|
rdf:type |
|
|
lifeskim:mentions |
umls-concept:C0015576,
umls-concept:C0033920,
umls-concept:C0205210,
umls-concept:C0750540,
umls-concept:C0796215,
umls-concept:C0796244,
umls-concept:C0796345,
umls-concept:C1136249,
umls-concept:C1274040,
umls-concept:C1417296,
umls-concept:C1511726,
umls-concept:C1845298,
umls-concept:C1845333,
umls-concept:C2699121
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|
pubmed:issue |
3
|
|
pubmed:dateCreated |
2000-5-17
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|
pubmed:abstractText |
Four families are described in which mental retardation segregates in an X-linked fashion. Mental retardation was the only consistent clinical finding in all affected males. The degree of retardation varied from mild to profound both between and within families. Linkage analysis localized the genetic defect of MRX43 to Xp22. 31-p21.2, MRX44 to Xp11.3-p11.21, MRX45 to Xp11.3-p11.21, and MRX52 to Xp11.21-q21.33 with LOD scores of >2 at straight theta = 0.0 in all four families.
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|
pubmed:language |
eng
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|
pubmed:journal |
|
|
pubmed:citationSubset |
IM
|
|
pubmed:chemical |
|
|
pubmed:status |
MEDLINE
|
|
pubmed:month |
Jul
|
|
pubmed:issn |
0148-7299
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|
pubmed:author |
pubmed-author:Assman-HulsmansC FCF,
pubmed-author:HamelB CBC,
pubmed-author:KnoersN VNV,
pubmed-author:KremerHH,
pubmed-author:MarimanE CEC,
pubmed-author:RopersH HHH,
pubmed-author:SmeetsD FDF,
pubmed-author:SmitsA PAP,
pubmed-author:ThoonenG HGH,
pubmed-author:van RoosmalenTT,
pubmed-author:van den HelmBB
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pubmed:copyrightInfo |
Copyright 1999 Wiley-Liss, Inc.
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|
pubmed:issnType |
Print
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|
pubmed:day |
30
|
|
pubmed:volume |
85
|
|
pubmed:owner |
NLM
|
|
pubmed:authorsComplete |
Y
|
|
pubmed:pagination |
290-304
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|
pubmed:dateRevised |
2011-11-17
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pubmed:meshHeading |
pubmed-meshheading:10398246-Adult,
pubmed-meshheading:10398246-Aged,
pubmed-meshheading:10398246-Chromosome Mapping,
pubmed-meshheading:10398246-DNA,
pubmed-meshheading:10398246-Family Health,
pubmed-meshheading:10398246-Fatal Outcome,
pubmed-meshheading:10398246-Female,
pubmed-meshheading:10398246-Follow-Up Studies,
pubmed-meshheading:10398246-Genetic Linkage,
pubmed-meshheading:10398246-Humans,
pubmed-meshheading:10398246-Intellectual Disability,
pubmed-meshheading:10398246-Lod Score,
pubmed-meshheading:10398246-Male,
pubmed-meshheading:10398246-Microsatellite Repeats,
pubmed-meshheading:10398246-Middle Aged,
pubmed-meshheading:10398246-Pedigree,
pubmed-meshheading:10398246-Psychiatric Status Rating Scales,
pubmed-meshheading:10398246-Psychometrics,
pubmed-meshheading:10398246-X Chromosome
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|
pubmed:year |
1999
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|
pubmed:articleTitle |
Four families (MRX43, MRX44, MRX45, MRX52) with nonspecific X-linked mental retardation: clinical and psychometric data and results of linkage analysis.
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|
pubmed:affiliation |
Department of Human Genetics, University Hospital, Nijmegen, The Netherlands. b.hamel@antrg.azn.nl
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pubmed:publicationType |
Journal Article,
Case Reports,
Research Support, Non-U.S. Gov't
|
