4039476

Source:http://linkedlifedata.com/resource/pubmed/id/4039476

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0013336, umls-concept:C0020256, umls-concept:C0020619, umls-concept:C0221423, umls-concept:C0311277, umls-concept:C0439660, umls-concept:C0549491, umls-concept:C1845977
pubmed:issue	1
pubmed:dateCreated	1985-5-28
pubmed:abstractText	Two male patients from one family are reported, who are affected with congenital hydrocephalus, mental retardation, short stature, obesity and hypogenitalism. Most probably the mode of inheritance is X-linked recessive.
pubmed:language	dut
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/7704039
pubmed:citationSubset	IM
pubmed:status	MEDLINE
pubmed:month	Feb
pubmed:issn	0376-7442
pubmed:author	pubmed-author:HamelB CBC, pubmed-author:OttenB JBJ, pubmed-author:SengersR CRC, pubmed-author:de PagterA GAG, pubmed-author:van GilsJ FJF
pubmed:issnType	Print
pubmed:volume	53
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	31-4
pubmed:dateRevised	2011-11-17
pubmed:meshHeading	pubmed-meshheading:4039476-Adolescent, pubmed-meshheading:4039476-Child, pubmed-meshheading:4039476-Dwarfism, pubmed-meshheading:4039476-Female, pubmed-meshheading:4039476-Genes, Recessive, pubmed-meshheading:4039476-Humans, pubmed-meshheading:4039476-Hydrocephalus, pubmed-meshheading:4039476-Hypogonadism, pubmed-meshheading:4039476-Intellectual Disability, pubmed-meshheading:4039476-Male, pubmed-meshheading:4039476-Obesity, pubmed-meshheading:4039476-Pedigree, pubmed-meshheading:4039476-Syndrome, pubmed-meshheading:4039476-X Chromosome
pubmed:year	1985
pubmed:articleTitle	[Congenital hydrocephalus, oligophrenia, dwarfism, centripetal obesity and hypogonadism; an X-linked recessive hereditary illness?].
pubmed:publicationType	Journal Article, English Abstract, Case Reports