Cutaneous clues for diagnosing X-chromosomal disorders von Vreeburg, M., Sallevelt, S.C.E.H., Stegmann, A.P.A., van Geel, M., Detisch, Y.J.H.A., Schrander-Stumpel, C.T.R.M., van Steensel, M.A.M., Marcus-Soekarman, D.

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Skin changes in oculo‐dento‐digital dysplasia are correlated with C‐terminal truncations of connexin 43 von Vreeburg, M., de Zwart‐Storm, E.A., Schouten, M.I., Nellen, R.G.L., Marcus‐Soekarman, D., Devies, M., van Geel, M., van Steensel, M.A.M.

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Novel EBP gene mutations in Conradi-Hünermann-Happle syndrome von Steijlen, P.M., Van Geel, M., Vreeburg, M., Marcus-Soekarman, D., Spaapen, L.J.M., Castelijns, F.C.M., Willemsen, M., Van Steensel, M.A.M.

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Prenatal diagnosis of bronchial atresia, early in pregnancy von Duin, L. K., Marcus-Soekarman, D., Baldewijns, M. M. L., Robben, S. G. F., Nijhuis, J. G.

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Mosaic trisomy 11p in monozygotic twins with discordant clinical phenotypes von Marcus-Soekarman, D., Hamers, G., Velzeboer, S., Nijhuis, J., Loneus, W.H., Herbergs, J., de Die-Smulders, C., Schrander-Stumpel, C., Engelen, J.

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Spinal anesthesia for a parturient with the triad of Currarino von van der Heijden, M.W.J, Smits, H, Willekes, C, Marcus-Soekarman, D, Wilmink, J.T, Marcus, M.A.E

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Sonographic genital ambiguity in a fetus due to a mosaic 45,X/46,X,idic(Y)(qter-p11.32::p11.32-qter) karyotype von Marcus-Soekarman, D., Hamers, G., Mulder, A. L. M., Offermans, Jeanne, Offermans, Jos, Engelen, J., van Lent-Albrechts, J. C. M., Robben, S. G. F., de Muinck Keizer-Schrama, S., Wolffenbuttel, K. P., Looijenga, L. H. J., Oosterhuis, J. W., Schrander-Stumpel, C., Nijhuis, J.

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Epidural Local Anesthetics: A Novel Treatment for Fetal Growth Retardation? von Strümper, D., Louwen, F., Durieux, M.E., Gramke, H.F., Stuessel, J., Marcus-Soekarman, D., van Aken, H., Marcus, M.A.E.

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Hyperechogenic fetal bowel: counseling difficulties von Marcus-Soekarman, D., Offermans, J., Van den Ouweland, A.M.W., Mulder, A.L.M., Muntjewerff, N., Vossen, M., Kleijer, W., Schrander-Stumpel, C., Dooijes, D.

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The Translocation (6;9) (p23;q34) Shows Consistent Rearrangement of Two Genes and Defines a Myeloproliferative Disorder With Specific Clinical Features von Soekarman, D., Lindern, M. von, Daenen, S., Jong, B. de, Fonatsch, C., Heinze, B., Bartram, C., Hagemeijer, A., Grosveld, G.

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Cytogenetic and molecular analysis in Philadelphia negative CML von van der Plas, DC, Hermans, AB, Soekarman, D, Smit, EM, de Klein, A, Smadja, N, Alimena, G, Goudsmit, R, Grosveld, G, Hagemeijer, A

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Cytogenetic and Molecular Analysis in Philadelphia Negative CML von der Plas, D.C. van, Hermans, A.B.C., Soekarman, D., Smit, E.M.E., Klein, A. de, Smadja, N., Alimena, G., Goudsmit, R., Grosveld, G., Hagemeijer, A.

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Sonographic genital ambiguity in a fetus due to a mosaic 45,X/46,X,idic(Y)(qter-p11.32::p11.32-qter) karyotype: ISODICENTRIC Y-CHROMOSOME von Marcus-Soekarman, D., Hamers, G., Mulder, A. L. M., Offermans, Jeanne, Offermans, Jos, Engelen, J., van Lent-Albrechts, J. C. M., Robben, S. G. F., de Muinck Keizer-Schrama, S., Wolffenbuttel, K. P., Looijenga, L. H. J., Oosterhuis, J. W., Schrander-Stumpel, C., Nijhuis, J.

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Hypohidrotic ectodermal dysplasia, central nervous system malformation, and distinct facial features: confirmation of a distinct entity? von Soekarman, D, Fryns, J P

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The translocation (6;9) (p23;q34) shows consistent rearrangement of two genes and defines a myeloproliferative disorder with specific clinical features von Soekarman, D, von Lindern, M, Daenen, S, de Jong, B, Fonatsch, C, Heinze, B, Bartram, C, Hagemeijer, A, Grosveld, G

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The translocation (6;9) (p23;q34) shows consistent rearrangement of two genes and defines a mueloproliferative disorder with specitif clinical features von SOEKARMAN, D, VON LINDERN, M, DAENEN, S, DE JONG, B, FONATSCH, C, HEINZE, B, BARTRAM, C, HAGERMEIJER, A, GROSVELD, G

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Prenatal diagnosis of bronchial atresia, early in pregnancy von Duin, L K, Marcus-Soekarman, D, Baldewijns, M M L, Robben, S G F, Nijhuis, J G

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Skin changes in oculo-dento-digital dysplasia are correlated with C-terminal truncations of connexin 43 von Vreeburg, M., de Zwart-Storm, E.A., Schouten, M.I., Nellen, R.G.L., Marcus-Soekarman, D., Devies, M., van Geel, M., van Steensel, M.A.M.

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Type IX collagen gene mutations can result in multiple epiphyseal dysplasia that is associated with osteochondritis dissecans and a mild myopathy von Jackson, Gail C., Marcus-Soekarman, Dominique, Stolte-Dijkstra, Irene, Verrips, Aad, Taylor, Jacqueline A., Briggs, Michael D.

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Translocation t(6;9) in acute non-lymphocytic leukaemia results in the formation of a DEK-CAN fusion gene von Von Lindern, Marieke, Fornerod, Maarten, Soekarman, Nike, Van Baal, Sjozèf, Jaegle, Martine, Hagemeijer, Anne, Bootsma, Dirk, Grosveld, Gerard

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