Fragile site Xq27.3 in a family without mental retardationROMAIN, D. R; CHAPMAN, C. J.Clinical genetics. 1992, Vol 41, Num 1, pp 33-35, issn 0009-9163Article

Trisomy 18 with karyotype 47,XX,-18+i psu dic(18p)ROMAIN, D. R; DAGGER, P; COLUMBANO-GREEN, L. M et al.Journal of medical genetics. 1992, Vol 29, Num 7, issn 0022-2593, p. 513Article

Three cases of partial trisomy 7q owing to rare structural rearrangements of chromosome 7ROMAIN, D. R; CAIRNEY, H; STEWART, D et al.Journal of medical genetics. 1990, Vol 27, Num 2, pp 109-113, issn 0022-2593, 5 p.Article

Bloom syndrome and maternal uniparental disomy for chromosome 15WOODAGE, T; MADHURI PRASAD; TRENT, R. J et al.American journal of human genetics. 1994, Vol 55, Num 1, pp 74-80, issn 0002-9297Article

t(2;14)(q23;q32.3) as the sole abnormality in a patient with acute nonlymphocytic leukemia (FAB-M4)COLUMBANO-GREEN, L. M; ROMAIN, D. R; CARTER J et al.Cancer genetics and cytogenetics. 1990, Vol 48, Num 2, pp 255-257, issn 0165-4608, 3 p.Article

Studies on three rare fragile sites: 2q13, 12q13, and 17p12 segregating in one familyROMAIN, D. R; COLUMBANO-GREEN, L. M; SMYTHE, R. H et al.Human genetics. 1986, Vol 73, Num 2, pp 164-170, issn 0340-6717Article

Direct intrachromosomal duplication of 16q and heritable fragile site fra (10) (q25) in the same patientROMAIN, D. R; FRAZER, A. G; COLUMBANO-GREEN, L. M et al.American journal of medical genetics. 1984, Vol 19, Num 3, pp 507-513, issn 0148-7299Article

Familial distal trisomy 8(q24.13→qter)ROMAIN, D. R; BLOXHAM, R. A; COLUMBANO-GREEN, L. M et al.Journal of medical genetics. 1989, Vol 26, Num 2, pp 133-138, issn 0022-2593Article

Partial monosomy 12 p 13.1→13.3ROMAIN, D. R; GOLDSMITH, J; COLUMBANO-GREEN, L. M et al.Journal of medical genetics. 1987, Vol 24, Num 7, pp 434-436, issn 0022-2593Article

A complex structural rearrangement of chromosome 4 in a woman without phenotypic features of Wolf-Hirschhorn syndromeROMAIN, D. R; COLUMBANO-GREEN, L. M; PARFITT, R. G et al.Clinical genetics. 1985, Vol 28, Num 2, pp 166-172, issn 0009-9163Article

Partial trisomy 14q 24→q terROMAIN, D. R; COLUMBANO GREEN, L. M; SMYTHE, R. H et al.Journal of medical genetics. 1983, Vol 20, Num 6, pp 466-467, issn 0022-2593Article

Molecular studies of translocations and trisomy involving chromosome 13ROBINSON, W. P; BERNASCONI, F; DUTLY, F et al.American journal of medical genetics. 1996, Vol 61, Num 2, pp 158-163, issn 0148-7299Article

Partial trisomy fo 2q in a patient with dir dup(2)-q33.1q35ROMAIN, D. R; MACKENZIE, N. G; MOSS, D et al.Journal of medical genetics. 1994, Vol 31, Num 8, pp 652-653, issn 0022-2593Article

A rae heteromorphism of chromosome 20 and reproductive lossROMAIN, D. R; WHYTE, S; CALLEN, D. F et al.Journal of medical genetics. 1991, Vol 28, Num 7, pp 477-478, issn 0022-2593Article

Partial monosomy for chromosome 22 in a patient with del(22)(pter → q13.1::q13.33 → qter)ROMAIN, D. R; GOLDSMITH, J; CAIRNEY, H et al.Journal of medical genetics. 1990, Vol 27, Num 9, pp 588-589, issn 0022-2593, 2 p.Article

Mosaicism with a normal cell line and an autosomal structural rearrangementGARDNER, R. J. M; DOCKERY, H. E; FITZGERALD, P. H et al.Journal of medical genetics. 1994, Vol 31, Num 2, pp 108-114, issn 0022-2593Conference Paper

Late replication studies and esterase D levels in a case of unbalanced X; autosome translocation, 46, X, t(X; 13) (q27; q12)ROMAIN, D. R; COLUMBANO-GREEN, L. M; PARFITT, R. G et al.Journal of medical genetics. 1988, Vol 25, Num 10, pp 716-718, issn 0022-2593Article

Two cases of ring chromosome 11ROMAIN, D. R; GEBBIE, O. B; PARFITT, R. G et al.Journal of medical genetics. 1983, Vol 20, Num 5, pp 380-382, issn 0022-2593Article