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Academic Journal

Diagnostic exome sequencing in 266 Dutch patients with visual impairment

Subjects: RETINITIS-PIGMENTOSA; CONGENITAL CATARACT; EYE DISEASE

  • Source: Haer-Wigman, L, van Zelst-Stams, W A G, Pfundt, R, van den Born, L I, Klaver, C C W, Verheij, J B G M, Hoyng, C B, Breuning, M H, Boon, C J F, Kievit, A J, Verhoeven, V J M, Pott, J W R, Sallevelt, S

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Academic Journal

Diagnostic exome sequencing in 266 Dutch patients with visual impairment

Subjects: RETINITIS-PIGMENTOSA; CONGENITAL CATARACT; EYE DISEASE

  • Source: Haer-Wigman, L, van Zelst-Stams, W A G, Pfundt, R, van den Born, L I, Klaver, C C W, Verheij, J B G M, Hoyng, C B, Breuning, M H, Boon, C J F, Kievit, A J, Verhoeven, V J M, Pott, J W R, Sallevelt, S

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Academic Journal

Genetic analysis and clinical phenotype of two Indian families with X-linked choroideremia

Subjects: Choroideremia gene; genetic analysis; next generation sequencing

  • Source: Battu, R, Jeyabalan, N, Murthy, P, Reddy, K S, Schouten, J & Webers, C 2016, 'Genetic analysis and clinical phenotype of two Indian families with X-linked choroideremia', Indian Journal of

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Academic Journal

Genetic analysis and clinical phenotype of two Indian families with X-linked choroideremia

Subjects: Choroideremia gene; genetic analysis; next generation sequencing

  • Source: Battu, R, Jeyabalan, N, Murthy, P, Reddy, K S, Schouten, J & Webers, C 2016, 'Genetic analysis and clinical phenotype of two Indian families with X-linked choroideremia', Indian Journal of

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  • 1-4 ل  4 نتائج ل ""Retinal Dystrophies""