rdf:type |
|
lifeskim:mentions |
|
pubmed:issue |
1-2
|
pubmed:dateCreated |
1988-11-8
|
pubmed:abstractText |
We describe a family with a syndrome of mental retardation, dystonic movements of the hands and dysarthria inherited in an X-linked recessive pattern. DNA marker studies gave a maximum lod score of 2.11 at theta of 0.00 for DXS41 with a likely localization of the gene to Xpter----Xp21.
|
pubmed:language |
eng
|
pubmed:journal |
|
pubmed:citationSubset |
IM
|
pubmed:chemical |
|
pubmed:status |
MEDLINE
|
pubmed:issn |
0148-7299
|
pubmed:author |
|
pubmed:issnType |
Print
|
pubmed:volume |
30
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
251-62
|
pubmed:dateRevised |
2011-11-17
|
pubmed:meshHeading |
pubmed-meshheading:3177452-Adolescent,
pubmed-meshheading:3177452-Adult,
pubmed-meshheading:3177452-Child,
pubmed-meshheading:3177452-Child, Preschool,
pubmed-meshheading:3177452-DNA Probes,
pubmed-meshheading:3177452-Dystonia,
pubmed-meshheading:3177452-Female,
pubmed-meshheading:3177452-Genetic Linkage,
pubmed-meshheading:3177452-Genetic Markers,
pubmed-meshheading:3177452-Hand,
pubmed-meshheading:3177452-Humans,
pubmed-meshheading:3177452-Intellectual Disability,
pubmed-meshheading:3177452-Male,
pubmed-meshheading:3177452-Middle Aged,
pubmed-meshheading:3177452-Pedigree,
pubmed-meshheading:3177452-Syndrome,
pubmed-meshheading:3177452-X Chromosome
|
pubmed:articleTitle |
X-linked mental retardation with dystonic movements of the hands.
|
pubmed:affiliation |
Department of Medical Genetics, Prince of Wales Children's Hospital, Randwick, Sydney, New South Wales.
|
pubmed:publicationType |
Journal Article,
Case Reports,
Research Support, Non-U.S. Gov't
|