3688033

Source:http://linkedlifedata.com/resource/pubmed/id/3688033

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0001080, umls-concept:C0017382, umls-concept:C0034897, umls-concept:C0241888
pubmed:issue	4
pubmed:dateCreated	1988-1-21
pubmed:abstractText	Two additional pedigrees with familial recurrence of achondroplasia are described. Genetic risk for children of sibs of affected individuals or premutation carriers seems to be low, but it is advisable to monitor at risk pregnancies by midtrimester ultrasonography to diagnose fetal achondroplasia.
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/7708900
pubmed:citationSubset	IM
pubmed:status	MEDLINE
pubmed:month	Dec
pubmed:issn	0148-7299
pubmed:author	pubmed-author:DodinvalPP, pubmed-author:Le MarecBB
pubmed:issnType	Print
pubmed:volume	28
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	949-54
pubmed:dateRevised	2004-11-17
pubmed:meshHeading	pubmed-meshheading:3688033-Achondroplasia, pubmed-meshheading:3688033-Adult, pubmed-meshheading:3688033-Aged, pubmed-meshheading:3688033-Female, pubmed-meshheading:3688033-Genetic Counseling, pubmed-meshheading:3688033-Heterozygote Detection, pubmed-meshheading:3688033-Humans, pubmed-meshheading:3688033-Mutation, pubmed-meshheading:3688033-Pedigree, pubmed-meshheading:3688033-Recurrence, pubmed-meshheading:3688033-Risk Factors
pubmed:year	1987
pubmed:articleTitle	Genetic counselling in unexpected familial recurrence of achondroplasia.
pubmed:affiliation	Department of Human Genetics, University of Liege, Belgium.
pubmed:publicationType	Journal Article, Case Reports