Microsoft Word - HHE00IBF.rtf Special Section Hum. Hered. 1980;30:I-VI Contents, Vol. 30, 1980 Founded 1950 as ‘Acta Genetica et Statistica Medica’ by Gunnar Dahlberg Editors: M. Hauge, Odense L. Beckman, Umeå Editorial Board: L. Gedda, Rome R. Grubb, Lund K. Henningsen, København D. Klein, Geneve T. Larsson, Stockholm H. Lehmann, Cambridge Margareta Mikkelsen, København J. Mohr, København A. E. Mourant, London H. Nachtsheim, Berlin J. V. Neel, Ann Arbor, Mich. P. O. Pedersen, København Marianne Rasmuson, Umeå S. Refsum, Oslo L. D. Sanghvi, Bombay M. Siniscalco, Napoli T. Sjörgen, Göteborg E. T. O. Slater, London A. C. Stevenson, Oxford E. Strömgren, Risskov R. Turpin, Paris F. Vogel, Heidelberg M.Whittacker, Exeter A. C. Allison, Harrow A. G. Beam, New York, N.Y K. Berg, Oslo J. A. Book, Uppsala L. L. Cavalli-Sforza, Stanford, Calif. T. J. David, Manchester E. Essen-Möller, Lysekil F. C. Fraser, Montreal J. A. Fraser Roberts, London N. Freire-Maia, Curitiba J. 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S.KargerAG, P.O.Box,4009 Basel (Switzerland) Printed in Switzerland by Buchdruckerei National-Zeitung + Basler Nachrichten AG, Basel Contents Vol. 30,1980 No. 1 Original Paper Alpha-1-Antitrypsin Phenotypes in French Canadian Newborns Joly, J.; Richer, G.; Boisvert, F., and Laverdière, M 1 Survey on Haemoglobin Variants, ß-Thalassaemia, Glucose-6-Phosphate Dehydrogenase Deficiency and Haptoglobin Types in Turkish People Living in Manavgat, Serik and Boztepe (Antalya) Aksoy, M.; Dinçol, G., and Erdem, S 3 Interaction of Sickle Cell Trait and Glucose-6-Phosphate Dehydrogenase Deviciency in Cameroon Bernstein, S.C.; Bowman, J.E., and Kaptue Noche, L 7 Transferrin, Haptoglobin and Group-Specific Component Types in Tribal Populations of Andhra Pradesh Goud, J. D. and Rao, P.R 12 The’ 18’ Variant of Human Placental Alkaline Phosphatase is Identical to the ‘D-Variant’ Doellgast, G.J.; Kennedy, M., and Donald, L.J 18 Sjögren-Larsson Syndrome in Dizygous Twin Sisters David, TJ 21 Human Red Cell Galactose-1 -Phosphate Uridylyltransferase (EC 2.7.7.12). Electrophoretically Determined Polymorphism in Denmark and Its Use in Paternity Cases Eriksen, B. and Dissing, J 27 Genetic Studies of Red Cell Glutamic-Pyruvic Transaminase in Some Japanese Populations Nishigaki, I.; Itoh, T.; Suzuki, H., and Fujiki, N 33 Properdin Factor B Polymorphism in Afghanistan Benkmann, H.G.;Goedde, H.W.;Agarwal, D.P.;Flatz, G.;Rahimi, A.;Kaifie, S., andDelbrück, H.... 39 Haptoglobin Types in Breast Carcinoma Tsamantanis, C; Delinassions, J.G.; Kottaridis, S., and Christodoulou, C 44 C3 Polymorphism in Patients with Chronic Uremia Stoffersen, E. and Jørgensen, K.A 46 Hemoglobin New York Associated with Alpha-Thalassemia Kendalí, A. and Pang, W 50 GPT Polymorphism in the Population of Bologna and Linkage Analysis with Beta-Thalassaemia Facchini, F.; Gruppioni, G.; Veronesi-Martuzzi, F., and Zannotti, M 54 A Further Report on a Kindred with Cases of 4p Trisomy and Monosomy Mortimer, J.G.; Chewings, W.E., and Gardner, RJ.M 58 Association of Glyoxalase I Allotypes with Graves’ Disease and Diabetes mellitus Moens, H.; Payne, R.; Carter, N.D., and Farid, N.R 62 No. 2 Original Paper Twin Studies and Substrate Differences in Platelet Monoamine Oxidase Activity Hussein, L.; Sindarto, E., and Goedde, H.W 65 Use of Multiple Logistic Analysis in Twin Zygosity Diagnosis Sarna, S. and Kaprio, J 71 Serum Levels of Alpha-1-Antitrypsin in Individuals with Different Pi M Subtypes Beckman, G. and Beckman, L 81 IV Contents Duplication of Region 2q31 →2qter in a Family with 2/9 Translocation Howard-Peebles, P.N. and Goldsmith, J.P 84 Determination of Parental Heterozygosity in Dermatoglyphic Characters Bener, A 89 A Population Genetic Study on the Ag Polymorphism in South African Indians and Negroids Hitzeroth, H. W.; Butler, R., and Bütler-Brunner, E 94 A Note on Gene Frequency Estimation with Misclassification Present Selvin, S ‘. 