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By Aliferis K.   Marsal C.   Pelletier V.   Doray B.   Weiss M.M.   Tops C.M.J.   Speeg-Schatz C.   Lesnik S.A.J.   Dollfus H.  

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Congenital Hypothyroidism in Peters Plus Syndrome

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Screening of the USH1G Gene among Spanish Patients with Usher Syndrome. Lack of Mutations and Evidence of a Minor Role in the Pathogenesis of the Syndrome

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Molecular Analysis of the CYP1B1 Gene: Identification of Novel Truncating Mutations in Patients with Primary Congenital Glaucoma

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