only two of them…
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2013
2013
Genome scan in familial late‐onset Alzheimer's disease: A locus on chromosome 6 contributes to age‐at‐onset
Wei Zhao
,
E. Marchani
,
+4 authors
E. Wijsman
American Journal of Medical Genetics Part B…
2013
Corpus ID: 34908172
Alzheimer's disease (AD) is a common, genetically complex, fatal neurodegenerative disorder of late life. Although several genes…
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2011
2011
Branchial arch defects and 19p13.12 microdeletion: Defining the critical region into a 0.8 M base interval
K. Kosaki
,
H. Saito
,
R. Kosaki
,
C. Torii
,
K. Kishi
,
Takao Takahashi
American Journal of Medical Genetics. Part A
2011
Corpus ID: 205314192
We present a patient with preauricular tags, preauricular and branchial pits, stenosis of the external auditory canals, mild…
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2011
2011
Pontocerebellar hypoplasia in association with de novo 19p13.11p13.12 microdeletion
N. Gallant
,
E. Baldwin
,
N. Salamon
,
K. Dipple
,
F. Quintero-Rivera
American Journal of Medical Genetics. Part A
2011
Corpus ID: 28111981
The pontocerebellar hypoplasias (PCHs) are a group of clinically variable disorders characterized by abnormally small cerebellum…
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2010
2010
A boy with mental retardation, obesity and hypertrichosis caused by a microdeletion of 19p13.12.
N. van der Aa
,
G. Vandeweyer
,
R. Kooy
European Journal of Medical Genetics
2010
Corpus ID: 10604693
2009
2009
A novel chromosome 19p13.12 deletion in a child with multiple congenital anomalies
Daniel R. Jensen
,
D. M. Martin
,
+8 authors
M. Lesperance
American Journal of Medical Genetics. Part A
2009
Corpus ID: 15779017
We describe a patient with multiple congenital anomalies including deafness, lacrimal duct stenosis, strabismus, bilateral…
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1997
1997
Chromosome mapping of the Emr1 gene
A. Mcknight
,
A. Macfarlane
,
M. Seldin
,
S. Gordon
Mammalian Genome
1997
Corpus ID: 28566053
Species: Mouse Locus name: EGF-module-containing mucin-like hormone receptor 1 Locus symbol: Emrl Map position: The distal region…
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