104 Pi Phenotypes in North American Workers: Racial Differences and Comparisons with Reported Frequencies Ashley, M.J.; Chan-Yeung, M, and Corey, P.N 107 Heritability Estimates of Somatotype Components Based upon Familial Data Bouchard, C; Demirjian, A., and Malina, R.M 112 Frequency of Gc Alleles and a Variant Gc Allele in Iceland Karlsson, S.; Arnason, A.; Thordarson, G., and Olaisen, B 119 Different Expressions of One Gene for Congenital Achromatopsia with Amblyopia in Northern Sweden Nordstrom, S. and Polland, W 122 No. 3 Original Paper AlphapAntitrypsin Phenotypes in Northern Sweden Beckman, G.; Beckman, L., and Nordenson, 1 129 Red Cell Glutathione Peroxidase in Various Jewish Ethnic Groups in Israel Golan, R.; Ben Ezzer, J., and Szeinberg, A 136 Comparative Study of Red Cell Enzymes in Mirpur (a Portuguese-Descendant Community) and a Neighbouring Hindu Population of Gopalchak Bharati, P.; Ghosh, A.K.; Dey, B.; Das, S.K.; Roy, M.; Banerjee, S., and Gupta, R 142 Maternal Age and Dermatoglyphic Asymmetry in Man: Another Look Young, R.S. and Reed, T 145 Partial Lipodystrophy and Familial C3 Deficiency McLean, R.H. and Hoefnagel, D 149 Serum IgE Levels in Twins Sistonen, P.; Johnsson, V.; Koskenvuo, M., and Aho, K 155 Mitochondrial Malic Enzyme Polymorphism in an Indian Population Ghosh, U.; Banerjee, P.K., and Saha, N 159 Genetic Characteristics of Hemophilia A in Chile Cruz-Cokem, R. and Rivera, L 161 Study of Red Blood Cell and Serum Enzymes in Five Pyrenean Communities and in a Basque Population Sample Vergnes, H.¦Constans, J.iQuilici, J.C.; Levèvre-Witier, P.; Sevin, J., and Stevens, M 171 Protein and Enzyme Polymorphisms in Affective Disorders in Northern Greece Parisi, H.A.; Lanara, E.C.; Triantaphyllidis, CD 181 Effects of Parental Consanguinity on Mortality and Reproductive Function Lindelius, R. 185 Comparing the ‘Family Set’ Approach to Estimate Heritability with Other Conventional Estimators: a Monte Carlo Simulation Rodriguez, A.; Chakraborty, R., and Schull, W.J 192 Contents V No. 4 Original Paper Is the HpO Phenomenon in Tropical Populations Really Genetic? Rougemont, A.; Quilici, M; Delmont, J., and Ardissone, J.P 201 Some Biochemical Polymorphisms in Members of the Gaddi Tribe of Himachal Pradesh Kaur, H.; Sehajpal, P.K.; Khanna, A.K., and Shrivastava, P.K 204 Isoenzymes of Red Cell Glyoxalase I (EC 4.4.1.5) in a Finnish Population Uotila, L. and Koivusalo, M 207 Polymorphism of the Sixth Component of Complement (C6) in Norwegian Lapps Olving, J.H.; Teisberg, P., and Olaisen, B 211 Search for Linkage between Dermatoglyphic Sole Characters and Blood Groups Bener, A 215 Plasma Protein and Enzyme Polymorphisms in Belgium Brocteur, J.; Hoste, B., and Andre, A 221 Mohr-Wriedt (A2) Brachydactyly. Analysis of a Large Brazilian Kindred Freire-Maia, N.; Maia, N.A., and Pacheco, C.N.A 225 Erythrocyte Glyoxalase I and Esterase D Polymorphisms in Four French Populations Vergnes, H.; Meyer, S.; Weil, D.; Goudemand, J.; Brevière, D.; Sevin, J., and Constans, J 232 Frequencies of Gm and Km Allotypes in the Population of Singapore, Sri Lanka and Punjabis in North India Daveau, M.; Rivat, L.; Lalouel, J.M.; Langaney, A.; Roberts, D.F., and