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Results: 1-9 |
Results: 9
Characterization of the TBX5 binding site and analysis of mutations that cause Holt-Oram syndrome
Authors: Ghosh, TK Packham, EA Bonser, AJ Robinson, TE Cross, SJ Brook, JD
Citation: Tk. Ghosh et al., Characterization of the TBX5 binding site and analysis of mutations that cause Holt-Oram syndrome, HUM MOL GEN, 10(18), 2001, pp. 1983-1994
In vivo co-localisation of MBNL protein with DMPK expanded-repeat transcripts
Authors: Fardaei, M Larkin, K Brook, JD Hamshere, MG
Citation: M. Fardaei et al., In vivo co-localisation of MBNL protein with DMPK expanded-repeat transcripts, NUCL ACID R, 29(13), 2001, pp. 2766-2771
Virtual cloning and physical mapping of a human T-box gene, TBX4
Authors: Yi, CH Russ, A Brook, JD
Citation: Ch. Yi et al., Virtual cloning and physical mapping of a human T-box gene, TBX4, GENOMICS, 67(1), 2000, pp. 92-95
A transcript map of a 10-Mb region of chromosome 19: A source of genes forhuman disorders, including candidates for genes involved in asthma, heart defects, and eye development
Authors: Hamshere, M Cross, S Daniels, M Lennon, G Brook, JD
Citation: M. Hamshere et al., A transcript map of a 10-Mb region of chromosome 19: A source of genes forhuman disorders, including candidates for genes involved in asthma, heart defects, and eye development, GENOMICS, 63(3), 2000, pp. 425-429
Loss of heterozygosity in bilateral breast cancer
Authors: Kollias, J Man, S Marafie, M Carpenter, K Pinder, S Ellis, IO Blamey, RW Cross, G Brook, JD
Citation: J. Kollias et al., Loss of heterozygosity in bilateral breast cancer, BREAST CANC, 64(3), 2000, pp. 241-251
The mutation spectrum in Holt-Oram syndrome
Authors: Cross, SJ Ching, YH Li, QY Armstrong-Buisseret, L Spranger, S Lyonnet, S Bonnet, D Penttinen, M Jonveaux, P Leheup, B Mortier, G Van Ravenswaaij, C Gardiner, CA Brook, JD Newbury-Ecob, R
Citation: Sj. Cross et al., The mutation spectrum in Holt-Oram syndrome, J MED GENET, 37(10), 2000, pp. 785-787
Myotonic dystrophy is associated with a reduced level of RNA from the DMWDallele adjacent to the expanded repeat
Authors: Alwazzan, M Newman, E Hamshere, MG Brook, JD
Citation: M. Alwazzan et al., Myotonic dystrophy is associated with a reduced level of RNA from the DMWDallele adjacent to the expanded repeat, HUM MOL GEN, 8(8), 1999, pp. 1491-1497
Identification, mapping, and phylogenomic analysis of four new human members of the T-box gene family: EOMES, TBX6, TBX18, and TBX19
Authors: Yi, CH Terrett, JA Li, QY Ellington, K Packham, EA Armstrong-Buisseret, L McClure, P Slingsby, T Brook, JD
Citation: Ch. Yi et al., Identification, mapping, and phylogenomic analysis of four new human members of the T-box gene family: EOMES, TBX6, TBX18, and TBX19, GENOMICS, 55(1), 1999, pp. 10-20
Myotonic dystrophy: the correlation of (CTG) repeat length in leucocytes with age at onset is significant only for patients with small expansions
Authors: Hamshere, MG Harley, H Harper, P Brook, JD Brookfield, JFY
Citation: Mg. Hamshere et al., Myotonic dystrophy: the correlation of (CTG) repeat length in leucocytes with age at onset is significant only for patients with small expansions, J MED GENET, 36(1), 1999, pp. 59-61
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