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rdf:type |
|
|
lifeskim:mentions |
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pubmed:issue |
3
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pubmed:dateCreated |
2006-3-6
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|
pubmed:abstractText |
We report a case of prenatal diagnosis of trisomy 20p resulting from a maternal pericentric inversion. The diagnosis was confirmed on both chorionic villi and amniotic cells. This case underlines the fact that prenatal ultrasound diagnosis of this structural anomaly is difficult. The only early sonographic feature was increased nuchal translucency.
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pubmed:language |
eng
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pubmed:journal |
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|
pubmed:citationSubset |
IM
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|
pubmed:status |
MEDLINE
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|
pubmed:month |
Mar
|
|
pubmed:issn |
0197-3851
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pubmed:author |
|
|
pubmed:copyrightInfo |
2006 John Wiley & Sons, Ltd.
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pubmed:issnType |
Print
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pubmed:volume |
26
|
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pubmed:owner |
NLM
|
|
pubmed:authorsComplete |
Y
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pubmed:pagination |
239-41
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pubmed:dateRevised |
2009-11-19
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|
pubmed:meshHeading |
pubmed-meshheading:16485319-Adult,
pubmed-meshheading:16485319-Chorionic Villi Sampling,
pubmed-meshheading:16485319-Chromosome Inversion,
pubmed-meshheading:16485319-Chromosomes, Human, Pair 20,
pubmed-meshheading:16485319-Female,
pubmed-meshheading:16485319-Fetal Diseases,
pubmed-meshheading:16485319-Humans,
pubmed-meshheading:16485319-Male,
pubmed-meshheading:16485319-Nuchal Translucency Measurement,
pubmed-meshheading:16485319-Pregnancy,
pubmed-meshheading:16485319-Trisomy
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|
pubmed:year |
2006
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|
pubmed:articleTitle |
Partial trisomy 20p resulting from recombination of a maternal pericentric inversion: case report of a prenatal diagnosis by chorionic villus sampling.
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pubmed:affiliation |
Department of Cytogenetics, CHI Poissy-St Germain-en-Laye, Poissy, France.
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pubmed:publicationType |
Journal Article,
Case Reports
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