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ARVO Annual Meeting Abstract March 2012

FYCO1 Mutation Hotspot in Congenital Cataract

Hana Abouzeid; Gihan Helmy; Mohamed El Sada; Mai Sherif; Mariam H. Yacoub; Gaelle Boisset; Tatiana Favez; Daniel F. Schorderet

Invest. Ophthalmol. Vis. Sci.. 2012; 53(14):1723. doi:

ARVO Annual Meeting Abstract April 2011

A New Locus On Chromosome 14 Causes Waardenburg Anophthalmia Syndrome

Hana Abouzeid; Gaelle Boisset; Tatiana Favez; Mohamed A. Youssef; Iman Marzouk; Nihal ElShakankiri; Nader Bayoumi; Céline Agosti; Francis L. Munier; Daniel F. Schorderet

Invest. Ophthalmol. Vis. Sci.. 2011; 52(14):67. doi:

ARVO Annual Meeting Abstract May 2007

Pip5k3 Fleck Corneal Dystrophy-Linked Gene Characterization in Zebrafish

G. Boisset; B. K. Polok; D. F. Schorderet

Invest. Ophthalmol. Vis. Sci.. 2007; 48(13):5699. doi:

ARVO Annual Meeting Abstract May 2006

Knockdown of PIP5k3 Fleck Corneal Dystrophy–Linked Gene in Zebrafish

G. Boisset; A. Tasinato; S. Métrailler; D.F. Schorderet

Invest. Ophthalmol. Vis. Sci.. 2006; 47(13):2777. doi:

ARVO Annual Meeting Abstract May 2006

Biological Characterization of Gene Response in Rpe65–/– Mouse Model of Leber's Congenital Amaurosis During Progression of the Disease

S. Cottet; L. Michaut; G. Boisset; Y. Arsenijevic; U. Schlecht; F.L. Munier; W. Gehring; D.F. Schorderet

Invest. Ophthalmol. Vis. Sci.. 2006; 47(13):4560. doi:

ARVO Annual Meeting Abstract May 2006

Altered Expression of Anti– and Pro–Apoptotic Genes in Rpe65–/– Mouse Model of Leber's Congenital Amaurosis

D.F. Schorderet; G. Boisset; T. Favez; S. Cottet

Invest. Ophthalmol. Vis. Sci.. 2006; 47(13):4598. doi:

ARVO Annual Meeting Abstract May 2005

An Additional Locus for Autosomal Dominant Retinitis Pigmentosa (RP) on Chromosome 7p

G. Boisset; L. Tiab; S. Bolay; T. Delarive; S. Métrailler; M. Matter; M.–C. Gaillard; F.X. Borruat; F. Munier; D.F. Schorderet

Invest. Ophthalmol. Vis. Sci.. 2005; 46(13):511. doi:

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