7486832

Source:http://linkedlifedata.com/resource/pubmed/id/7486832

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C1850318
pubmed:issue	2
pubmed:dateCreated	1995-11-29
pubmed:abstractText	The authors report on a new case of omodysplasia with severe shortness of lower limbs and with first cousin parents. This condition is a second form of omodysplasia. Recessive transmission is confirmed by consanguinity.
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/0370562
pubmed:citationSubset	IM
pubmed:status	MEDLINE
pubmed:issn	0003-3995
pubmed:author	pubmed-author:PennerathAA, pubmed-author:PoiratPP, pubmed-author:StollCC
pubmed:issnType	Print
pubmed:volume	38
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	97-101
pubmed:dateRevised	2005-11-16
pubmed:meshHeading	pubmed-meshheading:7486832-Abnormalities, Multiple, pubmed-meshheading:7486832-Adult, pubmed-meshheading:7486832-Consanguinity, pubmed-meshheading:7486832-Dwarfism, pubmed-meshheading:7486832-Facies, pubmed-meshheading:7486832-Female, pubmed-meshheading:7486832-Femur, pubmed-meshheading:7486832-Genes, Recessive, pubmed-meshheading:7486832-Genetic Heterogeneity, pubmed-meshheading:7486832-Humans, pubmed-meshheading:7486832-Humerus, pubmed-meshheading:7486832-Infant, Newborn, pubmed-meshheading:7486832-Osteochondrodysplasias, pubmed-meshheading:7486832-Pedigree
pubmed:year	1995
pubmed:articleTitle	Autosomal recessive omodysplasia.
pubmed:affiliation	Centre Hospitalo-Universitaire, Institut de Puériculture, Strasbourg, France.
pubmed:publicationType	Journal Article, Review, Case Reports