Switch to
| Predicate | Object |
|---|---|
| rdf:type | |
| lifeskim:mentions | |
| pubmed:issue |
3
|
| pubmed:dateCreated |
1995-10-19
|
| pubmed:abstractText |
The phenotypic nonspecificity of many forms of X-linked mental retardation has hampered attempts to classify them into clinically homogeneous groups. One such condition, described by Clark and Baraitser [1987: Am J Med Genet 26:13-15], has been the subject of a single pedigree report to date. We now describe a further pedigree whose affected members share many manifestations with those reported by Clark and Baraitser, and we consider the possible distinction between this condition and Atkin-Flaitz syndrome.
|
| pubmed:language |
eng
|
| pubmed:journal | |
| pubmed:citationSubset |
IM
|
| pubmed:status |
MEDLINE
|
| pubmed:month |
Jul
|
| pubmed:issn |
0148-7299
|
| pubmed:author | |
| pubmed:issnType |
Print
|
| pubmed:day |
3
|
| pubmed:volume |
57
|
| pubmed:owner |
NLM
|
| pubmed:authorsComplete |
Y
|
| pubmed:pagination |
380-4
|
| pubmed:dateRevised |
2011-11-17
|
| pubmed:meshHeading |
pubmed-meshheading:7677138-Brain,
pubmed-meshheading:7677138-Child,
pubmed-meshheading:7677138-Child, Preschool,
pubmed-meshheading:7677138-Female,
pubmed-meshheading:7677138-Genetic Linkage,
pubmed-meshheading:7677138-Heterozygote Detection,
pubmed-meshheading:7677138-Humans,
pubmed-meshheading:7677138-Intellectual Disability,
pubmed-meshheading:7677138-Male,
pubmed-meshheading:7677138-Obesity,
pubmed-meshheading:7677138-Pedigree,
pubmed-meshheading:7677138-X Chromosome
|
| pubmed:year |
1995
|
| pubmed:articleTitle |
Nonspecific X-linked mental retardation with macrocephaly and obesity: a further family.
|
| pubmed:affiliation |
Department of Paediatric Genetics, Hospital for Sick Children, London, United Kingdom.
|
| pubmed:publicationType |
Journal Article,
Case Reports
|