First-trimester prenatal diagnosis of a familial subtelomeric translocationKILBY, M. D; BRACKLEY, K. J; WALTERS, J. J et al.Ultrasound in obstetrics & gynecology. 2001, Vol 17, Num 6, pp 531-533, issn 0960-7692Article

Prenatal diagnosis of mosaicism for partial trisomy 8 : A case report including fetal pathologyJAY, A; KILBY, M. D; ROBERTS, E et al.Prenatal diagnosis. 1999, Vol 19, Num 10, pp 976-979, issn 0197-3851Article

High resolution chromosome results in retinoblastoma familiesEMSLIE, J; DAVISON, E. V; ROBERTS, D. F et al.Clinical genetics. 1986, Vol 30, Num 2, pp 117-121, issn 0009-9163Article

Prospective prenatal diagnosis of Prader-Willi syndrome due to maternal disomy for chromosome 15 following trisomic zygote rescueROBERTS, E; STEVENSON, K; COLE, T et al.Prenatal diagnosis. 1997, Vol 17, Num 8, pp 780-783, issn 0197-3851Article

Cytogenetic analysis of a congenital fibrosarcomaADAM, L. R; DAVISON, E. V; MALCOLM, A. J et al.Cancer genetics and cytogenetics. 1991, Vol 52, Num 1, pp 37-41, issn 0165-4608Article

De novo Ph negative T-cell lymphoblastic leukaemia associated with BCR gene rearrangementMIDDLETON, P. G; DAVISON, E. V; REID, M. M et al.Leukemia research. 1990, Vol 14, Num 1, pp 99-103, issn 0145-2126Article

Confined placental mosaicism, IUGR, and adverse pregnancy outcome : a controlled retrospective U.K. collaborative surveyWOLSTENHOLME, J; ROONEY, D. E; DAVISON, E. V et al.Prenatal diagnosis. 1994, Vol 14, Num 5, pp 345-361, issn 0197-3851Article

Partial trisomy 16 as a result of familial 16;20 translocationDAVISON, E. V; BEESLEY, J. R.Journal of medical genetics. 1984, Vol 21, Num 5, pp 384-386, issn 0022-2593Article

Additional information from array comparative genomic hybridization technology over conventional karyotyping in prenatal diagnosis: a systematic review and meta-analysisHILLMAN, S. C; PRETLOVE, S; COOMARASAMY, A et al.Ultrasound in obstetrics & gynecology. 2011, Vol 37, Num 1, pp 6-14, issn 0960-7692, 9 p.Article

A further case of confined placental mosaicism for trisomy 2 associated with adverse pregnancy outcomeROBERTS, Eileen; DUNLOP, J; DAVIS, G. S et al.Prenatal diagnosis. 2003, Vol 23, Num 7, pp 564-565, issn 0197-3851, 2 p.Article

Cytogenetic analysis of a granulocytic sarcoma in a patient without systemic leukaemiaADAM, L. R; ANGUS, B; CAREY, P et al.Journal of clinical pathology. 1991, Vol 44, Num 1, pp 81-82, issn 0021-9746Article

Prader Willi syndrome with hypothyroidismBHATE, M. S; ROBERTSON, P. E; DAVISON, E. V et al.Journal of mental deficiency research. 1989, Vol 33, Num 3, pp 235-244, issn 0022-264XArticle

Rapid prenatal diagnosis of common trisomies : discordant results between QF-PCR analysis and karyotype analysis on long-term culture for a case of trisomy 18 detected in CVSALLEN, S. K; LUHARIA, A; GOULD, C. P et al.Prenatal diagnosis. 2006, Vol 26, Num 12, pp 1160-1167, issn 0197-3851, 8 p.Article

Cytogenetic abnormalities in a disseminated medulloblastomaSTUART, A. G; PEARSON, A. D. J; EMSLIE, J et al.Medical and pediatric oncology. 1993, Vol 21, Num 4, pp 295-298, issn 0098-1532Conference Paper

Meiotic and sperm chromosome analysis in a male carrier of an inverted insertion (3;10)(q13.2;p14p13)GOLDMAN, A. S. H; MARTIN, R. H; JOHANNISSON, R et al.Journal of medical genetics. 1992, Vol 29, Num 7, pp 460-464, issn 0022-2593Article

Translocation t(8;21) associated with marked granulocytic hyperplasiaKOHLI, M; DALY, H; DAVISON, E. V et al.Cancer genetics and cytogenetics. 1988, Vol 31, Num 2, pp 193-197, issn 0165-4608Article

A terminal deletion of the long arm of chromosome 4 [46,XX,del(4)(q33)] in an infant with phenotypic features of Williams syndromeJEFFERSON, R. D; BURN, J; GAUNT, K. L et al.Journal of medical genetics. 1986, Vol 23, Num 5, pp 474-477, issn 0022-2593Article

Epidermal mosaicism and Blaschko's linesMOSS, C; LARKINS, S; STACEY, M et al.Journal of medical genetics. 1993, Vol 30, Num 9, pp 752-755, issn 0022-2593Article

Chromosome 22 abnormalities in Ewing's sarcomaDAVISON, E. V; PEARSON, A. D. J; EMSLIE, J et al.Journal of clinical pathology. 1989, Vol 42, Num 8, pp 797-799, issn 0021-9746Article

Chromosome studies of males in an institution for the mentally handicappedENGLISH, C. J; DAVISON, E. V; BHATE, M. S et al.Journal of medical genetics. 1989, Vol 26, Num 6, pp 379-381, issn 0022-2593, 3 p.Article

Familial myelodysplasia: progressive disease associated with emergence of monosomy 7PAUL, B; REID, M. M; DAVISON, E. V et al.British journal of haematology. 1987, Vol 65, Num 3, pp 321-323, issn 0007-1048Article

Cytogenic investigations in the assessment of response to treatment in neuroblastomaBOWN, N; REID, M. M; PEARSON, A. D. J et al.Journal of clinical pathology. 1987, Vol 40, Num 11, pp 1334-1336, issn 0021-9746Article

Partial trisomy 20p resulting from a recombination of a familial pericentric inversionBOWN, N; CROSS, I; DAVISON, E. V et al.Human genetics. 1986, Vol 74, Num 4, pp 417-419, issn 0340-6717Article

Structural chromosome anomalies in congenital diaphragmatic herniaHOWE, D. T; KILBY, M. D; SIRRY, H et al.Prenatal diagnosis. 1996, Vol 16, Num 11, pp 1003-1009, issn 0197-3851Article

Cytogenetic abnormalities of small round cell tumoursBOWN, N. P; REID, M. M; MALCOLM, A. J et al.Medical and pediatric oncology. 1994, Vol 23, Num 2, pp 124-129, issn 0098-1532Article