The most common fragile site in man is 3p14 von SMEETS, D. F. C. M, SCHERES, J. M. J. C, HUSTINX, T. W. J

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Absence of Y-specific DNA sequences in human 46,XX true hermaphrodites and in 45,X mixed gonadal dysgenesis von WAIBEL, F, SCHERER, G, FRACCARO, M, HUSTINX, T. W. J, WEISSENBACH, J, WIELAND, J, MAYEROVA, A, BACK, E, WOLF, U

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Paracentric inversion inv(11) (q21q23) in the Netherlands von MADAN, K, PIETERS, M. H. E. C, SMEETS, D. F. C. M, KUYT, L. P, VAN ASPEREN, C. J, DE PATER, J. M, HAMERS, A. J. H, GERSSEN-SCHOORL, K. B. J, HUSTINX, T. W. J, BREED, A. S. P. M, VAN HEMEL, J. O

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The fragile site on chromosome 3 von SMEETS, D. F. C. M, SCHERES, J. M. J. C, HUSTINX, T. W. J

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Demonstration of X chromatin in drumstick-like nuclear appendages of leukocytes by in situ hybridization on blood smears von Hochstenbach, P. F. R., Scheres, J. M. J. C., Hustinx, T. W. J., Wieringa, B.

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Localization of Haptoglobin and ABO von HUSTINX, T. W. J, BIJLSMA, J. B, NIJENHUIS, L. E

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Malignant histiocytosis. Clinical and cytogenetic studies in a newborn and a child von Schouten, Teunis J., Hustinx, Theo W. J., Scheres, Jacques M. J. C., Holland, Roland, de Vaan, Gérard A. M.

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The 11q;22q translocation: a European collaborative analysis of 43 cases von Fraccaro, M, Lindsten, J, Ford, C E, Iselius, L

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Prometaphase banding of human chromosomes with basic fuchsin von Scheres, J M, Merkx, G F, Hustinx, T W

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Karyotype instability with multiple 7/14 and 7/7 rearrangements von Hustinx, T W, Scheres, J M, Weemaes, C M, ter Haar, B G, Janssen, A H

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Connatal Pelizaeus-Merzbacher disease with congenital stridor in two maternal cousins von Renier, W O, Gabreëls, F J, Hustinx, T W, Jaspar, H H, Geelen, J A, Van Haelst, U J, Lommen, E J, Ter Haar, B G

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A case of AMMoL with 8/21 translocation and loss of the Y as probably secondary events von Hustinx, T. W. J., Burghouts, J. T. M., Scheres, J. M. J. C., Smits, A. P. T.

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Further delineation of the Nijmegen breakage syndrome von Taalman, Rob D. F. M., Hustinx, Theo W. J., Weemaes, Corry M. R., Seemanová, Eva, Schmidt, Angela, Passarge, Eberhard, Scheres, Jacques M. J. C.

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157 MICROCEPHALY WITH IMMUNODEFICIENCY AND CHROMOSOME INSTABILITY von Weemaes, C M R, Hustinx, T W J, Taalman, R D F M, Scheres, J M J C, Seemanova, E, Passarge, E

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15/17 translocation in acute promyelocytic leukaemia von Scheres, J M, Hustinx, T W, de Vaan, G A, Rutten, F J

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A case of chronic myeloid leukemia with a translocation (12;22)(p13;q11) von van der Blij-Philipsen, M, Breed, W P, Hustinx, T W

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Translocation 1;7 in hematologic disorders: A brief review of 22 cases von Scheres, Jacques M.J.C., Hustinx, Theo W.J., Geraedts, Joep P.M., Leeksma, C.Henk W., Meltzer, Paul S.

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Possible involvement of unstable sites on chromosomes 7 and 14 in human cancer von Scheres, Jacques M.J.C., Hustinx, T.W.J., Trent, Jeffrey M.

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A RING-X-CHROMOSOME IN PART OF THE SOMATIC CELLS OF A PATIENT WITH SOME CHARACTERISTICS OF THE TURNER SYNDROME von HUSTINX, T W, STOELINGA, G B

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An XYY chromosome pattern in a boy with Marfan's syndrome von Hustinx, T. W. J., van Olphen, A. H. F.

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