Comparative genomic hybridization analysis of human oocytes and polar bodies von Fragouli, E., Wells, D., Thornhill, A., Serhal, P., Faed, M.J.W., Harper, J.C., Delhanty, J.D.A.

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Acquired dysfibrinogenemia caused by monoclonal production of immunoglobulin lambda light chain von Dear, A, Brennan, S O, Sheat, M J, Faed, J M, George, P M

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Sequential FISH analysis of oocytes and polar bodies reveals aneuploidy mechanisms von Cupisti, S., Conn, C. M., Fragouli, E., Whalley, K., Mills, J. A., Faed, M. J. W., Delhanty, J. D. A.

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Increased susceptibility to maternal aneuploidy demonstrated by comparative genomic hybridization analysis of human MII oocytes and first polar bodies von Fragouli, E., Wells, D., Whalley, K.M., Mills, J.A., Faed, M.J.W., Delhanty, J.D.A.

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Fibrinogen Otago: a major α chain truncation associated with severe hypofibrinogenaemia and recurrent miscarriage von Ridgway, Hayley J., Brennan, Stephen O., Faed, James M., George, Peter M.

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Rapid identification of an A1555G mutation in human mitochondrial DNA implicated in aminoglycoside-induced ototoxicity von Scrimshaw, B. J., Faed, J. M., Tate, W. P., Yun, K.

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Mechanisms of maternal aneuploidy : FISH analysis of oocytes and polar bodies in patients undergoing assisted conception von MAHMOOD, R, BRIERLEY, C. H, FAED, M. J. W, MILLS, J. A, DELHANTY, J. D. A

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Hypofibrinogenemia in an individual with 2 coding (γ82 A→G and Bβ235 P→L) and 2 noncoding mutations von Brennan, Stephen O., Fellowes, Andrew P., Faed, James M., George, Peter M.

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Dietary iron intakes and biochemical iron status of 15-49 year old women in New Zealand: is there a cause for concern? von Ferguson, E L, Morison, I M, Faed, J M, Parnell, W R, McKenzie, J, Wilson, N C, Russell, D G

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Benign FGB (148Lys→Asn, and 448Arg→Lys), and novel causative γ211Tyr→His mutation distinguished by time of flight mass spectrometry in a family with hypofibrinogenaemia von Brennan, Stephen O., Mangos, Hilda, Faed, James M.

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Ascertainment and severity of Marfan syndrome in a Scottish population von Gray, J R, Bridges, A B, Faed, M J, Pringle, T, Baines, P, Dean, J, Boxer, M

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The frequency in New Zealand of a mitochondrial DNA mutation (1555 A to G) associated with aminoglycoside-induced hearing loss von Scrimshaw, B J, Faed, J M, Tate, W P, Yun, K

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Trends in prenatal diagnosis of Down syndrome and other autosomal trisomies in Scotland 1990 to 1994, with associated cytogenetic and epidemiological findings von Carothers, A.D., Boyd, E., Lowther, G., Ellis, P.M., Couzin, D.A., Faed, M.J.W., Robb, A.

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Efficient large-scale screening for the hemochromatosis susceptibility gene mutation von Takeuchi, T, Soejima, H, Faed, J M, Yun, K

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Persistence of two Y chromosomes through meiotic prophase and metaphase I in an XYY man von SPEED, R. M, FAED, M. J. W, BATSTONE, P. J, BARNETSON, W

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BLOOD LEAD, INTELLIGENCE, READING ATTAINMENT, AND BEHAVIOUR IN ELEVEN YEAR OLD CHILDREN IN DUNEDIN, NEW ZEALAND von Silva, Phil A., Hughes, Pauline, Williams, Sheila, Faed, James M.

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Screening for Down's syndrome based on individual risk von Lewis, M, Faed, M J, Howie, P W

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45,X/46,X dic (Y) mosaicism in a phenotypic male von Batstone, P J, Faed, M J, Jung, R T, Gosden, J

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Improved fragile site detection with trimethoprim von MCLEAN, D. A, FAED, M. J. W

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Incidence of familial Hodgkin's disease von Kerzin-Storrar, L, Faed, M J, MacGillivray, J B, Smith, P G

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