4998085

Source:http://linkedlifedata.com/resource/pubmed/id/4998085

Download in:

Switch to

Custom View

Named Graph Language Inference

Statements in which the resource exists as a subject.
Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0000768, umls-concept:C0012634, umls-concept:C0026010, umls-concept:C0039082, umls-concept:C0241764
pubmed:issue	5
pubmed:dateCreated	1971-10-7
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/0370500
pubmed:citationSubset	AIM
pubmed:status	MEDLINE
pubmed:month	May
pubmed:issn	0002-9394
pubmed:author	pubmed-author:GoldbergM FMF, pubmed-author:McKusickV AVA
pubmed:issnType	Print
pubmed:volume	71
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	1128-33
pubmed:dateRevised	2011-11-17
pubmed:meshHeading	pubmed-meshheading:4998085-Abnormalities, Multiple, pubmed-meshheading:4998085-Adolescent, pubmed-meshheading:4998085-Adult, pubmed-meshheading:4998085-Blepharoptosis, pubmed-meshheading:4998085-Child, pubmed-meshheading:4998085-Child, Preschool, pubmed-meshheading:4998085-Coloboma, pubmed-meshheading:4998085-Diastema, pubmed-meshheading:4998085-Ear, External, pubmed-meshheading:4998085-Eye Abnormalities, pubmed-meshheading:4998085-Female, pubmed-meshheading:4998085-Foot Deformities, Congenital, pubmed-meshheading:4998085-Genetic Linkage, pubmed-meshheading:4998085-Growth Disorders, pubmed-meshheading:4998085-Humans, pubmed-meshheading:4998085-Infant, pubmed-meshheading:4998085-Infant, Newborn, pubmed-meshheading:4998085-Intellectual Disability, pubmed-meshheading:4998085-Maine, pubmed-meshheading:4998085-Male, pubmed-meshheading:4998085-Microcephaly, pubmed-meshheading:4998085-Microphthalmos, pubmed-meshheading:4998085-Middle Aged, pubmed-meshheading:4998085-Nystagmus, Pathologic, pubmed-meshheading:4998085-Pedigree, pubmed-meshheading:4998085-Sex Chromosomes, pubmed-meshheading:4998085-Strabismus
pubmed:year	1971
pubmed:articleTitle	X-linked colobomatous microphthalmos and other congenital anomalies. A disorder resembling Lenz's dysmorphogenetic syndrome.
pubmed:publicationType	Journal Article