The molecular genetics of Bardet–Biedl syndrome-Reference-Cited by-同舟云学术

The molecular genetics of Bardet–Biedl syndrome

Published:2001-06-01 Issue:3 Volume:11 Page:317-321
ISSN:0959-437X
Container-title:Current Opinion in Genetics & Development
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Author:

Sheffield V

Publisher

Elsevier BV

Subject

Developmental Biology,Genetics

Reference47 articles.

1. Four cases of retinitis pigmentosa occurring in the same family and accompanied by general imperfection of development;Laurence;Ophthalmic Rev,1866

2. Bardet G: Sur un syndrome d'obesite infantile avec polydactylie et retinite pigmentaire (contribution a l'etude des formes cliniques de l'obesite hypophysaire) [PhD thesis]. Paris, 1920.

3. Ein geschwisterpaar mit adiposo-genitaler dystrophie;Biedl;Deutsch Med Wochenschr,1922

4. Dystrophia adiposogenitalis, with atypical retinitis pigmentosa and mental deficiency, possibly of cerebral origin: a report of four cases in one family;Solis-Cohen;Trans Assoc Am Phys,1924

5. Investigations cliniques et genetiques sur le syndrome de Bardet-Biedl en Suisse;Ammann;J Genet Hum,1970

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