8558551

Source:http://linkedlifedata.com/resource/pubmed/id/8558551

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0016667, umls-concept:C0031437, umls-concept:C0205246, umls-concept:C0596611, umls-concept:C1414649, umls-concept:C1849265, umls-concept:C2827666
pubmed:issue	10
pubmed:dateCreated	1996-2-28
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pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/2985087R
pubmed:citationSubset	IM
pubmed:chemical	http://linkedlifedata.com/resource/pubmed/chemical/FMR1 protein, human, http://linkedlifedata.com/resource/pubmed/chemical/Fragile X Mental Retardation Protein, http://linkedlifedata.com/resource/pubmed/chemical/Insulin-Like Growth Factor Binding..., http://linkedlifedata.com/resource/pubmed/chemical/Insulin-Like Growth Factor I, http://linkedlifedata.com/resource/pubmed/chemical/Nerve Tissue Proteins, http://linkedlifedata.com/resource/pubmed/chemical/RNA-Binding Proteins
pubmed:status	MEDLINE
pubmed:month	Oct
pubmed:issn	0022-2593
pubmed:author	pubmed-author:DijkstraP FPF, pubmed-author:HalleyD JDJ, pubmed-author:NiermeijerM FMF, pubmed-author:OostraB ABA, pubmed-author:RobinsonHH, pubmed-author:Stolte-DijkstraII, pubmed-author:Tjon Pian GiC VCV, pubmed-author:TurnerGG, pubmed-author:de VriesB BBB, pubmed-author:van DoornJJ
pubmed:issnType	Print
pubmed:volume	32
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	764-9
pubmed:dateRevised	2009-11-18
pubmed:meshHeading	pubmed-meshheading:8558551-Adult, pubmed-meshheading:8558551-Child, Preschool, pubmed-meshheading:8558551-Fragile X Mental Retardation Protein, pubmed-meshheading:8558551-Fragile X Syndrome, pubmed-meshheading:8558551-Growth Disorders, pubmed-meshheading:8558551-Humans, pubmed-meshheading:8558551-Insulin-Like Growth Factor Binding Protein 3, pubmed-meshheading:8558551-Insulin-Like Growth Factor I, pubmed-meshheading:8558551-Male, pubmed-meshheading:8558551-Mutation, pubmed-meshheading:8558551-Nerve Tissue Proteins, pubmed-meshheading:8558551-Pedigree, pubmed-meshheading:8558551-Phenotype, pubmed-meshheading:8558551-RNA-Binding Proteins
pubmed:year	1995
pubmed:articleTitle	General overgrowth in the fragile X syndrome: variability in the phenotypic expression of the FMR1 gene mutation.
pubmed:affiliation	Department of Clinical Genetics, University Hospital Dijkzigt, Rotterdam, The Netherlands.
pubmed:publicationType	Journal Article, Case Reports