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virtual library in human genetics and molecular biology
J.Ott, New York, N.Y.
Associate Editors
L. Beckman, Umea
M. Boehnke, Ann Arbor, MI
C.R. Cloninger, St. Louis, MO
P.M. Conneally, Indianapolis, IN
L.P. ten Kate, Amsterdam
Editorial Board
K. Berg, Oslo
L.L. Cavalli-Sforza, Stanford, CA
A. de la Chapelle, Helsinki
J. Dausset, Paris
T.J. David, Manchester
B. Dutrillaux, Paris
F.C. Fraser, Montreal
N. Freire-Maia, Curitiba
J. Frézal, Paris
R. Grubb, Lund
P.A. Jacobs, Salisbury
P.J. McAlpine, Winnipeg
Margareta Mikkelsen, København
F. Mitelman, Lund
N.E. Morton, Southampton
J. Mohr, København
A.E. Mourant, London
J.V. Neel, Ann Arbor, MI
U. Pettersson, Uppsala
Marianne Rasmuson, Umea
D.L. Rimoin, Los Angeles, CA
L.D. Sanghvi, Bombay
M. Siniscalco, Sassari
F. Vogel, Heidelberg
D.J. Weatherall, Oxford
R.L. White, Salt Lake City, UT
M. Whittaker, Exeter
S. Karger AG, Basel - Switzerland
Original Papers
1 Genetic and Environmental Effects on Urinary Kallikrein, Catecholamines, Sodium, Potassium, Urea Nitrogen and Inorganic Sulfate Sulfur Levels in School-Age Twins
Kagamimori, S.; Naruse, Y.; Matsubara, I.; Li Fu, B.; Sokejima, S.; Yamagami, T. (Toyama)
7 Asian Hypersusceptibility to Motion Sickness
Stern, R.M.; Hu, S.; Uijtdehaage, S.H.J.; Muth, E.R.; Xu, L.H.; Koch, K.L. (University Park, Pa./Hershey, Pa.)
15 Alpha-Thalassemia Genes in Israel: Deletional and Nondeletional Mutations in Patients of Various Origins
Shalmon, L.; Kirschmann, C.; Zaizov, R. (Petah Tikva)
20 Comparison of Single-Entry and Double-Entry Two-Step Couple Screening for Cystic Fibrosis Carriers
ten Kate, L.P.; Verheij, J.B.G.M.; Wildhagen, M.F.; Hilderink, H.B.M.; Kooij, L.; Verzijl, J.G.; Habbema, J.D.F. (Amsterdam/Groningen/Rotterdam)
26 Detection of the Plasma Cholinesterase K Variant by PCR Using an Amplification-Created Restriction Site
Jensen, F.S.; Nielsen, L.R.; Schwartz, M. (Copenhagen)
32 Genetic Epidemiology of the Mitsuda Reaction in Leprosy
Feitosa, M.; Krieger, H.; Borecki, I.; Beiguelman, B.; Rao, D.C. (Rio de Janeiro/St. Louis, Mo./São Paulo/Campinas)
36 Novel Mutation Identified in the PAH Gene
Charikova, E.V. (Moscow)
41 p53 Polymorphisms and Haplotypes Show Distinct Differences between Major Ethnic Groups
Själander, A.; Birgander, R.; Saha, N.; Beckman, L.; Beckman, G. (Umeå/Singapore)
49 p53 Polymorphisms and Haplotypes in Nasopharyngeal Cancer
Birgander, R.; Själander, A.; Zhou, Z.; Fan, C.; Beckman, L.; Beckman, G. (Umeå/Zunyi)
Short Communications
55 Lod Score Curves for Phase-Unknown Matings
Hulbert-Shearon, T.; Boehnke, M.; Lange, K. (Ann Arbor, Mich.)
58 BaII and MspI Polymorphisms of the Dopamine D3 Receptor Gene in African Blacks and Caucasians
Crocq, M.-A.; Buguet, A.; Bisser, S.; Burgert, E.; Stanghellini, A.; Uyanik, G.; Dumas, M.; Macher, J.-P.; Mayerova, A. (Rouffach/La Tronche/Limoges/Freiburg/Brazzaville)
HUMAN HEREDITY (ISSN 0001-5652) is published 6 times annually by S.Karger AG, P.O. Box, CH-4009 Basel. © Copyright 1995 by S.Karger AG
Founded 1950 as 'Acta Genetica et Statistica Medica' by Gunnar Dahlberg. Continued by M. Hauge (1965-1983)
S. KARGER AG BASEL
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