15q11-q13

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

Papers overview

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2009
2009
BACKGROUND Maternally derived duplications of the 15q11-q13 region are the most frequently reported chromosomal aberrations in… (More)
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Highly Cited
2004
Highly Cited
2004
Maternally derived duplication of the imprinted region of chromosome 15q11-q14 leads to a complex neurobehavioral phenotype that… (More)
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2004
2004
Chromosome 15q11-q13 is one of the most variable regions of the human genome, with numerous clinical rearrangements involving a… (More)
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Highly Cited
2003
Highly Cited
2003
Autistic disorder (AutD) is a complex genetic disease. Available evidence suggests that several genes contribute to the… (More)
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Highly Cited
2003
Highly Cited
2003
Parental submicroscopic genomic inversions have recently been demonstrated to be present in several genomic disorders. These… (More)
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2003
2003
OBJECTIVE Autism displays a remarkably high heritability but a complex genetic etiology. One approach to identifying… (More)
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Review
2001
Review
2001
The chromosomal region, 15q11-q13, involved in Prader-Willi and Angelman syndromes (PWS and AS) represents a paradigm for… (More)
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Highly Cited
1999
Highly Cited
1999
The most common etiology for Prader-Willi syndrome and Angelman syndrome is de novo interstitial deletion of chromosome 15q11-q13… (More)
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1994
1994
A 7 year old girl with intrachromosomal triplication 46,XX,-15,+der(15)(pter-->q13::q13-->q11::q11-->qter) resulting in tetrasomy… (More)
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1993
1993
The clearest example of genomic imprinting in humans comes from studies of the Angelman (AS) and Prader-Willi (PWS) syndromes… (More)
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