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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 |
1989-12-26
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pubmed:abstractText |
We describe the clinical and cytogenetic findings in a boy with an unbalanced karyotype involving monosomy for 3q27-q29. He does not resemble other reported cases of del(3q). Deletions of the long arm of chromosome 3 are extremely rare, having been reported in five cases, only two of which had terminal 3q deletions.
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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 |
|
|
pubmed:issnType |
Print
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pubmed:volume |
26
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
729-30
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pubmed:dateRevised |
2009-11-18
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pubmed:meshHeading |
pubmed-meshheading:2479748-Child,
pubmed-meshheading:2479748-Chromosome Deletion,
pubmed-meshheading:2479748-Chromosomes, Human, Pair 3,
pubmed-meshheading:2479748-Developmental Disabilities,
pubmed-meshheading:2479748-Facial Bones,
pubmed-meshheading:2479748-Growth Disorders,
pubmed-meshheading:2479748-Humans,
pubmed-meshheading:2479748-Karyotyping,
pubmed-meshheading:2479748-Male,
pubmed-meshheading:2479748-Skull
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pubmed:year |
1989
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|
pubmed:articleTitle |
Partial monosomy 3q in a boy with short stature, developmental delay, and mild dysmorphic features.
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|
pubmed:affiliation |
Kennedy Galton Centre, Northwick Park Hospital, Harrow, Middlesex.
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pubmed:publicationType |
Journal Article,
Review,
Case Reports
|
