FISHWATERS, J. J; BARLOW, A. L; GOULD, C. P et al.MP. Molecular pathology. 1998, Vol 51, Num 2, pp 62-70, issn 1366-8714Article

A DA/DAPI positive human 14p heteromorphism defined by fluorescence in-situ hydridisation using chromosome 15-specific probes D15Z1 (satellite III) and p-TRA-25 (alphoid)STERGIANOU, K; GOULD, C. P; WATERS, J. J et al.Hereditas (Landskrona). 1993, Vol 119, Num 2, pp 105-110, issn 0018-0661Article

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

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

Chromosome in situ suppression hybridisation in clinical cytogeneticsHULTEN, M. A; GOULD, C. P; GOLDMAN, A. S. H et al.Journal of medical genetics. 1991, Vol 28, Num 9, pp 577-582, issn 0022-2593Article