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.

Volltext

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.

Volltext

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.

Volltext

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

Volltext

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

Volltext

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.

Volltext

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

Volltext

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

Volltext

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

Volltext

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

Volltext

Prenatal exclusion testing for Huntington's disease: a problem of too much information von Millan, F A, Curtis, A, Mennie, M, Holloway, S, Boxer, M, Faed, M J, Crawford, J W, Liston, W A, Brock, D J

Volltext

INHERITED PERICENTRIC INVERSION OF CHROMOSOME 5: A FAMILY WITH HISTORY OF NEONATAL DEATH AND A CASE OF THE “CRI DU CHAT” SYNDROME von Faed, M J. W, Marrian, V J, Robertson, J, Robson, E B, Cook, P J. L

Volltext

Features of di George syndrome in a child with 45,XX,-3,-22,+der(3),t(3;22)(p25;q11) von Faed, M J, Robertson, J, Beck, J S, Cater, J I, Bose, B, Madlom, M M

Volltext

Wiedemann-Beckwith syndrome in one of monozygotic twins von Bose, B, Wilkie, R A, Madlom, M, Forsyth, J S, Faed, M J

Volltext

Nucleolus organiser regions on mitotic and meiotic chromosomes from infertile males investigated using a specific silver stain von Ironside, J, Faed, M J

Volltext

Chromosome abnormality in couples with histories of multiple abortions. The outcome of pregnancies subsequent to ascertainment and a study of familial translocation carriers von Wolstenholme, J, Faed, M J, Robertson, J, Lamont, M A

Volltext

Sister chromatid exchange and chromosome aberration rates in a group of psoriatics before and after a course of PUVA treatment von FAED, M. J. W., WILLIAMSON, L., PETERSON, S., LAKSHMIPATHI, T., JOHNSON, B. E., FRAIN-BELL, W.

Volltext

The effect of 8-methoxypsoralen and longwave UV-radiation on growth rates of human epidermal cells in culture von West, M. R., Faed, M. J. W.

Volltext

Sister chromatid exchanges in human lymphocytes exposed to 8-methoxypsoralen and long wave UV radiation prior to incorporation of bromodeoxyuridine von Mourelatos, D., Faed, M. J. W., Johnson, B. E.

Volltext

THE FETAL MANIFESTATIONS OF THE 45XO KARYOTYPE von Rushton, D. I., Faed, M. J. W., Richards, Susan E. M., Bain, A. D.

Volltext