11746139

Source:http://linkedlifedata.com/resource/pubmed/id/11746139

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0015780, umls-concept:C0021270, umls-concept:C0033053, umls-concept:C0041427, umls-concept:C1261273, umls-concept:C1882365
pubmed:issue	10
pubmed:dateCreated	2001-12-17
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/8106540
pubmed:citationSubset	IM
pubmed:status	MEDLINE
pubmed:month	Oct
pubmed:issn	0197-3851
pubmed:author	pubmed-author:LecumberriJ MJM, pubmed-author:LloverasEE, pubmed-author:MeleroCC, pubmed-author:PérezCC, pubmed-author:PlajaAA, pubmed-author:SánchezM AMA, pubmed-author:SoléFF, pubmed-author:ZamoraLL
pubmed:issnType	Print
pubmed:volume	21
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	896-7
pubmed:dateRevised	2004-11-17
pubmed:meshHeading	pubmed-meshheading:11746139-Diseases in Twins, pubmed-meshheading:11746139-Female, pubmed-meshheading:11746139-Fetal Resorption, pubmed-meshheading:11746139-Humans, pubmed-meshheading:11746139-Karyotyping, pubmed-meshheading:11746139-Male, pubmed-meshheading:11746139-Pregnancy, pubmed-meshheading:11746139-Prenatal Diagnosis
pubmed:year	2001
pubmed:articleTitle	A female infant with a 46,XX/48,XY, +8, +10 karyotype in prenatal diagnosis: a 'vanishing twin' phenomenon?
pubmed:publicationType	Letter, Case Reports