Human Heredity: Volume 47, No. 5, 1997

Original Papers

241 The Spectrum of Beta-Thalassaemia Mutations in the Lebanon

250 Angiotensin-Converting Enzyme Deletion Polymorphism Is Associated with Hypertension in a Sikh Population
Mastana, S.; Nunn, J. (Loughborough)

254 Molecular and Cytogenetic Investigations of the Fragile X Region Including the Frax A and Frax E CGG Trinucleotide Repeat Sequences in Families Multiplex for Autism and Related Phenotypes
Gurling, H.M.D. (London); Bolton, P.F. (Cambridge); Vincent, J.; Melmer, G.; Rutter, M. (London)

263 Ethnic Differences in the HFE Codon 282 (Cys/Tyr) Polymorphism
Beckman, L.E. (Umeå); Saha, N. (Singapore); Spitsyn, V. (Moscow); Van Landeghem, G.; Beckman, L. (Umeå)

268 Linkage Analysis of Manic Depression (Bipolar Affective Disorder) in Icelandic and British Kindreds using Markers on the Short Arm of Chromosome 18
Kalsi, G.; Smyth, C. (London); Brynjolfsson, J. (Reykjavik); Sherrington, R.S.; Oâ€™Neill, J.; Curtis, D.; Rifkin, L.; Murphy, P. (London); Petursson, H. (Reykjavik); Gurling, H.M.D. (London)

279 Investigation of Complement C4B Deficiency in Schizophrenia
Schroers, R.; Nöthen, M.M.; Rietschel, M. (Bonn); Albus, M. (Haar); Maier, W.; Schwab, S.; Wildenauer, D.; Fimmers, R.; Propping, P.; Dewald, G. (Bonn)

283 Haptoglobin Polymorphism in Korean Patients with Cardiovascular Diseases
Hong, S.H.; Kang, B.Y.; Lim, J.H. (Seoul); Nankoong, Y. (Kangreung); Oh, M.Y. (Cheju); Kim, J.Q.; Lee, C. C. (Seoul)

288 Paternity Analysis in Cases of Father-Daughter Incest Using Multiallelic Loci
Cifuentes O., L.; Jorquera G., H. (Santiago)

Original Papers

Short Communications