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Results: 1-25 | 26-29
Results: 1-25/29

Authors: Thai, TP Rodemer, C Jauch, A Hunziker, A Moser, A Gorgas, K Just, WW
Citation: Tp. Thai et al., Impaired membrane traffic in defective ether lipid biosynthesis, HUM MOL GEN, 10(2), 2001, pp. 127-136

Authors: Scheel, C Schaefer, KL Jauch, A Keller, M Wai, D Brinkschmidt, C van Valen, F Boecker, W Dockhorn-Dworniczak, B Poremba, C
Citation: C. Scheel et al., Alternative lengthening of telomeres is associated with chromosomal instability in osteosarcomas, ONCOGENE, 20(29), 2001, pp. 3835-3844

Authors: Granzow, M Popp, S Weber, S Schoell, B Holtgreve-Grez, H Senf, L Hager, D Boschert, J Scheurlen, W Jauch, A
Citation: M. Granzow et al., Isochromosome 1q as an early genetic event in a child with intracranial ependymoma characterized by molecular cytogenetics, CANC GENET, 130(1), 2001, pp. 79-83

Authors: Sharma, P Jarvis, A Jauch, A St Heaps, L Shaw, P Smith, A
Citation: P. Sharma et al., Complex variant t(4;11) characterized by fluorescence in situ hybridization in infant acute lymphoblastic leukemia, CANC GENET, 127(2), 2001, pp. 177-180

Authors: Scholz, I Popp, S Granzow, M Schoell, B Holtgreve-Grez, H Takeuchi, S Schrappe, M Harbott, J Teigler-Schlegel, A Zimmermann, M Fischer, C Koeffler, HP Bartram, CR Jauch, A
Citation: I. Scholz et al., Comparative genomic hybridization in childhood acute lymphoblastic leukemia: correlation with interphase cytogenetics and loss of heterozygosity analysis, CANC GENET, 124(2), 2001, pp. 89-97

Authors: Reinehr, T Jauch, A Zoll, B Engel, U Bartels, I Andler, W
Citation: T. Reinehr et al., Short stature in a mother and daughter caused by familial der(X)t(X;X)(p22.1-3;q26), AM J MED G, 102(1), 2001, pp. 81-85

Authors: Trautmann, K Thakker, RV Ellison, DW Ibrahim, A Lees, PD Harding, B Fischer, C Popp, S Bartram, CR Jauch, A
Citation: K. Trautmann et al., Chromosomal aberrations in sporadic pituitary tumors, INT J CANC, 91(6), 2001, pp. 809-814

Authors: Tsukasaki, K Krebs, J Nagai, K Tomonaga, M Koeffler, HP Bartram, CR Jauch, A
Citation: K. Tsukasaki et al., Comparative genomic hybridization analysis in adult T-cell leukemia/lymphoma: correlation with clinical course, BLOOD, 97(12), 2001, pp. 3875-3881

Authors: Herbort, CP Jauch, A Othenin-Girard, P Tritten, JJ Fsadni, M
Citation: Cp. Herbort et al., Diclofenac drops to treat inflammation after cataract surgery, ACT OPHTH S, 78(4), 2000, pp. 421-424

Authors: Brown, J Horsley, SW Jung, C Saracoglu, K Janssen, B Brough, M Daschner, M Beedgen, B Kerkhoffs, G Eils, R Harris, PC Jauch, A Kearney, L
Citation: J. Brown et al., Identification of a subtle t(16;19)(p13.3;p13.3) in an infant with multiple congenital abnormalities using a 12-colour multiplex FISH telomere assay,M-TEL, EUR J HUM G, 8(12), 2000, pp. 903-910

Authors: Sperandio, M Weber, L Jauch, A Janssen, B Mehls, O Schaefer, F
Citation: M. Sperandio et al., Cutaneous white spots in a child with polycystic kidneys: a clue to TSC2/PKD1 gene mutation, NEPH DIAL T, 15(6), 2000, pp. 909-912

Authors: Granzow, M Popp, S Keller, M Holtgreve-Grez, H Brough, M Schoell, B Rauterberg-Ruland, I Hager, HD Tariverdian, G Jauch, A
Citation: M. Granzow et al., Multiplex FISH telomere integrity assay identifies an unbalanced cryptic translocation der(5)t(3;5) (q27;p15.3) in a family with three mentally retarded individuals, HUM GENET, 107(1), 2000, pp. 51-57

