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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
11
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pubmed:dateCreated |
1984-12-11
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pubmed:abstractText |
Clinical records, autopsy reports, and microscopic slides from 11 infants with the recombinant 8 syndrome, an inherited abnormality of chromosome 8 affecting Hispanics from New Mexico and Colorado, were evaluated. A prevalence of cardiac and genitourinary anomalies was found, while few central nervous system abnormalities were observed. Dysmorphic features associated with recombinant 8 syndrome are presented, with descriptions of the inheritance pattern and recurrence risk. Because recombinant 8 syndrome is a chromosomal disorder that will appear more and more frequently as kindreds enlarge, pathologists must be alert to its diagnostic characteristics and genetic implications.
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pubmed:grant | |
pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:status |
MEDLINE
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pubmed:month |
Nov
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pubmed:issn |
0046-8177
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
15
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
1080-4
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pubmed:dateRevised |
2007-11-14
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pubmed:meshHeading |
pubmed-meshheading:6490002-Abnormalities, Multiple,
pubmed-meshheading:6490002-Chromosome Aberrations,
pubmed-meshheading:6490002-Chromosome Banding,
pubmed-meshheading:6490002-Chromosome Disorders,
pubmed-meshheading:6490002-Chromosomes, Human, 6-12 and X,
pubmed-meshheading:6490002-Female,
pubmed-meshheading:6490002-Humans,
pubmed-meshheading:6490002-Infant,
pubmed-meshheading:6490002-Infant, Newborn,
pubmed-meshheading:6490002-Karyotyping,
pubmed-meshheading:6490002-Male,
pubmed-meshheading:6490002-Recombination, Genetic,
pubmed-meshheading:6490002-Syndrome
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pubmed:year |
1984
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pubmed:articleTitle |
Clinicopathologic and dysmorphic findings in recombinant chromosome 8 syndrome.
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pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, P.H.S.,
Research Support, Non-U.S. Gov't
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