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Results: 1-11 |
Results: 11
Quantitative measurement of transcript levels throughout human preimplantation development: analysis of hypoxanthine phosphoribosyl transferase
Authors: Taylor, DM Handyside, AH Ray, PF Dibb, NJ Winston, RML Ao, A
Citation: Dm. Taylor et al., Quantitative measurement of transcript levels throughout human preimplantation development: analysis of hypoxanthine phosphoribosyl transferase, MOL HUM REP, 7(2), 2001, pp. 147-154
Controlling misdiagnosis errors in preimplantation genetic diagnosis: a comprehensive model encompassing extrinsic and intrinsic sources of error
Authors: Lewis, CM Pinel, T Whittaker, JC Handyside, AH
Citation: Cm. Lewis et al., Controlling misdiagnosis errors in preimplantation genetic diagnosis: a comprehensive model encompassing extrinsic and intrinsic sources of error, HUM REPR, 16(1), 2001, pp. 43-50
A comparison of different lysis buffers to assess allele dropout from single cells for preimplantation genetic diagnosis
Authors: Thornhill, AR McGrath, JA Eady, RAJ Braude, PR Handyside, AH
Citation: Ar. Thornhill et al., A comparison of different lysis buffers to assess allele dropout from single cells for preimplantation genetic diagnosis, PRENAT DIAG, 21(6), 2001, pp. 490-497
Preimplantation genetic diagnosis of compound heterozygous mutations leading to ablation of plakophilin-1 (PKP1) and resulting in skin fragility ectodermal dysplasia syndrome: a case report
Authors: Thornhill, AR Pickering, SJ Whittock, NV Caller, J Andritsos, V Bickerstaff, HE Handyside, AH Eady, RAJ Braude, PR McGrath, JA
Citation: Ar. Thornhill et al., Preimplantation genetic diagnosis of compound heterozygous mutations leading to ablation of plakophilin-1 (PKP1) and resulting in skin fragility ectodermal dysplasia syndrome: a case report, PRENAT DIAG, 20(13), 2000, pp. 1055-1062
Screening oocytes and preimplantation embryos for aneuploidy
Authors: Handyside, AH Ogilvie, CM
Citation: Ah. Handyside et Cm. Ogilvie, Screening oocytes and preimplantation embryos for aneuploidy, CUR OP OBST, 11(3), 1999, pp. 301-305
Detailed chromosomal and molecular genetic analysis of single cells by whole genome amplification and comparative genomic hybridisation
Authors: Wells, D Sherlock, JK Handyside, AH Delhanty, JDA
Citation: D. Wells et al., Detailed chromosomal and molecular genetic analysis of single cells by whole genome amplification and comparative genomic hybridisation, NUCL ACID R, 27(4), 1999, pp. 1214-1218
Successful preimplantation genetic diagnosis for sex linked Lesch-Nyhan syndrome using specific diagnosis
Authors: Ray, PF Harper, JC Ao, A Taylor, DM Winston, RML Hughes, M Handyside, AH
Citation: Pf. Ray et al., Successful preimplantation genetic diagnosis for sex linked Lesch-Nyhan syndrome using specific diagnosis, PRENAT DIAG, 19(13), 1999, pp. 1237-1241
The future of preimplantation genetic diagnosis
Authors: Handyside, AH Scriven, PN Ogilvie, CM
Citation: Ah. Handyside et al., The future of preimplantation genetic diagnosis, HUM REPR, 13, 1998, pp. 249-255
Clinical evaluation of preimplantation genetic diagnosis
Authors: Handyside, AH
Citation: Ah. Handyside, Clinical evaluation of preimplantation genetic diagnosis, PRENAT DIAG, 18(13), 1998, pp. 1345-1348
Assessment of the reliability of single blastomere analysis for preimplantation diagnosis of the Delta F508 deletion causing cystic fibrosis in clinical practice
Authors: Ray, PF Ao, A Taylor, DM Winston, RML Handyside, AH
Citation: Pf. Ray et al., Assessment of the reliability of single blastomere analysis for preimplantation diagnosis of the Delta F508 deletion causing cystic fibrosis in clinical practice, PRENAT DIAG, 18(13), 1998, pp. 1402-1412
Chromosome translocations: Segregation modes and strategies for preimplantation genetic diagnosis
Authors: Scriven, PN Handyside, AH Ogilvie, CM
Citation: Pn. Scriven et al., Chromosome translocations: Segregation modes and strategies for preimplantation genetic diagnosis, PRENAT DIAG, 18(13), 1998, pp. 1437-1449
Risultati: 1-11 |