Source:http://linkedlifedata.com/resource/pubmed/id/17272211
Switch to
Predicate | Object |
---|---|
rdf:type | |
lifeskim:mentions | |
pubmed:issue |
1
|
pubmed:dateCreated |
2007-2-2
|
pubmed:abstractText |
The fragile X syndrome is the most common form of familial mental retardation. Most males with the FMR1 full mutation function in the mentally retarded range of intelligence. In contrast, females with the FMR1 full mutation show a broader range of intelligence. The most impressive somatic involvement that is consistently found among only premutated carrier females, not full-mutation carriers, is premature ovarian failure (POF).
|
pubmed:language |
eng
|
pubmed:journal | |
pubmed:citationSubset |
IM
|
pubmed:status |
MEDLINE
|
pubmed:month |
Mar
|
pubmed:issn |
1875-6263
|
pubmed:author | |
pubmed:issnType |
Electronic
|
pubmed:volume |
45
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
60-3
|
pubmed:dateRevised |
2011-11-17
|
pubmed:meshHeading |
pubmed-meshheading:17272211-Adult,
pubmed-meshheading:17272211-Child,
pubmed-meshheading:17272211-Female,
pubmed-meshheading:17272211-Fragile X Syndrome,
pubmed-meshheading:17272211-Heterozygote,
pubmed-meshheading:17272211-Humans,
pubmed-meshheading:17272211-Intellectual Disability,
pubmed-meshheading:17272211-Male,
pubmed-meshheading:17272211-Menopause, Premature,
pubmed-meshheading:17272211-Pedigree,
pubmed-meshheading:17272211-Primary Ovarian Insufficiency,
pubmed-meshheading:17272211-Trinucleotide Repeats
|
pubmed:year |
2006
|
pubmed:articleTitle |
Familial premature ovarian failure in female premutated carriers of fragile X syndrome: a case report and literature review.
|
pubmed:affiliation |
Department of Obstetrics and Gynecology, Taipei Veterans General Hospital, and National Yang-Ming University School of Medicine, Taipei, Taiwan.
|
pubmed:publicationType |
Journal Article,
Review,
Case Reports
|