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rdf:type |
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lifeskim:mentions |
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pubmed:issue |
4
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pubmed:dateCreated |
1991-8-28
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pubmed:abstractText |
Two sibs with a phenotype characterised by short stature, brachydactyly, and ocular anomalies (Peters' anomaly) are reported (Peters'-plus syndrome). The consanguinity is in agreement with the proposed autosomal recessive inheritance.
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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 |
Apr
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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 |
28
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
277-9
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pubmed:dateRevised |
2009-11-18
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pubmed:meshHeading |
pubmed-meshheading:1856836-Child, Preschool,
pubmed-meshheading:1856836-Consanguinity,
pubmed-meshheading:1856836-Cornea,
pubmed-meshheading:1856836-Female,
pubmed-meshheading:1856836-Genes, Recessive,
pubmed-meshheading:1856836-Growth Disorders,
pubmed-meshheading:1856836-Humans,
pubmed-meshheading:1856836-Infant,
pubmed-meshheading:1856836-Male,
pubmed-meshheading:1856836-Phenotype,
pubmed-meshheading:1856836-Syndrome
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pubmed:year |
1991
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pubmed:articleTitle |
Short stature, brachydactyly, and Peters' anomaly (Peters'-plus syndrome): confirmation of autosomal recessive inheritance.
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pubmed:affiliation |
Centro de Genética Médica, Instituto Fernandes Figueira, Rio de Janeiro, Brazil.
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pubmed:publicationType |
Journal Article,
Case Reports,
Research Support, Non-U.S. Gov't
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