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Page 1
Second report on chicken genes and chromosomes 2005.
Schmid M, Nanda I, Hoehn H, Schartl M, Haaf T, Buerstedde JM, Arakawa H, Caldwell RB, Weigend S, Burt DW, Smith J, Griffin DK, Masabanda JS, Groenen MA, Crooijmans RP, Vignal A, Fillon V, Morisson M, Pitel F, Vignoles M, Garrigues A, Gellin J, Rodionov AV, Galkina SA, Lukina NA, Ben-Ari G, Blum S, Hillel J, Twito T, Lavi U, David L, Feldman MW, Delany ME, Conley CA, Fowler VM, Hedges SB, Godbout R, Katyal S, Smith C, Hudson Q, Sinclair A, Mizuno S. Schmid M, et al. Among authors: hoehn h. Cytogenet Genome Res. 2005;109(4):415-79. doi: 10.1159/000084205. Cytogenet Genome Res. 2005. PMID: 15905640 Free article. Review. No abstract available.
Disruption of the FA/BRCA pathway in bladder cancer.
Neveling K, Kalb R, Florl AR, Herterich S, Friedl R, Hoehn H, Hader C, Hartmann FH, Nanda I, Steinlein C, Schmid M, Tonnies H, Hurst CD, Knowles MA, Hanenberg H, Schulz WA, Schindler D. Neveling K, et al. Among authors: hoehn h. Cytogenet Genome Res. 2007;118(2-4):166-76. doi: 10.1159/000108297. Cytogenet Genome Res. 2007. PMID: 18000367
Spectral karyotyping of Werner syndrome fibroblast cultures.
Melcher R, von Golitschek R, Steinlein C, Schindler D, Neitzel H, Kainer K, Schmid M, Hoehn H. Melcher R, et al. Among authors: hoehn h. Cytogenet Cell Genet. 2000;91(1-4):180-5. doi: 10.1159/000056841. Cytogenet Cell Genet. 2000. PMID: 11173853
Genetic instability syndromes with progeroid features.
Neveling K, Bechtold A, Hoehn H. Neveling K, et al. Among authors: hoehn h. Z Gerontol Geriatr. 2007 Oct;40(5):339-48. doi: 10.1007/s00391-007-0483-x. Z Gerontol Geriatr. 2007. PMID: 17943237 Review.
The Fanconi anaemia group G gene FANCG is identical with XRCC9.
de Winter JP, Waisfisz Q, Rooimans MA, van Berkel CG, Bosnoyan-Collins L, Alon N, Carreau M, Bender O, Demuth I, Schindler D, Pronk JC, Arwert F, Hoehn H, Digweed M, Buchwald M, Joenje H. de Winter JP, et al. Among authors: hoehn h. Nat Genet. 1998 Nov;20(3):281-3. doi: 10.1038/3093. Nat Genet. 1998. PMID: 9806548
Localisation of a Fanconi anaemia gene to chromosome 9p.
Saar K, Schindler D, Wegner RD, Reis A, Wienker TF, Hoehn H, Joenje H, Sperling K, Digweed M. Saar K, et al. Among authors: hoehn h. Eur J Hum Genet. 1998 Sep-Oct;6(5):501-8. doi: 10.1038/sj.ejhg.5200241. Eur J Hum Genet. 1998. PMID: 9801875
156 results