Results: 1-18 |
Results: 18

Authors: Hanson, H Mathew, CG Docherty, Z Ogilvie, CM
Citation: H. Hanson et al., Telomere shortening in Fanconi anaemia demonstrated by a direct FISH approach, CYTOG C GEN, 93(3-4), 2001, pp. 203-206

Authors: Ogilvie, CM Harrison, RH Horsley, SW Hodgson, SV Kearney, L
Citation: Cm. Ogilvie et al., A mitotically stable marker chromosome negative for whole chromosome libraries, centromere probes and chromosome specific telomere regions: a novel class of supernumerary marker chromosome?, CYTOG C GEN, 92(1-2), 2001, pp. 69-73

Authors: Pettigrew, R Kuo, HC Scriven, P Rowell, P Pal, K Handyside, A Braude, P Ogilvie, CM
Citation: R. Pettigrew et al., A pregnancy following PGD for X-linked autosomal dominant Incontinentia Pigmenti (Bloch-Sulzberger syndrome): Case report (vol 15, pg 2650, 2000), HUM REPR, 16(6), 2001, pp. 1308-1308

Authors: Scriven, PN Flinter, FA Braude, PR Ogilvie, CM
Citation: Pn. Scriven et al., Robertsonian translocations - reproductive risks and indications for preimplantation genetic diagnosis, HUM REPR, 16(11), 2001, pp. 2267-2273

Authors: Mann, K Ogilvie, CM
Citation: K. Mann et Cm. Ogilvie, Prenatal detection of chromosome disorders, LANCET, 358(9293), 2001, pp. 1646-1646

Authors: Mann, K Fox, SP Abbs, SJ Yau, SC Scriven, PN Docherty, Z Ogilvie, CM
Citation: K. Mann et al., Development and implementation of a new rapid aneuploidy diagnostic service within the UK National Health Service and implications for the future of prenatal diagnosis, LANCET, 358(9287), 2001, pp. 1057-1061

Authors: Boorman, JG Varma, S Ogilvie, CM
Citation: Jg. Boorman et al., Velopharyngeal incompetence and chromosome 22q11 deletion, LANCET, 357(9258), 2001, pp. 774-774

Authors: Ogilvie, CM Phil, D Scriven, PN
Citation: Cm. Ogilvie et al., The scope and limitations of "FISH" for preimplantation genetic diagnosis, FERT STERIL, 75(1), 2001, pp. 227-228

Authors: Ogilvie, CM Kasten, P Rovinsky, D Workman, KL Johnston, JO
Citation: Cm. Ogilvie et al., Cysticercosis of the triceps - An unusual pseudotumor - Case report and review, CLIN ORTHOP, (382), 2001, pp. 217-221

Authors: Pettigrew, R Kuo, HC Scriven, P Rowell, P Pal, K Handyside, A Braude, P Ogilvie, CM
Citation: R. Pettigrew et al., A pregnancy following PGD for X-linked autosomal dominant Incontinentia Pigmenti (Bloch-Sulzberger syndrome), HUM REPR, 15(12), 2000, pp. 2650-2652

Authors: Scriven, PN O'Mahony, F Bickerstaff, H Yeong, CT Braude, P Ogilvie, CM
Citation: Pn. Scriven et al., Clinical pregnancy following blastomere biopsy and PGD for a reciprocal translocation carrier: analysis of meiotic outcomes and embryo quality in twoIVF cycles, PRENAT DIAG, 20(7), 2000, pp. 587-592

Authors: Ogilvie, CM Shemilt, S Davies, AF Weber-Hall, S Chuang, CY Sundaresan, V
Citation: Cm. Ogilvie et al., Characterization of a chromosomally complex lung cancer cell line using multiwell fluorescence in situ hybridization, CANC GENET, 117(2), 2000, pp. 149-152

Authors: Ogilvie, CM Moore, J Daker, M Palferman, S Docherty, Z
Citation: Cm. Ogilvie et al., Chromosome 22q11 deletions are not found in autistic patients identified using strict diagnostic criteria, AM J MED G, 96(1), 2000, pp. 15-17

Authors: Warburton, P Mohammed, S Ogilvie, CM
Citation: P. Warburton et al., Detection of submicroscopic subtelomeric chromosome translocations: A new case study, AM J MED G, 91(1), 2000, pp. 51-55

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

Authors: Abusaad, I Mohammed, SN Ogilvie, CM Ritchie, J Pohl, KRE Docherty, Z
Citation: I. Abusaad et al., Clinical expression of menkes disease in a girl with X;13 translocation, AM J MED G, 87(4), 1999, pp. 354-359

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

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: 1-18 |