Literature DB >> 1059061

Orofaciodigital syndrome, type I: a phenotypic and genetic analysis.

M Melnick, E D Shields.   

Abstract

An additional family with the orofaciodigital syndrome. Type I, is presented. On the basis of previously published pedigrees, as well as the present case, data are presented that conclusively support an X-linked dominant mode of inheritance. Segregation analysis demonstrated that not only is there lethality in the male but there is significant lethality in the female due to lyonization. In addition, a review of the familial cases will demonstrate a large degree of intra- and interfamilial variation.

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Year:  1975        PMID: 1059061     DOI: 10.1016/0030-4220(75)90370-9

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


  2 in total

1.  Mohr-Claussen Syndrome: A Rare Case.

Authors:  Manjiri Uttam Joshi; Namish Jagdish Chandra Batra; Ankita Pradeep Patel
Journal:  J Clin Diagn Res       Date:  2016-10-01

2.  X-linked dominant inherited diseases with lethality in hemizygous males.

Authors:  R Wettke-Schäfer; G Kantner
Journal:  Hum Genet       Date:  1983       Impact factor: 4.132

  2 in total

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