4733656

Source:http://linkedlifedata.com/resource/pubmed/id/4733656

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0020676
pubmed:issue	5
pubmed:dateCreated	1973-11-30
pubmed:language	fre
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/0372421
pubmed:citationSubset	IM
pubmed:status	MEDLINE
pubmed:month	May
pubmed:issn	0003-9764
pubmed:author	pubmed-author:BattinJJ, pubmed-author:MarchandJ CJC, pubmed-author:ServilleFF
pubmed:issnType	Print
pubmed:volume	30
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	548
pubmed:dateRevised	2004-11-17
pubmed:meshHeading	pubmed-meshheading:4733656-Child, Preschool, pubmed-meshheading:4733656-Chromosome Aberrations, pubmed-meshheading:4733656-Chromosome Disorders, pubmed-meshheading:4733656-Chromosomes, Human, 16-18, pubmed-meshheading:4733656-Dermatoglyphics, pubmed-meshheading:4733656-Female, pubmed-meshheading:4733656-Humans, pubmed-meshheading:4733656-Hypothyroidism, pubmed-meshheading:4733656-Karyotyping
pubmed:year	1973
pubmed:articleTitle	[18 p-syndrome and hypothyroidism].
pubmed:publicationType	Journal Article, Case Reports