Two hundred and tenth meeting of the genetical Society: abstracts, 11th to 13th April 1989, NottinghamHeredity (Edinburgh. Print). 1989, Vol 63, issn 0018-067X, 275-286 [12 p.], 2Conference Proceedings

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

DNA methylation based testing of 450 patients suspected of having Prader-Willi syndromeGILLESSEN-KAESBACH, G; GROSS, S; KAYA-WESTERLOH, S et al.Journal of medical genetics. 1995, Vol 32, Num 2, pp 88-92, 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

A weak association between TH and DRD2 genes and bipolar affective disorder in a Spanish samplePEREZ DE CASTRO, I; SANTOS, J; TORRES, P et al.Journal of medical genetics. 1995, Vol 32, Num 2, pp 131-134, issn 0022-2593Conference Paper

Cholinesterase variants : rapid characterisation by PCR/SSCP and evidence for molecular homogeneityHÖHLER, T; HUNDT, M; RITTNER, C et al.Journal of medical genetics. 1995, Vol 32, Num 2, pp 109-112, issn 0022-2593Conference Paper

Contribution of molecular analyses to the estimation of the risk of congenital myotonic dystrophyCOBO, A. M; POZA, J. J; MARTORELL, L et al.Journal of medical genetics. 1995, Vol 32, Num 2, pp 105-108, issn 0022-2593Conference Paper

Modification of standard proteinase K/phenol method for DNA isolation to improve yield and purity from frozen bloodNILOFER NINA AHMAD; CU-UNJIENG, A. B; DONOSO, L. A et al.Journal of medical genetics. 1995, Vol 32, Num 2, pp 129-130, issn 0022-2593Conference Paper

Pallister-Hall syndrome and McKusick-Kaufmann syndrome : one entity ?UNSINN, K. M; NEU, N; KREJCI, A et al.Journal of medical genetics. 1995, Vol 32, Num 2, pp 125-128, issn 0022-2593Conference Paper