X-Linked Retinoschisis: Novel Clinical Observations and Genetic Spectrum in 340 Patients von Hahn, Leo C, van Schooneveld, Mary J, Wesseling, Nieneke L, Florijn, Ralph J, Ten Brink, Jacoline B, Lissenberg-Witte, Birgit I, Strubbe, Ine, Meester-Smoor, Magda A, Thiadens, Alberta A, Diederen, Roselie M, van Cauwenbergh, Caroline, de Zaeytijd, Julie, Walraedt, Sophie, de Baere, Elfride, Klaver, Caroline C W, Ossewaarde-van Norel, Jeannette, van den Born, L Ingeborgh, Hoyng, Carel B, van Genderen, Maria M, Sieving, Paul A, Leroy, Bart P, Bergen, Arthur A, Boon, Camiel J F

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Macular Dystrophy and Cone-Rod Dystrophy Caused by Mutations in the RP1 Gene: Extending the RP1 Disease Spectrum von Verbakel, Sanne K, van Huet, Ramon A C, den Hollander, Anneke I, Geerlings, Maartje J, Kersten, Eveline, Klevering, B Jeroen, Klaver, Caroline C W, Plomp, Astrid S, Wesseling, Nieneke L, Bergen, Arthur A B, Nikopoulos, Konstantinos, Rivolta, Carlo, Ikeda, Yasuhiro, Sonoda, Koh-Hei, Wada, Yuko, Boon, Camiel J F, Nakazawa, Toru, Hoyng, Carel B, Nishiguchi, Koji M

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The Natural History of Leber Congenital Amaurosis and Cone–Rod Dystrophy Associated with Variants in the GUCY2D Gene von Hahn, Leo C., Georgiou, Michalis, Almushattat, Hind, van Schooneveld, Mary J., de Carvalho, Emanuel R., Wesseling, Nieneke L., ten Brink, Jacoline B., Florijn, Ralph J., Lissenberg-Witte, Birgit I., Strubbe, Ine, van Cauwenbergh, Caroline, de Zaeytijd, Julie, Walraedt, Sophie, de Baere, Elfride, Mukherjee, Rajarshi, McKibbin, Martin, Meester-Smoor, Magda A., Thiadens, Alberta A.H.J., Al-Khuzaei, Saoud, Akyol, Engin, Lotery, Andrew J., van Genderen, Maria M., Ossewaarde-van Norel, Jeannette, van den Born, L. Ingeborgh, Hoyng, Carel B., Klaver, Caroline C.W., Downes, Susan M., Bergen, Arthur A., Leroy, Bart P., Michaelides, Michel, Boon, Camiel J.F.

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X-Linked Retinoschisis von Hahn, Leo C., van Schooneveld, Mary J., Wesseling, Nieneke L., Florijn, Ralph J., ten Brink, Jacoline B., Lissenberg-Witte, Birgit I., Strubbe, Ine, Meester-Smoor, Magda A., Thiadens, Alberta A., Diederen, Roselie M., van Cauwenbergh, Caroline, de Zaeytijd, Julie, Walraedt, Sophie, de Baere, Elfride, Klaver, Caroline C.W., Ossewaarde-van Norel, Jeannette, van den Born, L. Ingeborgh, Hoyng, Carel B., van Genderen, Maria M., Sieving, Paul A., Leroy, Bart P., Bergen, Arthur A., Boon, Camiel J.F.

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X-Linked Retinoschisis: Novel Clinical Observations and Genetic Spectrum in 340 Patients von Hahn, Leo C, van Schooneveld, Mary J, Wesseling, Nieneke L, Florijn, Ralph J, ten Brink, Jacoline B, Lissenberg-Witte, Birgit I, Strubbe, Ine, Meester-Smoor, Magda A, Thiadens, Alberta A, Diederen, Roselie M, van Cauwenbergh, Caroline, de Zaeytijd, Julie, Walraedt, Sophie, de Baere, Elfride, Klaver, Caroline C.W, Ossewaarde-van Norel, Jeannette, Ingeborgh van den Born, L, Hoyng, Carel B, van Genderen, Maria M, Sieving, Paul A, Leroy, Bart P, Bergen, Arthur A, Boon, Camiel J.F

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X-linked Retinoschisis : novel clinical observations and genetic spectrum in 340 patients von Hahn, Leo C, Schooneveld, Mary J. van, Wesseling, Nieneke L, Florijn, Ralph J, Brink, Jacoline B. ten, Lissenberg-Witte, Birgit I, Strubbe, Ine, Meester-Smoor, Magda A, Thiadens, Alberta A, Diederen, Roselie M, Van Cauwenbergh, Caroline, De Zaeytijd, Julie, WALRAEDT, SOPHIE, De Baere, Elfride, Klaver, Caroline C. W, Norel, Jeannette Ossewaarde-van, Born, L. Ingeborgh van den, Hoyng, Carel B, Genderen, Maria M. van, Sieving, Paul A, Leroy, Bart, Bergen, Arthur A, Boon, Camiel

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The natural history of leber congenital amaurosis and cone–rod dystrophy associated with variants in the GUCY2D gene von Hahn, Leo C, Georgiou, Michalis, Almushattat, Hind, van Schooneveld, Mary J, de Carvalho, Emanuel R, Wesseling, Nieneke L, ten Brink, Jacoline B, Florijn, Ralph J, Lissenberg-Witte, Birgit I, Strubbe, Ine, Van Cauwenbergh, Caroline, De Zaeytijd, Julie, WALRAEDT, SOPHIE, De Baere, Elfride, Mukherjee, Rajarshi, McKibbin, Martin, Meester-Smoor, Magda A, Thiadens, Alberta A.H.J, Al-Khuzaei, Saoud, Akyol, Engin, Lotery, Andrew J, van Genderen, Maria M, Ossewaarde-van Norel, Jeannette, van den Born, L. Ingeborgh, Hoyng, Carel B, Klaver, Caroline C.W, Downes, Susan M, Bergen, Arthur A, Leroy, Bart, Michaelides, Michel, Boon, Camiel J.F

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The Natural History of Leber Congenital Amaurosis and Cone-Rod Dystrophy Associated with Variants in the GUCY2D Gene von Hahn, Leo C, Georgiou, Michalis, Almushattat, Hind, van Schooneveld, Mary J, de Carvalho, Emanuel R, Wesseling, Nieneke L, Ten Brink, Jacoline B, Florijn, Ralph J, Lissenberg-Witte, Birgit I, Strubbe, Ine, van Cauwenbergh, Caroline, de Zaeytijd, Julie, Walraedt, Sophie, de Baere, Elfride, Mukherjee, Rajarshi, McKibbin, Martin, Meester-Smoor, Magda A, Thiadens, Alberta AHJ, Al-Khuzaei, Saoud, Akyol, Engin, Lotery, Andrew J, van Genderen, Maria M, Norel, Jeannette Ossewaarde-van, Ingeborgh van den Born, L, Hoyng, Carel B, Klaver, Caroline CW, Downes, Susan M, Bergen, Arthur A, Leroy, Bart P, Michaelides, Michel, Boon, Camiel JF

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