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11836373
Source:
http://linkedlifedata.com/resource/pubmed/id/11836373
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43
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Statements in which the resource exists as a subject.
Predicate
Object
rdf:type
pubmed:Citation
lifeskim:mentions
umls-concept:C0162635
,
umls-concept:C0242621
,
umls-concept:C0337493
,
umls-concept:C0678226
,
umls-concept:C1836408
pubmed:issue
2
pubmed:dateCreated
2002-2-11
pubmed:language
eng
pubmed:journal
http://linkedlifedata.com/resource/pubmed/journal/2985087R
pubmed:citationSubset
IM
pubmed:status
MEDLINE
pubmed:month
Feb
pubmed:issn
1468-6244
pubmed:author
pubmed-author:BrunCC
,
pubmed-author:CollM DMD
,
pubmed-author:GabauEE
,
pubmed-author:GuitartMM
,
pubmed-author:MileII
,
pubmed-author:PoyatosDD
,
pubmed-author:VaquerizoJJ
pubmed:issnType
Electronic
pubmed:volume
39
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
E4
pubmed:dateRevised
2008-11-20
pubmed:meshHeading
pubmed-meshheading:11836373-Angelman Syndrome
,
pubmed-meshheading:11836373-Child
,
pubmed-meshheading:11836373-Chromosome Banding
,
pubmed-meshheading:11836373-Chromosomes, Human, Pair 15
,
pubmed-meshheading:11836373-Fatal Outcome
,
pubmed-meshheading:11836373-Humans
,
pubmed-meshheading:11836373-Isochromosomes
,
pubmed-meshheading:11836373-Male
,
pubmed-meshheading:11836373-Phenotype
,
pubmed-meshheading:11836373-Uniparental Disomy
pubmed:year
2002
pubmed:articleTitle
Severe phenotype in Angelman syndrome resulting from paternal isochromosome 15.
pubmed:affiliation
Unidad de Biología Celular, Facultad de Ciencias, Departamento de Biología Celular, Fisiología e Inmunología, Universidad Autónoma de Barcelona, Bellaterra, Barcelona, Spain. David.Poyatos@uab.es
pubmed:publicationType
Journal Article
,
Case Reports
,
Research Support, Non-U.S. Gov't