Epigenetics – an introductory overview von Ramesar, R.S.

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Spondyloepimetaphyseal dysplasia with joint laxity (Beighton type); mutation analysis in eight affected South African families von Vorster, A.A., Beighton, P., Ramesar, R.S.

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Diagnisis - digitotalar dysmorphism - molecular elucidation : in practice von Vorster, A.A., Ramesar, R.S., Beighton, P.

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Digitotalar dysmorphism: Molecular elucidation von Vorster, Anna Alvera, Beighton, Peter, Ramesar, Rajkumar Sewcharan

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Inherited retinal disorders in South Africa and the clinical impact of evolving technologies : how human genetics came to SA von Bardien, S., Loubser, F., Bartmann, L., Rebello, G., Roberts, L., Ramesar, R.S., September, A.V., Bardien, S., Greenberg, L.J., Goliath, R.

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The value of genetic testing for inherited retinal disease caused by mutations in the ABCA4 gene in South Africans : correspondence von Ramesar, R.S., Roberts, L.J., Goolam Hoosen, T., Hardie, S., Greenberg, L.J.

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Strengthening human genetics research in Africa: report of the 9th meeting of the African Society of Human Genetics in Dakar in May 2016 von Ndiaye Diallo, R., Gadji, M., Hennig, B. J., Guèye, M. V., Gaye, A., Diop, J. P. D., Sylla Niang, M., Lopez Sall, P., Guèye, P. M., Dem, A., Faye, O., Dieye, A., Cisse, A., Sembene, M., Ka, S., Diop, N., Williams, S. M., Matovu, E., Ramesar, R.S., Wonkam, A., Newport, M., Rotimi, C., Ramsay, M.

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The value of genetic testing for inherited retinal disease caused by mutations in the ABCA4 gene in South Africans von Roberts, L J, Hardie, S, Gollam Hoosen, T, Ramesar, R S, Greenberg, L J

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A computer-based register for inherited retinal dystrophies in Southern Africa von Rebello, M.T., Greenberg, L.J., Ramesar, R.S.

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X-linked ocular albinism and sensorineural deafness: Linkage to Xp22. 3 von Winship, I.M., Babaya, M., Ramesar, R.S.

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Whole-Exome Sequencing Identifies Biallelic IDH3A Variants as a Cause of Retinitis Pigmentosa Accompanied by Pseudocoloboma von Pierrache, L.H.M., Kimchi, A., Ratnapriya, R., Roberts, L., Astuti, G.D.N., Obolensky, A., Beryozkin, A., Tjon-Fo-Sang, M.J.H., Schuil, J., Klaver, C.C.W., Bongers, E.M.H.F., Haer-Wigman, L., Schalij, N., Breuning, M.H., Fischer, G.M., Banin, E., Ramesar, R.S., Swaroop, A., Born, L.I. van den, Sharon, D., Cremers, F.P.M.

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Stickler-like syndrome due to a dominant negative mutation in the COL2A1 gene von Ballo, R., Beighton, P.H., Ramesar, R.S.

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Obesity, Aspirin, and Risk of Colorectal Cancer in Carriers of Hereditary Colorectal Cancer: A Prospective Investigation in the CAPP2 Study von Movahedi, M., Bishop, D.T., Macrae, F., Mecklin, J.P., Moeslein, G., Olschwang, S., Eccles, D., Evans, D.G., Maher, E.R., Bertario, L., Bisgaard, M.L., Dunlop, M.G., Ho, J.W., Hodgson, S.V., Lindblom, A., Lubinski, J., Morrison, P.J., Murday, V., Ramesar, R.S., Side, L., Scott, R.J., Thomas, H.J.W., Vasen, H.F., Burn, J., Mathers, J.C.

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Stickler‐like syndrome due to a dominant negative mutation in the COL2A1 gene von Ballo, R., Beighton, P.H., Ramesar, R.S.

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