HUM-MOLGEN archive: LITE: Human Heredity Vol. 46, No. 3, 1996

Human Heredity · International Journal of Human and Medical Genetics Tables of Contents Vol. 46, No. 3, 1996 Original Papers 121 Distribution of Composite CYP1A1 Genotypes in Africans, African-Americans and Caucasians Garte, S.J.; Trachman, J.; Crofts, F.; Toniolo, P.; Buxbaum, J.; Bayo, S.; Taioli, E. (New York, N.Y./Bamako) 128 Phenylketonuria in Costa Rica: Preliminary Spectrum of PAH Mutations and Their Associations with Highly Polymorphic Haplotypes Santos, M.; Kuzmin, A.I.; Eisensmith, R.C.; Goltsov, A.A.; Woo, S.L.C.; Barrantes, R.; de Céspedes, C. (San José/Houston, Tex.) 132 Coagulation Factor XIIIA Subtypes in Brazilian Indians Arnold, G.; Kömpf, J.; Salzano, F.M. (Tübingen/Porto Alegre) 136 Molecular Characterization of Erythrocyte Glucose-6- Phosphate Dehydrogenase Deficiency in Al-Ain District, United Arab Emirates Bayoumi, R.A.; Nur-E-Kamal, M.S.A.; Tadayyon, M.; Mohamed, K.K.A.; Mahboob, B.H.; Qureshi, M.M.; Lakhani, M.S.; Awaad, M.O.; Kaeda, J.; Vulliamy, T.J.; Luzzatto, L. (Al-Ain/London) 142 Butyrylcholinesterase Variants (BCHE and CHE2 Loci) Associated with Erythrocyte Acetylcholinesterase Inhibition in Farmers Exposed to Pesticides Fontoura-da-Silva, S.E.; Chautard-Freire-Maia, E.A. (Curitiba) 148 The Codon 31 Polymorphism of the p53-Inducible Gene p21 Shows Distinct Differences between Major Ethnic Groups Birgander, R.; Själander, A.; Saha, N.; Spitsyn, V.; Beckman, L.; Beckman, G. (Umeå/Singapore/Moscow) 155 Sharing at the Major Histocompatibility Complex Affects the Secondary Sex Ratio in Differing Ways Astolfi, P.; Cuccia, M.; Caruso, C.; Favoino, B.; Fazzari, M.; Mantovani, V.; Lulli, P.; Illeni, M.T.; Martinetti, M. (Pavia) Mutation Report 166 2176insC: A Novel Mutation in Exon 13 of the Cystic Fibrosis Gene Savov, A.; Angelicheva, D.; Jordanova, A.; Kremensky, I.; Kalaydjieva, L. (Sofia/Perth) Original Papers 168 A Splicing Mutation in Intron 16 of the Cystic Fibrosis Transmembrane Conductance Regulator Gene, Associated with Severe Disease, Is Common on Reunion Island Bienvenu, T.; Cartault, F.; Lesure, F.; Renouil, M.; Beldjord, C.; Kaplan, J.C. (Paris/Saint Denis/Saint Pierre) 172 Molecular Characterization of G6PD Deficiency in Oman Daar, S.; Vulliamy, T.J.; Kaeda, J.; Mason, P.J.; Luzzatto, L. (Muscat/London) 177 Detection of Four Novel Mutations in the Porphobilinogen Deaminase Gene in French Caucasian Patients with Acute Intermittent Porphyria Puy, H.; Deybach, J.C.; Lamoril, J.; Robreau, A.M.; Nordmann, Y. (Colombes) ========================================================================= S. KARGER AG BASEL Zentrale Werbung ------------------------------------------------------------------------- Medical and Scientific Publishers Verlag fuer Medizin und Naturwissenschaften Editions medicales et scientifiques ------------------------------------------------------------------------- Freddy Brian (061) 306 13 74 E-Mail fbrian@karger.ch ------------------------------------------------------------------------- S. Karger AG Telephone (061) 306 11 11 Allschwilerstrasse 10 Telefax (061) 306 12 34 P.O. Box + Postfach + Case postale E-Mail karger@karger.ch CH-4009 Basel Switzerland + Schweiz + Suisse -------------------------------------------------------------------------