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Two subsets of human alphoid repetitive DNA show distinct preferential localization in the pericentric regions of chromosomes 13, 18, and 21.
Devilee P, Cremer T, Slagboom P, Bakker E, Scholl HP, Hager HD, Stevenson AF, Cornelisse CJ, Pearson PL. Devilee P, et al. Cytogenet Cell Genet. 1986;41(4):193-201. doi: 10.1159/000132229. Cytogenet Cell Genet. 1986. PMID: 3011362
Detection of chromosome aberrations in the human interphase nucleus by visualization of specific target DNAs with radioactive and non-radioactive in situ hybridization techniques: diagnosis of trisomy 18 with probe L1.84.
Cremer T, Landegent J, Brückner A, Scholl HP, Schardin M, Hager HD, Devilee P, Pearson P, van der Ploeg M. Cremer T, et al. Hum Genet. 1986 Dec;74(4):346-52. doi: 10.1007/BF00280484. Hum Genet. 1986. PMID: 3793097
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.
Granzow M, Popp S, Keller M, Holtgreve-Grez H, Brough M, Schoell B, Rauterberg-Ruland I, Hager HD, Tariverdian G, Jauch A. Granzow M, et al. Among authors: hager hd. Hum Genet. 2000 Jul;107(1):51-7. doi: 10.1007/s004390000321. Hum Genet. 2000. PMID: 10982035
High incidence and intraclonal heterogeneity of chromosome 11 aberrations in patients with newly diagnosed multiple myeloma detected by multiprobe interphase FISH.
Cremer FW, Kartal M, Hose D, Bila J, Buck I, Bellos F, Raab MS, Brough M, Moebus A, Hager HD, Goldschmidt H, Moos M, Bartram CR, Jauch A. Cremer FW, et al. Among authors: hager hd. Cancer Genet Cytogenet. 2005 Sep;161(2):116-24. doi: 10.1016/j.cancergencyto.2005.02.015. Cancer Genet Cytogenet. 2005. PMID: 16102581
Novel constitutional t(2;12)(q21;q22) in a patient with t(9;22)-negative chronic myelocytic leukemia.
Krämer A, Fruehauf S, Ho AD, Hager HD, Bartram CR, Hochhaus A. Krämer A, et al. Among authors: hager hd. Cancer Genet Cytogenet. 2003 Apr 15;142(2):162-4. doi: 10.1016/s0165-4608(02)00797-5. Cancer Genet Cytogenet. 2003. PMID: 12699897 No abstract available.
Trisomy 8q and partial trisomy 22 in a 43-year-old man with moderate intellectual disability, epilepsy and large cell non-Hodgkin lymphoma.
Helbig I, Wirtenberger M, Jauch A, Hager HD, Tariverdian G, Hemminki K, Burwinkel B, Klaes R. Helbig I, et al. Among authors: hager hd. Am J Med Genet A. 2006 Aug 1;140(15):1658-62. doi: 10.1002/ajmg.a.31350. Am J Med Genet A. 2006. PMID: 16838305
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