Familial insertion (3;5)(q25.3;q22.1q31.3) with deletion or duplication of chromosome region 5q22.1-5q31.3 in ten unbalanced carriers von Arens, Y.H.J.M., Engelen, J.J.M., Govaerts, L.C.P., van Ravenswaay, C.M., Loneus, W.H., van Lent-Albrechts, J.C.M., van der Blij-Philipsen, M., Hamers, A.J.H., Schrander-Stumpel, C.T.R.M.

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Duplication of chromosome region 8p23.1 → p23.3: A benign variant? von Engelen, J.J.M., Moog, U., Evers, J.L.H., Dassen, H., Albrechts, J.C.M., Hamers, A.J.H.

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Deletion of chromosome region 18q21.1 → 18q21.3 in a patient without clinical features of the 18q‐ phenotype von Engelen, J.J.M., Moog, U., Weber, J., Haagen, A.A.M., van Uum, C.M.J., Hamers, A.J.H.

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Intrachromosomal insertion translocation resulting in duplication of chromosome band Yq11.2 in two fertile brothers von Engelen, J.J.M., Arens, Y.H.J.M., Gondrie, E.T.C.M., Alofs, M.G.P., Loneus, W.H., Hamers, A.J.H.

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Characterization of a chromosome 8‐derived minute marker chromosome using microdissection and FISH in a boy with growth retardation von Engelen, J.J.M., Schrander‐Stumpel, C.T.R.M., Theunissen, P.M.V.M., Vaes‐Peeters, G., Albrechts, J.C.M., Hamers, A.J.H.

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De novo duplication (5)(q31.3q33.3): report of a patient and characterization of the duplicated region using microdissection and FISH von Sanchez-Garcia, J.F., de Die-Smulders, C.E.M., Weber, J.W., Jetten, A.G.P., Loneus, W.H., Hamers, A.J.H., Engelen, J.J.M.

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Duplication of chromosome region (16)(p11.2 → p12.1) in a mother and daughter with mild mental retardation von Engelen, J.J.M., de Die‐Smulders, C.E.M., Dirckx, R., Verhoeven, W.M.A., Tuinier, S., Curfs, L.M.G., Hamers, A.J.H.

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Deletion of chromosome region 18q21.1 → 18q21.3 in a patient without clinical features of the 18q- phenotype von Engelen, J.J.M., Moog, U., Weber, J., Haagen, A.A.M., van Uum, C.M.J., Hamers, A.J.H.

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Intrachromosomal insertion translocation resulting in duplication of chromosome band Yq11.2 in two fertile brothers von Engelen, J.J.M., Arens, Y.H.J.M., Gondrie, E.T.C.M., Alofs, M.G.P., Loneus, W.H., Hamers, A.J.H.

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Characterization of a chromosome 8-derived minute marker chromosome using microdissection and FISH in a boy with growth retardation von Engelen, J.J.M., Schrander-Stumpel, C.T.R.M., Theunissen, P.M.V.M., Vaes-Peeters, G., Albrechts, J.C.M., Hamers, A.J.H.

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De novo "pure" partial trisomy (6)(p22.1→pter) in a chromosome 15 with an enlarged satellite, identified by microdissection von Engelen, J.J.M., Marcelis, C.L.M., Alofs, M.G.P., Loneus, W.H., Pulles-Heintzberger, C.F.M., Hamers, A.J.H.

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Duplication of chromosome region (16)(p11.2 → p12.1) in a mother and daughter with mild mental retardation von Engelen, J.J.M., de Die-Smulders, C.E.M., Dirckx, R., Verhoeven, W.M.A., Tuinier, S., Curfs, L.M.G., Hamers, A.J.H.

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Mosaic telomeric (2;14) association in a child with motor delay von Engelen, J.J.M., Marcelis, C., Herbergs, J., Weber, J., Alofs, M., Albrechts, J.C.M., Hamers, A.J.H.

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DOWN SYNDROME AND RELIGIOUS GROUPS von Jongbloet, P.H., Poestkoke, A.J.M., Hamers, A.J.H., Van Erkelens-Zwets, J.H.J.

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Complex Chromosome 9, 20, and 22 Rearrangements in Acute Lymphoblastic Leukemia with Duplication of BCR and ABL Sequences von Stevens-Kroef, M.J.P.L, Dirckx, R, Meers, L.E.C, Albrechts, J.C.M, Schouten, H.C, Hamers, A.J.H

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