British medical genetics conferenceJournal of medical genetics. 1995, Vol 32, Num 2, pp 135-155, issn 0022-2593Conference Proceedings

Leber's hereditary optic neuropathy : the clinical relevance of different mitochondrial DNA mutationsRIORDAN-EVA, P; HARDING, A. E.Journal of medical genetics. 1995, Vol 32, Num 2, pp 81-87, issn 0022-2593Conference Paper

Genomic rearrangements in childhood spinal muscular atrophy : linkage disequilibrium with a null alleleDANIELS, R. J; CAMPBELL, L; RODRIGUES, N. R et al.Journal of medical genetics. 1995, Vol 32, Num 2, pp 93-96, issn 0022-2593Conference Paper

Molecular cytogenetic characterisation of a small ring X chromosome in a Turner patient and in a male patient with congenital abnormalities : role of X inactivationCALLEN, D. F; EYRE, H. J; DOLMAN, G et al.Journal of medical genetics. 1995, Vol 32, Num 2, pp 113-116, issn 0022-2593Conference Paper

Cowden syndromeHANSSEN, A. M. N; FRYNS, J. P.Journal of medical genetics. 1995, Vol 32, Num 2, pp 117-119, issn 0022-2593Conference Paper

DNA analysis of Huntington's disease in southern ChineseCHAN, V; YU, Y. L; CHAN, T. P. T et al.Journal of medical genetics. 1995, Vol 32, Num 2, pp 120-124, issn 0022-2593Conference Paper

Recurrence risk for germinal mosaics revisitedVAN DER MEULEN, M. A; VAN DER MEULEN, M. J. P; TE MEERMAN, G. J et al.Journal of medical genetics. 1995, Vol 32, Num 2, pp 102-104, issn 0022-2593Conference Paper

The prenatal exclusion test for Huntington's disease : experience in the west of Scotland, 1986-1993TOLMIE, J. L; DAVIDSON, H. R; MAY, H. M et al.Journal of medical genetics. 1995, Vol 32, Num 2, pp 97-101, issn 0022-2593Conference Paper