Literature DB >> 1057128

Oculodento-osseous dysplasia syndrome.

G A Zach.   

Abstract

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Mesh：

Year:  1975        PMID： 1057128     DOI： 10.1016/0030-4220(75)90354-0

Source DB:  PubMed          Journal:  Oral Surg Oral Med Oral Pathol        ISSN： 0030-4220


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  3 in total

Review 1.  Gap junctions in inherited human disorders of the central nervous system.

Authors:  Charles K Abrams; Steven S Scherer
Journal:  Biochim Biophys Acta       Date:  2011-08-16

2.  Connexin 43 (GJA1) mutations cause the pleiotropic phenotype of oculodentodigital dysplasia.

Authors:  William A Paznekas; Simeon A Boyadjiev; Robert E Shapiro; Otto Daniels; Bernd Wollnik; Catherine E Keegan; Jeffrey W Innis; Mary Beth Dinulos; Cathy Christian; Mark C Hannibal; Ethylin Wang Jabs
Journal:  Am J Hum Genet       Date:  2002-11-27       Impact factor: 11.025

Review 3.  Genetics of microphthalmos.

Authors:  M Warburg
Journal:  Int Ophthalmol       Date:  1981-08       Impact factor: 2.031
  3 in total

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