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trisomy 15

Known as: 15 trisomies 
A chromosomal abnormality consisting of the presence of a third copy of chromosome 15 in somatic cells.
National Institutes of Health

Papers overview

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Highly Cited
2001
Highly Cited
2001
OBJECTIVE To characterize rates of chromosome aneuploidy in sperm from three siblings, one of whom had an IVF/ICSI conceptus with… Expand
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Review
1998
Review
1998
Trisomy 15 as a single autosomal abnormality is a rare finding in hematological disorders and has not as yet been associated with… Expand
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1997
1997
Chronic eosinophilic leukaemia has not yet been clearly defined, mainly due to the fact that it has not been conclusively shown… Expand
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1997
1997
A 3.3 year old girl with Prader-Willi syndrome (PWS) and mosaicism for two aneuploidies, 47,XXX and 47,XX,+15, is presented. The… Expand
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Highly Cited
1996
Highly Cited
1996
Maternal uniparental disomy 15 (UPD15), responsible for approximately 25 per cent of Prader–Willi syndrome cases, is usually… Expand
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Highly Cited
1996
Highly Cited
1996
Prader–Willi syndrome (PWS) results primarily from either a paternal deletion of 15q11–q13 or maternal uniparental disomy (UPD… Expand
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Highly Cited
1992
Highly Cited
1992
Uniparental disomy has recently been recognized to cause human disorders, including Prader-Willi syndrome (PWS). We describe a… Expand
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Highly Cited
1979
Highly Cited
1979
  • G. Klein
  • Proceedings of the National Academy of Sciences…
  • 1979
  • Corpus ID: 11425019
Human B cell lymphoma and murine T cell leukemia can be initiated by several agents. The present paper formulates some thoughts… Expand
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Highly Cited
1978
Highly Cited
1978
The banding pattern of DMBA‐induced leukemias in C57BL/6 mice revealed a very constant chromosome pattern: the presence of… Expand
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1975
1975
A four year old girl with severe mental retardation and multiple congenital abnormalities manifested "partial trisomy 15". Her… Expand
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