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- Q7243682 subject Q6853484.
- Q7243682 subject Q7031586.
- Q7243682 subject Q9915528.
- Q7243682 abstract "Primrose syndrome is a rare, slowly progressive genetic disorder that can vary symptomatically between individual cases, but is generally characterised by ossification of the external ears, learning difficulties, and facial abnormalities. It was first described in 1982 in Scotland's Royal National Larbert Institution by Dr D.A.A. Primrose.Primrose syndrome appears to occur spontaneously, regardless of family history. The cause is currently unknown and there are no known treatments.".
- Q7243682 omim "259050".
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- Q7243682 wikiPageWikiLink Q6853484.
- Q7243682 wikiPageWikiLink Q7031586.
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- Q7243682 wikiPageWikiLink Q9915528.
- Q7243682 name "Primrose syndrome".
- Q7243682 omim "259050".
- Q7243682 type Disease.
- Q7243682 type Thing.
- Q7243682 type Q12136.
- Q7243682 comment "Primrose syndrome is a rare, slowly progressive genetic disorder that can vary symptomatically between individual cases, but is generally characterised by ossification of the external ears, learning difficulties, and facial abnormalities. It was first described in 1982 in Scotland's Royal National Larbert Institution by Dr D.A.A. Primrose.Primrose syndrome appears to occur spontaneously, regardless of family history. The cause is currently unknown and there are no known treatments.".
- Q7243682 label "Primrose syndrome".
- Q7243682 name "Primrose syndrome".