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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.
2019
2019
Magnesium Supplement and the 15q11.2 BP1–BP2 Microdeletion (Burnside–Butler) Syndrome: A Potential Treatment?
The 15q11.2 BP1–BP2 microdeletion (Burnside–Butler) syndrome is an emerging disorder that encompasses four genes (NIPA1, NIPA2… 
2016
2016
Prenatal Array Comparative Genomic Hybridization in Fetuses With Structural Cardiac Anomalies.
2014
2014
Congenital Arthrogryposis: An Extension of the 15q11.2 BP1-BP2 Microdeletion Syndrome?
The proximal 15q11–q13 region contains 5 breakpoints (BP1–BP5). The BP1-BP2 region spans approximately 500 kb and contains four… 
2013
2013
Integrative analysis of copy number alteration and gene expression profiling in ovarian clear cell adenocarcinoma.
2011
2011
NIPA1 mutation in complex hereditary spastic paraplegia with epilepsy
Background and purpose:  Hereditary spastic paraplegia (HSP) is a group of clinically and genetically heterogeneous… 
2007
2007
High-resolution melting for accurate assessment of DNA methylation.
Methylation of cytosine in DNA is an epigenetic mark that is important for genome stability, transcriptional regulation of… 
1990
1990
Cytogenetic and molecular study of Angelman syndrome.
Six patients, including two sibs, with Angelman syndrome (AS; three females and three males, aged 11 to 18 years) were studied… 
1988
1988
A cytogenetic and molecular analysis of five variant Philadelphia translocations in chronic myeloid leukemia.
1988
1988
Similar molecular deletions on chromosome 15q11.2 are encountered in both the Prader-Willi and Angelman syndromes
SummaryComparative molecular analysis of chromosome 15, sub-band q11.2 of patients with the Prader-Willi or Angelman syndromes… 
1984
1984
A case of an interstitial deletion of the long arm of chromosome 5: 46,XX,del(5)(q15q22)
SummaryA female infant with mild mental retardation and dysmorphic features was found to have an interstitial deletion of the… 
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