Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
3
pubmed:dateCreated
1995-7-20
pubmed:abstractText
Mental impairment and instability of the CCG repeat at FRAXE is described in six kindreds. Cosegregation of FRAXA and FRAXE was found within one of these kindreds. Cytogenetic expression of FRAXE was shown to skip a generation when associated with a reduction in size of the CCG expansion when transmitted through a male; however, in general, transmission occurred through females and a copy number increased from one generation to the next. In these respects the behaviour of FRAXE paralleled that of FRAXA. A relationship between FRAXE and non-specific mental impairment is strongly suggested by the occurrence in these families of more mentally impaired male and female carriers, after removal of index cases, than could reasonably be expected by chance.
pubmed:commentsCorrections
http://linkedlifedata.com/resource/pubmed/commentcorrection/7783162-1284466, http://linkedlifedata.com/resource/pubmed/commentcorrection/7783162-1302021, http://linkedlifedata.com/resource/pubmed/commentcorrection/7783162-1307252, http://linkedlifedata.com/resource/pubmed/commentcorrection/7783162-1619631, http://linkedlifedata.com/resource/pubmed/commentcorrection/7783162-1633644, http://linkedlifedata.com/resource/pubmed/commentcorrection/7783162-1710175, http://linkedlifedata.com/resource/pubmed/commentcorrection/7783162-1878973, http://linkedlifedata.com/resource/pubmed/commentcorrection/7783162-2138257, http://linkedlifedata.com/resource/pubmed/commentcorrection/7783162-3605224, http://linkedlifedata.com/resource/pubmed/commentcorrection/7783162-3674104, http://linkedlifedata.com/resource/pubmed/commentcorrection/7783162-6118659, http://linkedlifedata.com/resource/pubmed/commentcorrection/7783162-7874164, http://linkedlifedata.com/resource/pubmed/commentcorrection/7783162-7977354, http://linkedlifedata.com/resource/pubmed/commentcorrection/7783162-7981744, http://linkedlifedata.com/resource/pubmed/commentcorrection/7783162-8023854, http://linkedlifedata.com/resource/pubmed/commentcorrection/7783162-8034308, http://linkedlifedata.com/resource/pubmed/commentcorrection/7783162-8093512, http://linkedlifedata.com/resource/pubmed/commentcorrection/7783162-8213832, http://linkedlifedata.com/resource/pubmed/commentcorrection/7783162-8242063, http://linkedlifedata.com/resource/pubmed/commentcorrection/7783162-8255475, http://linkedlifedata.com/resource/pubmed/commentcorrection/7783162-8334699, http://linkedlifedata.com/resource/pubmed/commentcorrection/7783162-8348152, http://linkedlifedata.com/resource/pubmed/commentcorrection/7783162-8445629, http://linkedlifedata.com/resource/pubmed/commentcorrection/7783162-8462194, http://linkedlifedata.com/resource/pubmed/commentcorrection/7783162-8499907
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:status
MEDLINE
pubmed:month
Mar
pubmed:issn
0022-2593
pubmed:author
pubmed:issnType
Print
pubmed:volume
32
pubmed:geneSymbol
FMR1
pubmed:owner
NLM
pubmed:authorsComplete
N
pubmed:pagination
162-9
pubmed:dateRevised
2011-11-17
pubmed:meshHeading
pubmed-meshheading:7783162-Adolescent, pubmed-meshheading:7783162-Adult, pubmed-meshheading:7783162-Aged, pubmed-meshheading:7783162-Blotting, Southern, pubmed-meshheading:7783162-Child, pubmed-meshheading:7783162-Chromosome Fragility, pubmed-meshheading:7783162-Cytogenetics, pubmed-meshheading:7783162-Family Health, pubmed-meshheading:7783162-Female, pubmed-meshheading:7783162-Fragile X Syndrome, pubmed-meshheading:7783162-Heterozygote, pubmed-meshheading:7783162-Humans, pubmed-meshheading:7783162-In Situ Hybridization, Fluorescence, pubmed-meshheading:7783162-Intellectual Disability, pubmed-meshheading:7783162-Intelligence, pubmed-meshheading:7783162-Intelligence Tests, pubmed-meshheading:7783162-Male, pubmed-meshheading:7783162-Middle Aged, pubmed-meshheading:7783162-Pedigree, pubmed-meshheading:7783162-Phenotype, pubmed-meshheading:7783162-Polymerase Chain Reaction, pubmed-meshheading:7783162-Repetitive Sequences, Nucleic Acid, pubmed-meshheading:7783162-X Chromosome
pubmed:year
1995
pubmed:articleTitle
FRAXE and mental retardation.
pubmed:affiliation
Centre for Medical Genetics, Cytogenetics and Molecular Genetics, Women's and Children's Hospital, Adelaide, Australia.
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't