Bardet–Biedl syndrome-Reference-Cited by-同舟云学术

Bardet–Biedl syndrome

Published:2012-06-20 Issue:1 Volume:21 Page:8-13
ISSN:1018-4813
Container-title:European Journal of Human Genetics
language:en
Short-container-title:Eur J Hum Genet

Author:

Forsythe Elizabeth,Beales Philip L

Publisher

Springer Science and Business Media LLC

Subject

Genetics(clinical),Genetics

Link

http://www.nature.com/articles/ejhg2012115.pdf

Reference62 articles.

1. Laurence JZ, Moon RC : Four cases of ‘retinitis pigmentosa’ occurring in the same family, and accompanied by general imperfections of development. Obes Res 1995; 3: 400–403.

2. Bardet G : On congenital obesity syndrome with polydactyly and retinitis pigmentosa (a contribution to the study of clinical forms of hypophyseal obesity). Obes Res 1995; 3: 387–399.

3. Biedl A : A pair of siblings with adiposo-genital dystrophy. Obes Res 1995; 3: 404.

4. Beales PL, Elcioglu N, Woolf AS, Parker D, Flinter FA : New criteria for improved diagnosis of Bardet–Biedl syndrome: results of a population survey. J Med Genet 1999; 36: 437–446.

5. Waters AM, Beales PL : Bardet–Biedl Syndrome; GeneReviews [Internet] 1993-2003 (Updated 2011).

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