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Predicate | Object |
---|---|
rdf:type | |
lifeskim:mentions | |
pubmed:issue |
2
|
pubmed:dateCreated |
1977-4-28
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pubmed:abstractText |
A phenotypically female child, investigated because of short stature, had abnormally large, often bipartite Barr bodies and a mosaicism of 45, X cells and cells with 46 chromosomes which included an exceptionally large metacentric chromosome (Xp+). G- and C-banding established that the chromosome was derived from two substantially entire X chromosomes joined short arm-to-short arm, and was likely to be an isodicentric X with functional inactivation of one centromere.
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pubmed:language |
eng
|
pubmed:journal | |
pubmed:citationSubset |
IM
|
pubmed:status |
MEDLINE
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pubmed:month |
Feb
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pubmed:issn |
0009-9163
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
11
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pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
122-7
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pubmed:dateRevised |
2004-11-17
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pubmed:meshHeading |
pubmed-meshheading:837561-Body Height,
pubmed-meshheading:837561-Body Weight,
pubmed-meshheading:837561-Child,
pubmed-meshheading:837561-Female,
pubmed-meshheading:837561-Humans,
pubmed-meshheading:837561-Karyotyping,
pubmed-meshheading:837561-Mosaicism,
pubmed-meshheading:837561-Sex Chromatin,
pubmed-meshheading:837561-Sex Chromosome Aberrations
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pubmed:year |
1977
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pubmed:articleTitle |
46, X,X-X terminal rearrangement/45, X mosaicism in a child with short stature.
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pubmed:publicationType |
Journal Article,
Case Reports
|