Spectrum of RB1 Mutations in Argentine Patients: 20-years Experience in the Molecular Diagnosis of Retinoblastoma¹

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Molecular characterization of the deletion in retinoblastoma patients with 13q14 cytogenetic anomalies

By Lavanchy Laure   Munier Francis L.   Cousin Pascal   Gaide Anne-Claude   Thonney Francine   Schorderet Daniel F.  

Ophthalmic Genetics, Vol. 22, Iss. 1, 2001-03 ,pp. : 1-10

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Mutational analysis of the RB1 gene in Indian patients with retinoblastoma

By Ata-ur-Rasheed M.   Vemuganti Geeta K.   Honavar Santosh G.   Ahmed Niyaz   Hasnain Seyed E.   Kannabiran Chitra  

Ophthalmic Genetics, Vol. 23, Iss. 2, 2002-06 ,pp. : 121-128

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Mutations in the third exon of the MYOC gene in Spanish patients with primary open angle glaucoma

By Vázquez M. Cabana   Herrero M.V. Olmedo   Bastús M. Baiget   Pérez D. Valverde  

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A possible hot spot in exon 21 of the retinoblastoma gene predisposing to a low penetrant retinoblastoma phenotype?

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