Showing 1 - 5 results of 5 for search 'Dumanski, J', query time: 0.07s
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Molecular characterization of a 130-kb terminal microdeletion at 22q in a child with mild mental retardation. by Wong, A, Ning, Y, Flint, J, Clark, K, Dumanski, J, Ledbetter, D, McDermid, H
Published 1997Journal article -
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Molecular genetic study of the frequency of monosomy 22q11 in DiGeorge syndrome. by Carey, A, Kelly, D, Halford, S, Wadey, R, Wilson, D, Goodship, J, Burn, J, Paul, T, Sharkey, A, Dumanski, J
Published 1992Journal article -
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PRR14L mutations are associated with chromosome 22 acquired uniparental disomy, age-related clonal hematopoiesis and myeloid neoplasia by Chase, A, Pellagatti, A, Singh, S, Score, J, Tapper, W, Lin, F, Hoade, Y, Bryant, C, Trim, N, Yip, B, Zoi, K, Rasi, C, Forsberg, L, Dumanski, J, Boultwood, J, Cross, N
Published 2018Journal article -
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Mosaic loss of chromosome Y in blood is associated with Alzheimer disease by Dumanski, J, Lambert, J, Rasi, C, Giedraitis, V, Davies, H, Grenier-Boley, B, Lindgren, C, Campion, D, Dufouil, C, Pasquier, F, Amouyel, P, Lannfelt, L, Ingelsson, M, Kilander, L, Lind, L, Forsberg, L
Published 2016Journal article