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552216
Source:
http://linkedlifedata.com/resource/pubmed/id/552216
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38
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Statements in which the resource exists as a subject.
Predicate
Object
rdf:type
pubmed:Citation
lifeskim:mentions
umls-concept:C0007320
,
umls-concept:C0009566
,
umls-concept:C0039082
,
umls-concept:C0085973
,
umls-concept:C0205494
,
umls-concept:C1260969
pubmed:issue
2
pubmed:dateCreated
1980-12-16
pubmed:abstractText
The first Japanese case of the ring (22) syndrome was described. The patient had diffuse neurological involvement of the central, peripheral nerves and muscles in addition to the phenotypical characteristics of this syndrome.
pubmed:language
eng
pubmed:journal
http://linkedlifedata.com/resource/pubmed/journal/7909235
pubmed:citationSubset
IM
pubmed:status
MEDLINE
pubmed:issn
0387-7604
pubmed:author
pubmed-author:AdachiKK
,
pubmed-author:FukuharaNN
,
pubmed-author:HayashiMM
,
pubmed-author:SakuragawaNN
pubmed:issnType
Print
pubmed:volume
1
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
91-6
pubmed:dateRevised
2004-11-17
pubmed:meshHeading
pubmed-meshheading:552216-Child
,
pubmed-meshheading:552216-Chromosome Deletion
,
pubmed-meshheading:552216-Chromosomes, Human, 21-22 and Y
,
pubmed-meshheading:552216-Humans
,
pubmed-meshheading:552216-Male
,
pubmed-meshheading:552216-Muscle Hypotonia
,
pubmed-meshheading:552216-Muscular Atrophy
,
pubmed-meshheading:552216-Nervous System Diseases
,
pubmed-meshheading:552216-Phenotype
pubmed:year
1979
pubmed:articleTitle
Neurological complications of the ring (22) syndrome: a case report.
pubmed:publicationType
Journal Article
,
Case Reports