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  Bergen (ioi): LITE: Human Heredity Vol. 46, No. 3, 1996  

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To: Multiple recipients of list HUM-MOLGEN <HUM-MOLGEN@NIC.SURFNET.NL>
Subject: LITE: Human Heredity Vol. 46, No. 3, 1996
From: "Bergen (ioi)" <A.A.Bergen@AMC.UVA.NL>
Date: Tue, 2 Apr 1996 13:48:15 +0200

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
        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.

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. 


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