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Results: 1-8 |
Results: 8
Prenatally detected marker chromosome identified as an i(22)(p10) using (micro)FISH
Authors: Engelen, JJM Tuerlings, JHAM Albrechts, JCM Schrander-Stumpel, CTRM Hamers, AJH De Die-Smulders, CEM
Citation: Jjm. Engelen et al., Prenatally detected marker chromosome identified as an i(22)(p10) using (micro)FISH, GEN COUNSEL, 11(1), 2000, pp. 13-17
Complex chromosome 9, 20, and 22 rearrangements in acute lymphoblastic leukemia with duplication of BCR and ABL sequences
Authors: Stevens-Kroef, MJPL Dirckx, R Meers, LEC Albrechts, JCM Schouten, HC Hamers, AJH
Citation: Mjpl. Stevens-kroef et al., Complex chromosome 9, 20, and 22 rearrangements in acute lymphoblastic leukemia with duplication of BCR and ABL sequences, CANC GENET, 116(2), 2000, pp. 119-123
Familial dup(8)(p12p21.1): Mild phenotypic effect and review of partial 8pduplications
Authors: Moog, U Engelen, JJM Albrechts, JCM Baars, LGM de Die-Smulders, CEM
Citation: U. Moog et al., Familial dup(8)(p12p21.1): Mild phenotypic effect and review of partial 8pduplications, AM J MED G, 94(4), 2000, pp. 306-310
Mosaic telomeric (2;14) association in a child with motor delay
Authors: Engelen, JJM Marcelis, C Herbergs, J Weber, J Alofs, M Albrechts, JCM Hamers, AJH
Citation: Jjm. Engelen et al., Mosaic telomeric (2;14) association in a child with motor delay, AM J MED G, 92(5), 2000, pp. 318-321
Duplication of chromosome region 8p23.1 -> p23.3: A benign variant?
Authors: Engelen, JJM Moog, U Evers, JLH Dassen, H Albrechts, JCM Hamers, AJH
Citation: Jjm. Engelen et al., Duplication of chromosome region 8p23.1 -> p23.3: A benign variant?, AM J MED G, 91(1), 2000, pp. 18-21
Assignment of the human gene for endosarcomeric cytoskeletal M-protein (MYOM2) to 8p23.3
Authors: van der Ven, PFM Speel, EJM Albrechts, JCM Ramaekers, FCS Hopman, AHN Furst, DO
Citation: Pfm. Van Der Ven et al., Assignment of the human gene for endosarcomeric cytoskeletal M-protein (MYOM2) to 8p23.3, GENOMICS, 55(2), 1999, pp. 253-255
Detection of a cryptic translocation t(13;20)(q34;p13) in an unexplained case of MCA/MR: Value of FISH over high resolution banding
Authors: de Die-Smulders, CEM Engelen, JJM Albrechts, JCM Hamers, GJH
Citation: Cem. De Die-smulders et al., Detection of a cryptic translocation t(13;20)(q34;p13) in an unexplained case of MCA/MR: Value of FISH over high resolution banding, AM J MED G, 86(4), 1999, pp. 385-388
Characterization of a partial trisomy 16q with fish - Report of a patient and review of the literature
Authors: Engelen, JJM De Die-Smulders, CEM Vos, PTH Meers, LEC Albrechts, JCM Hamers, AJH
Citation: Jjm. Engelen et al., Characterization of a partial trisomy 16q with fish - Report of a patient and review of the literature, ANN GENET, 42(2), 1999, pp. 101-104
Risultati: 1-8 |