Literature DB >> 5971712

[Contribution to the study of the heredity of epibulbar dermoids].

F Proto, L Scullica.   

Abstract

Mesh：

Year:  1966        PMID： 5971712     DOI： 10.1017/s1120962300014943

Source DB:  PubMed          Journal:  Acta Genet Med Gemellol (Roma)        ISSN： 0001-5660


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  4 in total

1.  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

2.  Empirical recurrence risk after unidentified multiple congenital abnormalities.

Authors:  A Czeizel; J Métneki
Journal:  J Med Genet       Date:  1983-10       Impact factor: 6.318

3.  A Lebanese family with autosomal recessive oculo-auriculo-vertebral (OAV) spectrum and review of the literature: is OAV a genetically heterogeneous disorder?

Authors:  Chantal Farra; Khaled Yunis; Nadine Yazbeck; Marianne Majdalani; Lama Charafeddine; Rima Wakim; Johnny Awwad
Journal:  Appl Clin Genet       Date:  2011-07-06

4.  Goldenhar Syndrome: A rare case report.

Authors:  Ruchi Bhuyan; Abhishek Ranjan Pati; Sanat Kumar Bhuyan; Bikash Bishwadarshee Nayak
Journal:  J Oral Maxillofac Pathol       Date:  2016 May-Aug
  4 in total

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