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rdf:type |
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lifeskim:mentions |
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pubmed:issue |
2
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pubmed:dateCreated |
1999-2-26
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pubmed:abstractText |
To use the molecular identification of Y chromosome material in products of conception cytogenetically diagnosed as "46,XX" to confirm the occurrence of inaccurate cytogenetic test results most likely attributable to maternal cell contamination.
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pubmed:grant |
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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 |
Feb
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pubmed:issn |
0015-0282
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pubmed:author |
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pubmed:issnType |
Print
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pubmed:volume |
71
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
334-41
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pubmed:dateRevised |
2009-11-19
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pubmed:meshHeading |
pubmed-meshheading:9988408-Abortion, Spontaneous,
pubmed-meshheading:9988408-Female,
pubmed-meshheading:9988408-Genetic Testing,
pubmed-meshheading:9988408-Humans,
pubmed-meshheading:9988408-In Situ Hybridization, Fluorescence,
pubmed-meshheading:9988408-Karyotyping,
pubmed-meshheading:9988408-Polymerase Chain Reaction,
pubmed-meshheading:9988408-Predictive Value of Tests,
pubmed-meshheading:9988408-Pregnancy,
pubmed-meshheading:9988408-Pregnancy Trimester, First,
pubmed-meshheading:9988408-Retrospective Studies
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pubmed:year |
1999
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pubmed:articleTitle |
Cytogenetic diagnosis of "normal 46,XX" karyotypes in spontaneous abortions frequently may be misleading.
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pubmed:affiliation |
Department of Pathology and Laboratory Medicine, University of Pennsylvania Medical Center, Philadelphia, USA. kabell@welchlink.welch.jhu.edu
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pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, P.H.S.
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