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rdf:type |
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lifeskim:mentions |
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pubmed:issue |
11
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pubmed:dateCreated |
1988-3-4
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pubmed:abstractText |
Two affected first cousins with duplication of 15(q22.3----qter) are reported. This resulted from a familial t(8;15)(p23.3;q22.3) translocation. The findings in these patients are compared with each other and with six other published cases. Anthropometric and dermatoglyphic findings are summarised.
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pubmed:commentsCorrections |
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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 |
Nov
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pubmed:issn |
0022-2593
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pubmed:author |
|
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pubmed:issnType |
Print
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pubmed:volume |
24
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
684-7
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pubmed:dateRevised |
2011-11-17
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pubmed:meshHeading |
pubmed-meshheading:3430543-Abnormalities, Multiple,
pubmed-meshheading:3430543-Adult,
pubmed-meshheading:3430543-Child,
pubmed-meshheading:3430543-Chromosome Aberrations,
pubmed-meshheading:3430543-Chromosome Disorders,
pubmed-meshheading:3430543-Chromosome Mapping,
pubmed-meshheading:3430543-Chromosomes, Human, Pair 15,
pubmed-meshheading:3430543-Chromosomes, Human, Pair 8,
pubmed-meshheading:3430543-Female,
pubmed-meshheading:3430543-Humans,
pubmed-meshheading:3430543-Intellectual Disability,
pubmed-meshheading:3430543-Male,
pubmed-meshheading:3430543-Microcephaly,
pubmed-meshheading:3430543-Pedigree,
pubmed-meshheading:3430543-Translocation, Genetic
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pubmed:year |
1987
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pubmed:articleTitle |
Familial t(8;15)(p23.3;q22.3): report of two cases with dup(15) (q22.3----qter).
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pubmed:affiliation |
Department of Medical Genetics, Indiana University School of Medicine, Indianapolis.
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pubmed:publicationType |
Journal Article,
Case Reports
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