"Hélène Dollfus" appeared in Books and Chapters

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"Hélène Dollfus" appeared in Books and Chapters

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Chapter	Author(s)	Book	Book Authors	Year	Publisher
3 Bardet-Biedl Syndrome: New Insights into Ciliopathies and Oligogenic Traits	Hélène Dollfus; Philip Beales; Nicholas Katsanis	Obesity: Genomics and Postgenomics	Karine Clement; Thorkild I. A. Sorensen	2008	Routledge
Disease-Associated Variants of the Rod-derived Cone Viability Factor (RdCVF) in Leber Congenital Amaurosis	Sylvain Hanein; Isabelle Perrault; Sylvie Gerber; Hélène Dollfus; Jean-Louis Dufier; Josué Feingold et al.	Retinal Degenerative Diseases	Joe G. Hollyfield; Robert E. Anderson; Matthew M. LaVail	2006	Springer US
Description of Two Siblings with Apparently Severe CEP290 Mutations and Unusually Mild Retinal Disease Unrelated to Basal Exon Skipping or Nonsense-Associated Altered Splicing	Iris Barny; Isabelle Perrault; Marlène Rio; Hélène Dollfus; Sabine Defoort-Dhellemmes; Josseline Kaplan et al.	Retinal Degenerative Diseases: Mechanisms and Experimental Therapy	Catherine Bowes Rickman; Christian Grimm; Robert E. Anderson; John D. Ash; Matthew M. LaVail; Joe G. Hollyfield	1st ed. 2019	Springer International Publishing
Clinical and Genetic Heterogeneity of Leber’s Congenital Amaurosis	Hélène Dollfus; Jean-Michal Rozet; Oliver Delrieu; Alain Vignal; Imhad Ghazi; Jean-Louis Dufier et al.	Retinal Degeneration: Clinical and Laboratory Applications	Robert E. Anderson; Joe G. Hollyfield; Matthew M. LaVail	1993	Springer US
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