Literature DB >> 6794368

The question of hypertelorism in oculodentoosseous dysplasia.

M Fará, R J Gorlin.   

Abstract

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Year:  1981        PMID： 6794368     DOI： 10.1002/ajmg.1320100112

Source DB:  PubMed          Journal:  Am J Med Genet        ISSN： 0148-7299


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  4 in total

1.  Three new cases of oculodentodigital (ODD) syndrome: development of the facial phenotype.

Authors:  M A Patton; K M Laurence
Journal:  J Med Genet       Date:  1985-10       Impact factor: 6.318

Review 2.  Craniotubular bone disorders.

Authors:  R J Gorlin
Journal:  Pediatr Radiol       Date:  1994

3.  Oculodentodigital Syndrome with Syndactyly Type III in a Pakistani consanguineous family.

Authors:  Sumaira Nishat; Qaisar Mansoor; Amara Javaid; Muhammad Ismail
Journal:  J Dermatol Case Rep       Date:  2012-06-30

4.  Oculodentodigital dysplasia and type III syndactyly: separate genetic entities or disease spectrum?

Authors:  L A Brueton; S M Huson; B Farren; R M Winter
Journal:  J Med Genet       Date:  1990-03       Impact factor: 6.318
  4 in total

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