A gene ( PEX ) with homologies to endopeptidases is mutated in patients with X-linked hypophosphatemic rickets von Poustka, A, Davies, K.E, Lorenz, B, Korn, B, Drezner, M.K, O'Riordan, J.L.H, Pannetier, S, Rowe, P.S.N, Summerfield, T, Nesbitt, T, Meindl, A, Lehrach, H, Strom, T.M, Popowska, E, Mountford, R, Cagnoli, B, Mohnike, K.L, Hanauer, A, Reinhardt, R, Read, A.P, Econs, M.J, Murken, J, de Jong, P, Goulding, J.N, Hennig, S, Meitinger, T, Oudet, C, Francis, F, Pronicka, E

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Using case study comparisons to explore genotype-phenotype correlations in Williams-Beuren syndrome von Karmiloff-Smith, A, Grant, J, Ewing, S, Carette, M J, Metcalfe, K, Donnai, D, Read, A P, Tassabehji, M

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Coinheritance of two rare genodermatoses (Papillon–Lefèvre syndrome and oculocutaneous albinism type 1) in two families: a genetic study von Hewitt, C., Wu, C‐L., Hattab, F.N., Amin, W., Ghaffar, K.A., Toomes, C., Sloan, P., Read, A.P., James, J.A., Thakker, N.S.

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Waardenburg Syndrome von Read, A.P.

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The Genetics of Otosclerosis: Pedigree Studies and Linkage Analysis von Saeed, S.R., Briggs, M., Lobo, C., Al-Zoubi, F., Ramsden, R.T., Read, A.P.

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Hypomelanosis of Ito von Donnai, Dian, Read, A.P.

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Apparent prevention of neural tube defects by periconceptional vitamin supplementation von Smithells, R W, Sheppard, S, Schorah, C J, Seller, M J, Nevin, N C, Harris, R, Read, A P, Fielding, D W

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DIPLOID/TRIPLOID MIXOPLOIDY AND HYPOMELANOSIS OF ITO von Donnai, Dian, Mckeown, Carole, Andrews, Tony, Read, A.P.

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FURTHER EXPERIENCE OF VITAMIN SUPPLEMENTATION FOR PREVENTION OF NEURAL TUBE DEFECT RECURRENCES von Smithells, R.W., Seller, M.J., Harris, R., Fielding, D.W., Schorah, C.J., Nevin, N.C., Sheppard, S., Read, A.P., Walker, S., Wild, J.

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Genetics von Read, A.P.

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Linkage analysis of two cloned DNA sequences, DXS197 and DXS207, in hypophosphatemic rickets families von Thakker, R.V., Davies, K.E., Read, A.P., Tippett, P., Wooding, C., Flint, T., Woob, S., Kruse, T.A., Whyte, M.P., O'Riordan, J.L.H.

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CLINIC EXPERIENCE OF PRENATAL DIAGNOSIS OF CYSTIC FIBROSIS BY USE OF LINKED DNA PROBES von Super, Maurice, Schwarz, M., Elles, R.G., Ivinson, A., Giles, L., Read, A.P., Harris, R.

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Genetics: By Ursula Goodenough. 2nd Edition. Philadelphia, London and Toronto: W. B. Saunders, 1978, pp. 840, price £7.50 von Read, A.P.

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DNA PROBES IN DIFFERENTIAL DIAGNOSIS OF BECKER MUSCULAR DYSTROPHY AND SPINAL MUSCULAR ATROPHY von Lunt, P.W., Cumming, W.J.K., Kingston, H., Read, A.P., Mountford, R.C., Mahon, M., Harris, R.

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5. Chromosomal localisation of DNA probes for the hypophosphataemic rickets gene von Rowe, P.S.N., Benham, Frances, Read, A.P., Thakker, R.V., Kruse, T., Camarino, Giovanna, Davies, Kay E, O'Riordan, J.L.H.

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EFFECTIVE STRATEGY FOR PRENATAL PREDICTION OF DUCHENNE AND BECKER MUSCULAR DYSTROPHY von Forrest, S.M., Cross, G.S., Thomas, N.S.T., Harper, P.S., Smith, T.J., Read, A.P., Mountford, R.C., Geirsson, R.T., Davies, K.E.

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Gene linkage and genetic deafness von Cremers, C.W.R.J., Brown, S.D.M., Steel, K.P., Brunner, H.G., Read, A.P., Kimberling, W.J.

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DECLINING INCIDENCE OF NEURAL TUBE DEFECTS von Harris, Rodney, Read, A.P.

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X-linked and FSH dystrophies in one family von Lecky, B.R.F., MacKenzie, J.M., Read, A.P., Wilcox, D.E.

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POSSIBLE MATERNAL EFFECT IN GENETIC SUSCEPTIBILITY TO MYASTHENIA GRAVIS von Read, A.P., Kerzin-Storrar, Lauren, Dyer, P.A., Metcalfe, R.A.

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