Clinical Genetics of Polydactyly: An Updated Review

Author:

Umair Muhammad,Ahmad Farooq,Bilal Muhammad,Ahmad Wasim,Alfadhel Majid

Publisher

Frontiers Media SA

Subject

Genetics (clinical),Genetics,Molecular Medicine

Reference61 articles.

1. Mapping of the second locus of postaxial polydactyly type A (PAP-A2) to chromosome 13q21-q32.;Akarsu;Am. J. Hum. Genet.,1997

2. A novel frameshift mutation of the GLI3 gene in a family with broad thumbs with/without big toes, postaxial polydactyly and variable syndactyly of the hands/feet. (Letter).;Al-Qattan;Clin. Genet.,2012

3. Zone of polarizing activity regulatory sequence mutations/duplications with preaxial polydactyly and longitudinal preaxial ray deficiency in the phenotype: a review of human cases, animal models, and insights regarding the pathogenesis.;Al-Qattan;Biomed. Res. Int.,2018

4. “On syndactylies and its association with polydactyly,” in;Bell;The Treasury of Human Inheritance.,1953

5. Preaxial polydactyly of the foot.;Burger;Acta Orthop.,2018

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