Age-related macular degeneration and the complement system by Khandhadia, S, Cipriani, V, Yates, J.R.W, Lotery, A.J

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Deletions Involving Long-Range Conserved Nongenic Sequences Upstream and Downstream of FOXL2 as a Novel Disease-Causing Mechanism in Blepharophimosis Syndrome by Beysen, D., Raes, J., Leroy, B.P., Lucassen, A., Yates, J.R.W., Clayton-Smith, J., Ilyina, H., Brooks, S. Sklower, Christin-Maitre, S., Fellous, M., Fryns, J.P., Kim, J.R., Lapunzina, P., Lemyre, E., Meire, F., Messiaen, L.M., Oley, C., Splitt, M., Thomson, J., Peer, Y. Van de, Veitia, R.A., De Paepe, A., De Baere, E.

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Tuberous sclerosis presenting in late adult life by Zarei, M, Collins, V P, Chandran, S, Valler, D, Higgins, J N P, Compston, D A S, Yates, J R W

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Familial renal cell carcinoma: clinical and molecular genetic aspects by Maher, ER, Yates, JRW

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Genetic linkage between Von Hippel—Lindau disease and three microsatellite polymorphisms refines the localisation of the VHL locus by Crossey, P.A., Maher, E.R., Jones, M.H., Richards, F.M., Latif, F., Phipps, M.E., Lush, M., Foster, K., Tory, K., Green, J.S., Oostra, B., Yates, J.R.W., Linehan, W.M., Affara, N.A., Lerman, M., Zbar, B., Nakamura, Y., Ferguson-Smith, M.A.

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Deletion of a DNA sequence in eight of nine families with X-linked ichthyosis (steroid sulphatase deficiency) by GILLARD, E. F, AFFARA, N. A, YATES, J. R. W, GOUDIE, D. R, LAMBERT, J, AITKEN, D. A, FERGUSON-SMITH, M. A

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CA repeat polymorphism at the ASS locus by YUILLE, M. A. R, HAMPSON, R. M, HARRIS, R. M, AFFARA, N. A, YATES, J. R. W, FERGUSON-SMITH, M. A

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