Switch to
| Predicate | Object |
|---|---|
| rdf:type | |
| lifeskim:mentions | |
| pubmed:issue |
4
|
| pubmed:dateCreated |
1994-11-16
|
| pubmed:abstractText |
Extensive linkage analyses in three families with non-specific X-linked mental retardation (MRX) have localized the gene in each family to the pericentromeric region of the chromosome. The MRX17 gene is localized with a peak lod of 2.41 (theta = 0.0) with the trinucleotide repeat polymorphism at the androgen receptor (AR) gene locus. This gene lies in the interval between the markers DXS255 and DXS990, as defined by recombinants. The MRX18 gene maps to the interval between the markers DXS538 and DXS1126, with a peak lod score of 2.01 (theta = 0.0) at the PFC gene locus. In the third family (Family E) with insufficient informative meioses for assignment of an MRX acronym, the maximum lod score is 1.8 at a recombination fraction of zero for several marker loci between DXS207 and DXS426. Exclusions from the regions of marker loci spanning Xq support the localization of the MRX gene in Family E to the pericentromeric region. Localizations of these and other MRX genes have determined that MRX2 and MRX19 map to distal Xp, MRX3, and MRX6 map to distal Xq, whilst the majority cluster in the pericentromeric region. In addition, we confirm that there are at least two distinct MRX genes near the centromere as delineated by the non-overlapping regional localizations of MRX17 and MRX18. Determination of these non-overlapping localizations is currently the only means of classifying non-syndromal forms of mental retardation and determining the minimum number of MRX loci.
|
| pubmed:language |
eng
|
| pubmed:journal | |
| pubmed:citationSubset |
IM
|
| pubmed:chemical | |
| pubmed:status |
MEDLINE
|
| pubmed:month |
Jul
|
| pubmed:issn |
0148-7299
|
| pubmed:author | |
| pubmed:issnType |
Print
|
| pubmed:day |
15
|
| pubmed:volume |
51
|
| pubmed:geneSymbol |
MRX
|
| pubmed:owner |
NLM
|
| pubmed:authorsComplete |
Y
|
| pubmed:pagination |
553-64
|
| pubmed:dateRevised |
2011-11-17
|
| pubmed:meshHeading |
pubmed-meshheading:7943039-Adolescent,
pubmed-meshheading:7943039-Adult,
pubmed-meshheading:7943039-Centromere,
pubmed-meshheading:7943039-Child,
pubmed-meshheading:7943039-Child, Preschool,
pubmed-meshheading:7943039-Chromosome Mapping,
pubmed-meshheading:7943039-DNA, Satellite,
pubmed-meshheading:7943039-Female,
pubmed-meshheading:7943039-Genetic Heterogeneity,
pubmed-meshheading:7943039-Genetic Linkage,
pubmed-meshheading:7943039-Genetic Markers,
pubmed-meshheading:7943039-Humans,
pubmed-meshheading:7943039-Intellectual Disability,
pubmed-meshheading:7943039-Male,
pubmed-meshheading:7943039-Pedigree,
pubmed-meshheading:7943039-Polymorphism, Genetic,
pubmed-meshheading:7943039-Repetitive Sequences, Nucleic Acid,
pubmed-meshheading:7943039-X Chromosome
|
| pubmed:year |
1994
|
| pubmed:articleTitle |
Pericentromeric genes for non-specific X-linked mental retardation (MRX).
|
| pubmed:affiliation |
Department of Cytogenetics and Molecular Genetics, Women's and Children's Hospital, Australia.
|
| pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
|