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Chromosome 15q, trisomy
Known as:
Duplication 15q
, Trisomy 15q
National Institutes of Health
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Related topics
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2 relations
Broader (2)
Chromosomes, Human, Pair 15
Trisomy
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2018
2018
Significant transcriptional changes in 15q duplication but not Angelman syndrome deletion stem cell-derived neurons
N. Urraca
,
Kevin A. Hope
,
+10 authors
L. Reiter
Molecular Autism
2018
Corpus ID: 21819209
BackgroundThe inability to analyze gene expression in living neurons from Angelman (AS) and Duplication 15q (Dup15q) syndrome…
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2017
2017
Partial monosomy of 10p and duplication of another chromosome in two patients
Sayaka Ohta
,
T. Isojima
,
+8 authors
A. Oka
Pediatrics International
2017
Corpus ID: 34137812
Partial monosomy of 10p is a rare chromosomal abnormality. Common features are hypoparathyroidism, deafness, renal anomalies…
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2011
2011
Siblings with deletion 22q13.3 and trisomy 15q26 inherited from a maternally balanced translocation.
P. Su
,
Jia-yuh Chen
,
Suh-Jen Chen
Pediatrics and Neonatology
2011
Corpus ID: 12177569
2011
2011
A case of de novo duplication of 15q24-q26.3
E. Y. Kim
,
Y. Kim
,
+4 authors
J. Sin
Korean Journal of Pediatrics
2011
Corpus ID: 16214853
Distal duplication, or trisomy 15q, is an extremely rare chromosomal disorder characterized by prenatal and postnatal overgrowth…
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2004
2004
Inverted duplication of 15q with terminal deletion in a multiple malformed newborn with intrauterine growth failure and lethal phenotype.
R. Genesio
,
D. De Brasi
,
+6 authors
L. Nitsch
American Journal of Medical Genetics. Part A
2004
Corpus ID: 10297698
We describe the cytogenetic and molecular characterization of an inverted duplication of chromosome 15q with evidence of a…
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2002
2002
Optic disc Drusen associated with trisomy 15q.
Martina Wollenhaupt
,
E. Palmer
,
E. Magenis
,
R. Egan
Journal of AAPOS
2002
Corpus ID: 33734664
Review
1997
Review
1997
Partial trisomy 15q: report of a patient and literature review.
K. Chandler
,
C. Schrander‐Stumpel
,
J. Engelen
,
P. Theunissen
,
J. Fryns
Genetic Counseling
1997
Corpus ID: 29456857
We report a girl with severe developmental delay, scoliosis and mild dysmorphism. She was found to have a partial duplication of…
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