pubmed-article:2732993 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:2732993 | lifeskim:mentions | umls-concept:C1551338 | lld:lifeskim |
pubmed-article:2732993 | lifeskim:mentions | umls-concept:C0265287 | lld:lifeskim |
pubmed-article:2732993 | lifeskim:mentions | umls-concept:C0265349 | lld:lifeskim |
pubmed-article:2732993 | pubmed:issue | 5 | lld:pubmed |
pubmed-article:2732993 | pubmed:dateCreated | 1989-7-27 | lld:pubmed |
pubmed-article:2732993 | pubmed:abstractText | Four unrelated patients are reported with short stature, stiffness of the joints, short fingers, inability to make a fist, and thickened skin on the forearms. Investigations have failed to show a lysosomal storage disorder and radiographs show non-specific changes with a delayed carpal bone age. The clinical features in the four children are very similar to the recently described acromicric dysplasia. There are also similarities to Moore-Federman syndrome which has only been described in one family. The case is made that acromicric dysplasia and Moore-Federman syndrome are the same entity. | lld:pubmed |
pubmed-article:2732993 | pubmed:commentsCorrections | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:2732993 | pubmed:commentsCorrections | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:2732993 | pubmed:commentsCorrections | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:2732993 | pubmed:commentsCorrections | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:2732993 | pubmed:commentsCorrections | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:2732993 | pubmed:language | eng | lld:pubmed |
pubmed-article:2732993 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:2732993 | pubmed:citationSubset | IM | lld:pubmed |
pubmed-article:2732993 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:2732993 | pubmed:month | May | lld:pubmed |
pubmed-article:2732993 | pubmed:issn | 0022-2593 | lld:pubmed |
pubmed-article:2732993 | pubmed:author | pubmed-author:ChallenerJJ | lld:pubmed |
pubmed-article:2732993 | pubmed:author | pubmed-author:BaraitserMM | lld:pubmed |
pubmed-article:2732993 | pubmed:author | pubmed-author:MuellerR FRF | lld:pubmed |
pubmed-article:2732993 | pubmed:author | pubmed-author:PattonM AMA | lld:pubmed |
pubmed-article:2732993 | pubmed:author | pubmed-author:WinterR MRM | lld:pubmed |
pubmed-article:2732993 | pubmed:issnType | Print | lld:pubmed |
pubmed-article:2732993 | pubmed:volume | 26 | lld:pubmed |
pubmed-article:2732993 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:2732993 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:2732993 | pubmed:pagination | 320-5 | lld:pubmed |
pubmed-article:2732993 | pubmed:dateRevised | 2009-11-18 | lld:pubmed |
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pubmed-article:2732993 | pubmed:year | 1989 | lld:pubmed |
pubmed-article:2732993 | pubmed:articleTitle | Moore-Federman syndrome and acromicric dysplasia: are they the same entity? | lld:pubmed |
pubmed-article:2732993 | pubmed:affiliation | Kennedy Galton Centre, Northwick Park Hospital, London. | lld:pubmed |
pubmed-article:2732993 | pubmed:publicationType | Journal Article | lld:pubmed |
http://linkedlifedata.com/r... | pubmed:referesTo | pubmed-article:2732993 | lld:pubmed |
http://linkedlifedata.com/r... | pubmed:referesTo | pubmed-article:2732993 | lld:pubmed |