Literature DB >> 15205255

Vitreoretinal abnormalities in the Conradi-Hunermann form of chondrodysplasia punctata.

Y D Ramkissoon, E J Mayer, C Gibbon, R J Haynes.   

Abstract

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Year:  2004        PMID: 15205255      PMCID: PMC1772228          DOI: 10.1136/bjo.2003.038638

Source DB:  PubMed          Journal:  Br J Ophthalmol        ISSN: 0007-1161            Impact factor:   4.638


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  7 in total

Review 1.  Molecular genetics of rhegmatogenous retinal detachment.

Authors:  A J Richards; J D Scott; M P Snead
Journal:  Eye (Lond)       Date:  2002-07       Impact factor: 3.775

2.  Conradi-Hünermann syndrome with ocular anomalies.

Authors:  Y Tanaka; A Saitoh; H Taniguchi; K Oba; T Kitaoka; T Amemiya
Journal:  Ophthalmic Genet       Date:  1999-12       Impact factor: 1.803

3.  Heterogeneity of Chondrodysplasia punctata.

Authors:  J W Spranger; J M Opitz; U Bidder
Journal:  Humangenetik       Date:  1971

4.  Ocular manifestations of Conradi disease.

Authors:  J Y Massey; F H Roy
Journal:  Arch Ophthalmol       Date:  1974-12

5.  Clinical and genetic aspects of Conradi-Hünermann disease. A report of three familial cases and review of the literature.

Authors:  M C Silengo; L Luzzatti; F N Silverman
Journal:  J Pediatr       Date:  1980-12       Impact factor: 4.406

6.  Chondrodysplasia punctata-23 cases of a mild and relatively common variety.

Authors:  L J Sheffield; D M Danks; V Mayne; A L Hutchinson
Journal:  J Pediatr       Date:  1976-12       Impact factor: 4.406

7.  Cataracts as a marker of genetic heterogeneity in chondrodysplasia punctata.

Authors:  R Happle
Journal:  Clin Genet       Date:  1981-01       Impact factor: 4.438

  7 in total
  1 in total

1.  Specific entities affecting the craniocervical region: syndromes affecting the craniocervical junction.

Authors:  Arnold H Menezes; Timothy W Vogel
Journal:  Childs Nerv Syst       Date:  2008-03-28       Impact factor: 1.475

  1 in total

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