Simons, M.J 237 Polymorphism of the Second Component of Complement (C2) in Graves’ Disease Noel, E.P.; Sampson, L.; Pepper, B.M., and Farid, N.R 245 Electrophoretic Investigation of γ-Glutamyl-Cyclotransferase from Human Erythrocytes Board, P.G 248 Population Studies in Cameroon. Hemoglobin S, Glucose-6-Phosphate Dehydrogenase Deficiency and Falciparum Malaria Bernstein, S.C.; Bowman, J.E., and Kaptue Noche, L 251 Short Communications Glyoxalase I (GLO; EC 4.4.1.5.). Gene Frequency Variation in Iraq Al-Agidi, S.K.; Papiha, S.S., and Shukri, S.M 259 High Frequency of Ina Antigen Among Iranians and Arabs Badakere, S.S.; Vasantha, K.; Bhatia, H.M.; Ala, F.; Clarke, V.A.; Moesri, R.; Sommai, S., and Amin, A.B 262 Book Review 264 No. 5 Original Paper Dermatoglyphic Traits in an Amish-Mennonite Population in Ontario Tutton, D.A. and Zachariah, K 265 Glucose-6-Phosphate Dehydrogenase in an Afro-American Population Calvert, A.F. and Trimble, G.E 271 A Note on the Frequency of Consanguineous Marriages in Reading, England in 1972/1973 Coleman, D.A 278 Properdin Factor B (Bf) as an Exclusion Determinate in Parentage Testing Dykes, D. and Polesky, H 286 VI Contents Genetic Studies on the Chenchu Tribe of Andhra Pradesh, India Ramesh, A.; Blake, N.M.; Vijayakumar, M., and Murty, J.S 291 Alpha-1 -Antitrypsin Types and Chronic Obstructive Lung Disease in an Industrial Community in Northern Sweden Beckman, G.; Beckman, L.; Mikaelsson, B.; Rudolphi, O.; Stjernberg, N., and Wiman, L.-G 299 Variations on Dermal Ridges in Nine Population Groups of Maharashtra, India. I. Intra- and Interpopulation Diversity Malhotra, K.C.; Chakraborty, R.; Bhanu, B.V., and Fulmali, P.M 307 Transferrin C Subtypes and Spontaneous Abortion Beckman, G.; Beckman, L., and Sikström, C 316 Probability Calculations in Pedigrees under Complex Modes of Inheritance Lalouel, J.M 320 ß + -Thalassemia Intermedia. Genetic and Biochemical Study of a Family Including 3 Cases Philip, T.; Souillet, G.; Philippe, N.; Freycon, F.; Bektas, S.; Morlé, L.; Trabuchet, G., and Godet, J. 324 Short Communication Distribution of ABO and Rh (D) Blood Groups among Four Endogamous Groups of Andhra Pradesh Reddi, A.P.; Mukherjee, B.N., and Ramachandraiah, T 331 No. 6 Original Paper A New Unstable PI M Variant of dp Antitrypsin in a Finnish Isolate Frants, R.R. and Eriksson, A.W 333 Studies on the Immunoglobulin Allotypes of Asiatic Populations. VIII. Immunoglobulin Allotypes among the Tuvinians of the USSR Schanfield, M.S.; Alexeyeva, T.E., and Crawford, M.H 343 Segregation Analysis of Schizophrenia under a Mixed Genetic Model Carter, C.L. and Chung, C.S 350 Slow-Moving Serum Albumin Variant in a South Indian Tribal Population Walter, H.; Veerraju, P., and Hilling, M 357 Glucose-6-Phosphate Dehydrogenase Deficiency in South Vietnamese Panich, V.; Bumrungtrakul, P.; Jitjai, C; Kamolmatayakul, S.; Khoprasert, B.; Klaisuvan, C; Kongmuang, U.; Maneechai, P.; Pornpatkul, M.; Ruengrairatanaroje, P.; Surapruk, P.; and Viriyayudhakorn, S 361 Dermatoglyphic Peculiarities in Hypospadias Micle, S. and Fried, K 365 Absent dTriradius and Dotting of the Ridges in Siblings Wertelecki, W.; Plato, C, and Plato, C.C 368 Heritable Salivary Proteins and Dental Disease Friedman, R.D.; Azen, E.A.; Yu, P.L.; Green, P.A.; Karn, R.C., and Merritt, A.D 372 Transferrin C Subtypes in US Blacks and Whites Kueppers, F. and Harpel, B.M 376 Short Communication GLO Polymorphism in Iceland Karlsson, S.; Arnason, A., and Jensson, Ó 383 Announcements 386 Author Index 387 Subject Index 389