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19q13.32
A chromosome band present on 19q
National Institutes of Health
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7 relations
19q
CGB wt Allele
Chromosomes
FOSB wt Allele
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Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2019
2019
Apolipoprotein E-C1-C4-C2 gene cluster region and inter-individual variation in plasma lipoprotein levels: a comprehensive genetic association study in two ethnic groups
D. Pirim
,
Zaheda H. Radwan
,
+7 authors
M. I. Kamboh
PLoS ONE
2019
Corpus ID: 85528527
The apolipoprotein E-C1-C4-C2 gene cluster at 19q13.32 encodes four amphipathic apolipoproteins. The influence of APOE common…
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2017
2017
Expression surrénalienne du glucose-dependent insulinotropic peptide receptor (GIPR) et microduplications de la région 19q13 dans le syndrome de Cushing dépendant de l’alimentation
A. Lecoq
,
C. Stratakis
,
+19 authors
P. Kamenický
2017
Corpus ID: 80510568
2017
2017
A comprehensive association study of apolipoprotein E-C1-C4-C2 gene cluster variation with plasma lipoprotein traits.
Pirim Dilek
,
Zaheda H. Radwan
,
+9 authors
M. I. Kamboh
Atherosclerosis
2017
Corpus ID: 43340615
2015
2015
High-resolution 400K oligonucleotide array comparative genomic hybridization analysis of neurofibromatosis type 1-associated cutaneous neurofibromas.
A. Asai
,
S. Karnan
,
+8 authors
Y. Hosokawa
Gene
2015
Corpus ID: 38014191
2014
2014
Focused screening of a panel of cancer‐related genetic polymorphisms reveals new susceptibility loci for pediatric acute lymphoblastic leukemia
Sonja Offenmüller
,
Y. Ravindranath
,
+4 authors
O. Zolk
Pediatric Blood & Cancer
2014
Corpus ID: 25196841
A genetic predisposition to acute lymphoblastic leukemia (ALL) in childhood is well established. Currently known risk loci…
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Review
2010
Review
2010
[How to explore ... congenital isolated hypogonadotrophic hypogonadism].
H. Valdés-Socin
,
F. Debray
,
+4 authors
A. Beckers
Revue Medicale de Liege
2010
Corpus ID: 38439549
Congenital Isolated hypogonadotropic hypogonadism (CIHH) is caused by an inherited mechanism of impairment of the pituitary…
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2009
2009
Covert preleukemia driven by MLL gene fusion
J. Zuna
,
T. Burjanivová
,
+12 authors
J. Trka
Genes, Chromosomes and Cancer
2009
Corpus ID: 27982659
Acute leukemia is considered to be a two‐ or multiple‐step process. Although there is a considerable knowledge regarding the…
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2009
2009
Array-CGH detection of a de novo 0.8Mb deletion in 19q13.32 associated with mental retardation, cardiac malformation, cleft lip and palate, hearing loss and multiple dysmorphic features.
T. Leal
,
J. Andrieux
,
B. Duban‐Bedu
,
S. Bouquillon
,
G. Brévière
,
B. Delobel
European Journal of Medical Genetics
2009
Corpus ID: 23170056
2004
2004
Infantile bilateral striatal necrosis maps to chromosome 19q
L. Basel‐Vanagaite
,
R. Straussberg
,
+6 authors
M. Shohat
Neurology
2004
Corpus ID: 3144970
Background: Infantile bilateral striatal necrosis (IBSN) encompasses several syndromes of bilateral symmetric degeneration of the…
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2004
2004
GENETIC SUSCEPTIBILITY TO THE METABOLIC SYNDROME
Y. Bossé
2004
Corpus ID: 87514400
The metabolic syndrome is a cluster of interrelated cardiovascular risk factors co-occurring in the same individual. People with…
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