| pubmed-article:890117 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:890117 | lifeskim:mentions | umls-concept:C0019425 | lld:lifeskim |
| pubmed-article:890117 | lifeskim:mentions | umls-concept:C0406702 | lld:lifeskim |
| pubmed-article:890117 | pubmed:issue | 3C | lld:pubmed |
| pubmed-article:890117 | pubmed:dateCreated | 1977-10-14 | lld:pubmed |
| pubmed-article:890117 | pubmed:abstractText | Sweat pores on the epidermal ridges are hypoplastic and reduced in number in three sisters affected with autosomal recessive hypohidrotic dysplasia. The heterozygote state is expressed by a reduced number of qualitatively normal sweat pores (14.07 +/- 8.59 as compared to 22.27 +/- 2.33 in controls). Clinical and genetic considerations suggest that this may be a distinct type that has to be differentiated from other autosomal recessive hypohidrotic ectodermal dysplasias. Heterozygote manifestation may contribute to delineate this groups of disorders further. | lld:pubmed |
| pubmed-article:890117 | pubmed:language | eng | lld:pubmed |
| pubmed-article:890117 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:890117 | pubmed:citationSubset | IM | lld:pubmed |
| pubmed-article:890117 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:890117 | pubmed:issn | 0547-6844 | lld:pubmed |
| pubmed-article:890117 | pubmed:author | pubmed-author:PassargeEE | lld:pubmed |
| pubmed-article:890117 | pubmed:author | pubmed-author:FrielJJ | lld:pubmed |
| pubmed-article:890117 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:890117 | pubmed:volume | 13 | lld:pubmed |
| pubmed-article:890117 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:890117 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:890117 | pubmed:pagination | 95-100 | lld:pubmed |
| pubmed-article:890117 | pubmed:dateRevised | 2004-11-17 | lld:pubmed |
| pubmed-article:890117 | pubmed:meshHeading | pubmed-meshheading:890117-H... | lld:pubmed |
| pubmed-article:890117 | pubmed:meshHeading | pubmed-meshheading:890117-A... | lld:pubmed |
| pubmed-article:890117 | pubmed:meshHeading | pubmed-meshheading:890117-F... | lld:pubmed |
| pubmed-article:890117 | pubmed:meshHeading | pubmed-meshheading:890117-F... | lld:pubmed |
| pubmed-article:890117 | pubmed:meshHeading | pubmed-meshheading:890117-G... | lld:pubmed |
| pubmed-article:890117 | pubmed:meshHeading | pubmed-meshheading:890117-A... | lld:pubmed |
| pubmed-article:890117 | pubmed:meshHeading | pubmed-meshheading:890117-A... | lld:pubmed |
| pubmed-article:890117 | pubmed:meshHeading | pubmed-meshheading:890117-E... | lld:pubmed |
| pubmed-article:890117 | pubmed:meshHeading | pubmed-meshheading:890117-C... | lld:pubmed |
| pubmed-article:890117 | pubmed:meshHeading | pubmed-meshheading:890117-P... | lld:pubmed |
| pubmed-article:890117 | pubmed:meshHeading | pubmed-meshheading:890117-H... | lld:pubmed |
| pubmed-article:890117 | pubmed:meshHeading | pubmed-meshheading:890117-H... | lld:pubmed |
| pubmed-article:890117 | pubmed:year | 1977 | lld:pubmed |
| pubmed-article:890117 | pubmed:articleTitle | Autosomal recessive hypohidrotic ectodermal dysplasia with subclinical manifestation in the heterozygote. | lld:pubmed |
| pubmed-article:890117 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:890117 | pubmed:publicationType | Case Reports | lld:pubmed |
| http://linkedlifedata.com/r... | pubmed:referesTo | pubmed-article:890117 | lld:pubmed |
| http://linkedlifedata.com/r... | pubmed:referesTo | pubmed-article:890117 | lld:pubmed |
| http://linkedlifedata.com/r... | pubmed:referesTo | pubmed-article:890117 | lld:pubmed |
