| pubmed-article:17626606 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:17626606 | lifeskim:mentions | umls-concept:C0020796 | lld:lifeskim |
| pubmed-article:17626606 | lifeskim:mentions | umls-concept:C0260267 | lld:lifeskim |
| pubmed-article:17626606 | lifeskim:mentions | umls-concept:C0162635 | lld:lifeskim |
| pubmed-article:17626606 | lifeskim:mentions | umls-concept:C0032897 | lld:lifeskim |
| pubmed-article:17626606 | lifeskim:mentions | umls-concept:C0220908 | lld:lifeskim |
| pubmed-article:17626606 | lifeskim:mentions | umls-concept:C0205081 | lld:lifeskim |
| pubmed-article:17626606 | lifeskim:mentions | umls-concept:C0039260 | lld:lifeskim |
| pubmed-article:17626606 | lifeskim:mentions | umls-concept:C1710133 | lld:lifeskim |
| pubmed-article:17626606 | pubmed:issue | 2 | lld:pubmed |
| pubmed-article:17626606 | pubmed:dateCreated | 2007-7-13 | lld:pubmed |
| pubmed-article:17626606 | pubmed:abstractText | Prader-Willi syndrome (PWS) and Angelman syndrome (AS) are caused by deficiencies of gene expression from paternal or maternal chromosome 15q11-q13, respectively. The study was conducted to estimate the prevalence of PWS and AS in children with moderate to profound mental retardation in Taiwan. | lld:pubmed |
| pubmed-article:17626606 | pubmed:language | eng | lld:pubmed |
| pubmed-article:17626606 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:17626606 | pubmed:citationSubset | IM | lld:pubmed |
| pubmed-article:17626606 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:17626606 | pubmed:issn | 1608-8115 | lld:pubmed |
| pubmed-article:17626606 | pubmed:author | pubmed-author:KuoPao-LinPL | lld:pubmed |
| pubmed-article:17626606 | pubmed:author | pubmed-author:SuMei-TszMT | lld:pubmed |
| pubmed-article:17626606 | pubmed:author | pubmed-author:TengYeng-NiYN | lld:pubmed |
| pubmed-article:17626606 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:17626606 | pubmed:volume | 48 | lld:pubmed |
| pubmed-article:17626606 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:17626606 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:17626606 | pubmed:pagination | 73-6 | lld:pubmed |
| pubmed-article:17626606 | pubmed:dateRevised | 2011-11-17 | lld:pubmed |
| pubmed-article:17626606 | pubmed:meshHeading | pubmed-meshheading:17626606... | lld:pubmed |
| pubmed-article:17626606 | pubmed:meshHeading | pubmed-meshheading:17626606... | lld:pubmed |
| pubmed-article:17626606 | pubmed:meshHeading | pubmed-meshheading:17626606... | lld:pubmed |
| pubmed-article:17626606 | pubmed:meshHeading | pubmed-meshheading:17626606... | lld:pubmed |
| pubmed-article:17626606 | pubmed:meshHeading | pubmed-meshheading:17626606... | lld:pubmed |
| pubmed-article:17626606 | pubmed:meshHeading | pubmed-meshheading:17626606... | lld:pubmed |
| pubmed-article:17626606 | pubmed:meshHeading | pubmed-meshheading:17626606... | lld:pubmed |
| pubmed-article:17626606 | pubmed:meshHeading | pubmed-meshheading:17626606... | lld:pubmed |
| pubmed-article:17626606 | pubmed:meshHeading | pubmed-meshheading:17626606... | lld:pubmed |
| pubmed-article:17626606 | pubmed:meshHeading | pubmed-meshheading:17626606... | lld:pubmed |
| pubmed-article:17626606 | pubmed:meshHeading | pubmed-meshheading:17626606... | lld:pubmed |
| pubmed-article:17626606 | pubmed:articleTitle | Screening of Prader-Willi syndrome and Angelman syndrome in school children with moderate to profound mental retardation in southern Taiwan. | lld:pubmed |
| pubmed-article:17626606 | pubmed:affiliation | Department of Obstetrics and Gynecology, National Cheng-Kung University Medical College, Tainan, Taiwan. | lld:pubmed |
| pubmed-article:17626606 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:17626606 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
