Fragile X syndrome von McKinley, M J, Nicolaides, K H, Kearney, L U, Heron, O

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Prenatal diagnosis of fragile X syndrome by placental (chorionic villi) biopsy culture von McKinley, Mark J., Kearney, Lyndal U., Nicolaides, Kypros H., Gosden, Christine M., Webb, Tessa P., Fryns, Jean P.

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Mosaic trisomy 7 confined to the placenta von McKinley, Mark J., Kearney, Lyndal U., Nicolaides, Kypros H., Rosevear, Sylvia K., Bradley, Robert, Heron, Oonagh, Gosden, Christine M., Neri, Giovanni, Reynolds, James F.

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Molecular cytogenetic delineation of the critical deleted region in the 5q− syndrome von Jaju, Rina J., Boultwood, Jacqueline, Oliver, Fiona J., Kostrzewa, Markus, Fidler, Carrie, Parker, Norman, McPherson, John D., Morris, Stephan W., Müller, Ulrich, Wainscoat, James S., Kearney, Lyndal

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A new recurrent translocation, t(5;11)(q35;p15.5), associated with del(5q) in childhood acute myeloid leukemia von JAJU, R. J, HAAS, O. A, MORRIS, S. W, WAINSCOAT, J. S, KEARNEY, L, NEAT, M, HARBOTT, J, SAHA, V, BOULTWOOD, J, BROWN, J. M, PIRC-DANOEWINATA, H, KRINGS, B. W, MÜLLER, U

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