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rdf:type |
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lifeskim:mentions |
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pubmed:issue |
12
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pubmed:dateCreated |
2002-9-19
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pubmed:abstractText |
Many observations indicate that genetic factors play an important role in the aetiology of autism. Up to now, however, no genetic markers have been convincingly identified which influence the predisposition to this disorder. Complex genetic analysis of autistic patients and their families may therefore lead to the identification of features which could help to direct further search for the predisposing genes.
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pubmed:language |
cze
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pubmed:journal |
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pubmed:citationSubset |
IM
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pubmed:chemical |
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pubmed:status |
MEDLINE
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pubmed:month |
Jun
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pubmed:issn |
0008-7335
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pubmed:author |
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pubmed:issnType |
Print
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pubmed:day |
21
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pubmed:volume |
141
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
381-7
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:12238024-Adolescent,
pubmed-meshheading:12238024-Adult,
pubmed-meshheading:12238024-Autistic Disorder,
pubmed-meshheading:12238024-Child,
pubmed-meshheading:12238024-Child, Preschool,
pubmed-meshheading:12238024-Cytogenetic Analysis,
pubmed-meshheading:12238024-Female,
pubmed-meshheading:12238024-Fragile X Mental Retardation Protein,
pubmed-meshheading:12238024-Genetic Predisposition to Disease,
pubmed-meshheading:12238024-Humans,
pubmed-meshheading:12238024-Male,
pubmed-meshheading:12238024-Nerve Tissue Proteins,
pubmed-meshheading:12238024-Pedigree,
pubmed-meshheading:12238024-RNA-Binding Proteins,
pubmed-meshheading:12238024-Trinucleotide Repeats
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pubmed:year |
2002
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pubmed:articleTitle |
[Genetic study of 20 patients with autism disorders].
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pubmed:affiliation |
Ustav biologie a lékarské genetiky, LF UK a FNM, Praha. marketa.havlovicova@lfmotol.cuni.cz
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pubmed:publicationType |
Journal Article,
English Abstract,
Research Support, Non-U.S. Gov't
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