Literature DB >> 4368935

Mulibrey nanism; an inherited dysmorphic syndrome with characteristic ocular findings.

C Raitta, J Perheentupa.   

Abstract

Mesh：

Year:  1974        PMID： 4368935

Source DB:  PubMed          Journal:  Acta Ophthalmol Suppl        ISSN： 0065-1451


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  2 in total

Review 1.  The Finnish Disease Heritage III: the individual diseases.

Authors:  Reijo Norio
Journal:  Hum Genet       Date:  2003-03-08       Impact factor: 4.132

2.  Mulibrey nanism: clinical features and diagnostic criteria.

Authors:  N Karlberg; H Jalanko; J Perheentupa; M Lipsanen-Nyman
Journal:  J Med Genet       Date:  2004-02       Impact factor: 6.318
  2 in total

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