Literature DB >> 5778829

A new familial syndrome of oral, cranial, and digital anomalies.

R C Juberg, J R Hayward.   

Abstract

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Year:  1969        PMID： 5778829     DOI： 10.1016/s0022-3476(69)80138-1

Source DB:  PubMed          Journal:  J Pediatr        ISSN： 0022-3476            Impact factor:   4.406


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  5 in total

1.  Popliteal pterygium syndrome.

Authors:  U G Froster-Iskenius
Journal:  J Med Genet       Date:  1990-05       Impact factor: 6.318

Review 2.  The orocraniodigital syndrome of Juberg and Hayward.

Authors:  A Verloes; M Le Merrer; J C Davin; P Wittamer; C Abrassart; G Bricteux; M L Briard
Journal:  J Med Genet       Date:  1992-04       Impact factor: 6.318

3.  A case of the orocraniodigital (Juberg-Hayward) syndrome.

Authors:  N C Nevin; P Henry; P T Thomas
Journal:  J Med Genet       Date:  1981-12       Impact factor: 6.318

4.  Autosomal dominant asymmetrical radial dysplasia, dysmorphic facies, and conductive hearing loss (facioauriculoradial dysplasia).

Authors:  A E Harding; C M Hall; M Baraitser
Journal:  J Med Genet       Date:  1982-04       Impact factor: 6.318

5.  Orocraniodigital (Juberg-Hayward) syndrome with growth hormone deficiency.

Authors:  H M Kingston; I A Hughes; P S Harper
Journal:  Arch Dis Child       Date:  1982-10       Impact factor: 3.791
  5 in total

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