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15q11.2

A chromosome band present on 15q.
National Institutes of Health

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15qChromosomesNIPA1 wt Allele

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2017
2017
Developmental Trajectories for a Sibling Pair with Chromosome 15q11.2-13.1 Duplication Syndrome and Angelman Syndrome
Several types of copy number variants, or a surplus or absence of genetic information encoded by DNA, appear in the 11.2-13.1… 
2016
2016
Cognitive Assessment of 15 q 11 . 2 Deletion Carriers Reveals Domain Specific Impairments
2014
2014
Familial 15q11.2 Micro deletions are not Fully Penetrant in Two Cases with Hereditary Spastic Paraplegia and Dysmorphic Features
Hereditary Spastic Paraplegias (HSP) is heterogenic neurodegenerative disorders with progressive spasticity of the lower limbs as… 
2014
2014
Spread of X inactivation on chromosome 15 is associated with a more severe phenotype in a girl with an unbalanced t(X; 15) translocation
We report on a baby girl with multiple congenital abnormalities, including cleft palate, intrauterine growth restriction, and… 
2009
2009
Mesangioproliferative glomerulonephritis in an infant with Prader-Willi syndrome.
Prader-Willi syndrome (PWS) is a neurobehavioral disorder characterized mainly by neonatal hypotonia, dysmorphic features… 
2007
2007
Genome Wide-DNA Profiling of HIV-Related Non-Hodgkin Lymphomas: Implications for Disease Pathogenesis and Histogenesis.
Non-Hodgkin’s lymphomas (NHL) represent a frequent complication of HIV infection and a major source of morbidity and mortality… 
2001
2001
Klinik und Genetik des Prader-Willi-Syndroms
Fazit: Summary: 
1998
1998
108 Chromosomal Microarray Analysis and the Detection of a 15q11.2 Deletion in a Patient with Hypomelanosis of Ito
Hypomelanosis of Ito (HI) encompasses a group of disorders characterized by hypopigmented whorls, streaks, and patches along… 
1988
1988
A molecular deletion study with Southern hybridization on typical Prader-Willi syndrome (PWS) patients with various chromosome abnormalities involving 15q11–12 and on an atypical PWS patient with…
SummaryWe previously proposed a phenotype-karyotype correlation in the Prader-Willi syndrome (PWS). In order to confirm this… 
1985
1985
X;14 translocation:an exception to the critical region hypothesis on the human X-chromosome.
We report on a family in which an X;14 translocation has been identified. A phenotypically normal female, carrier of an… 
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