Authors: Speleman, F Callens, B Logghe, K Van Roy, N Horsley, SW Jauch, A Verschraegen-Spae, MR Leroy, JG
Citation: F. Speleman et al., Subtelomeric familial translocation t(2;7)(q37;q35) leading to partial trisomy 7q35 -> qter: Molecular cytogenetic analysis and clinical phenotype intwo generations, AM J MED G, 93(5), 2000, pp. 349-354

Authors: Spranger, S Rommel, B Jauch, A Bodammer, R Mehl, B Bullerdiek, J
Citation: S. Spranger et al., Interstitial deletion of 5q33.3q35.1 in a girl with mild mental retardation, AM J MED G, 93(2), 2000, pp. 107-109

Authors: Oner, G Jauch, A Eggermann, T Hardwick, R Kirsch, S Schiebel, K Rappold, G Robson, L Smith, A
Citation: G. Oner et al., Mosaic rearrangement of chromosome 18: Characterization by FISH mapping and DNA studies shows trisomy 18p and monosomy 18p both of paternal origin, AM J MED G, 92(2), 2000, pp. 101-106

Authors: Bergmann, C Senderek, J Hermanns, B Jauch, A Janssen, D Schroder, JM Karch, D
Citation: C. Bergmann et al., Becker muscular dystrophy combined with X-linked Charcot-Marie-Tooth neuropathy, MUSCLE NERV, 23(5), 2000, pp. 818-823

Authors: von Knobloch, R Bugert, P Jauch, A Kalble, T Kovacs, G
Citation: R. Von Knobloch et al., Allelic changes at multiple regions of chromosome 5 are associated with progression of urinary bladder cancer, J PATHOLOGY, 190(2), 2000, pp. 163-168

Authors: Popp, S Waltering, S Holtgreve-Grez, H Jauch, A Proby, C Leigh, IM Boukamp, P
Citation: S. Popp et al., Genetic characterization of a human skin carcinoma progression model: fromprimary tumor to metastasis, J INVES DER, 115(6), 2000, pp. 1095-1103

Authors: Klugbauer, S Jauch, A Lengfelder, E Demidchik, E Rabes, HM
Citation: S. Klugbauer et al., A novel type of RET rearrangement (PTC8) in childhood papillary thyroid carcinomas and characterization of the involved gene (RFG8), CANCER RES, 60(24), 2000, pp. 7028-7032

Authors: Janssen, JWG Vaandrager, JW Heuser, T Jauch, A Kluin, PM Geelen, E Bergsagel, PL Kuehl, WM Drexler, HG Otsuki, T Bartram, CR Schuuring, E
Citation: Jwg. Janssen et al., Concurrent activation of a novel putative transforming gene, myeov, and cyclin D1 in a subset of multiple myeloma cell lines with t(11;14)(q13;q32), BLOOD, 95(8), 2000, pp. 2691-2698

Authors: Smith, A Jauch, A St Heaps, L Robson, L Kearney, B
Citation: A. Smith et al., Unbalanced translocation t(15;22) in 'severe' Prader-Willi syndrome, ANN GENET, 43(3-4), 2000, pp. 125-130

Authors: Williamson, C Cavaco, BM Jauch, A Dixon, PH Forbes, S Harding, B Holtgreve-Grez, H Schoell, B Pereira, MC Font, AP Loureiro, MM Sobrinho, LG Santos, MA Thakker, RV
Citation: C. Williamson et al., Mapping the gene causing hereditary primary hyperparathyroidism in a Portuguese kindred to chromosome 1q22-q31 (vol 14, pg 230, 1999), J BONE MIN, 14(8), 1999, pp. 1472-1472

Authors: Jauch, A Fsadni, M Gamba, G
Citation: A. Jauch et al., Meta-analysis of six clinical phase III studies comparing lomefloxacin 0.3% eye drops twice daily to five standard antibiotics in patients with acutebacterial conjunctivitis, GR ARCH CL, 237(9), 1999, pp. 705-713

Authors: Smith, A Jauch, A Slater, H Robson, L Sandanam, T
Citation: A. Smith et al., Syndromal obesity due to paternal duplication 6(q24.3-q27), AM J MED G, 84(2), 1999, pp. 125-131

Authors: Mowat, D Jauch, A Robson, L Smith, A
Citation: D. Mowat et al., Duplication within chromosome 5q characterized by fluorescence in situ hybridization, AM J MED G, 83(5), 1999, pp. 361-364
Risultati: 1-25 | 26-29