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Læknablaðið - 15.02.1983, Blaðsíða 15

Læknablaðið - 15.02.1983, Blaðsíða 15
LÆK.NABLADID 41 Warkentin PI, Teitelbaum SL, Kahn AJ, Brown DM. Successful bone-marrow transplantation for infantile malignant osteopetrosis. N Engl J Med 1980; 302: 701-8. 7) Ballet JJ, Griscelli C, Coutris C, Milhaud G, Maroteaux P. Bone-marrow transplantation in osteopetrosis. The Lancet 1977; 1:26. 8) Johnston CC, Lavy N, Lord T, Vellios F, Merritt AD, Deiss WP. Osteopetrosis. A clinical, gene- tic, metabolic, and morphologic study of the dominantly inherited, benign form. Medicine 1968, Baltimore, 47: 149-67. 9) McKusick VA. »Mendelian Inheritance in Man«, 5th Ed. Baltimore: Johns Hopkins Press, 1978. 10) Birth Defects: Original article series, XV, 1979 International nomenklature of constitutional diseases of bone with bibliography. March of Dimes Birth Defects Foundation, New York, 1979. 11) Loria-Cortés R, Quesada-Calvo E, Cordero- Chavarri C. Osteopetrosis in children. J Pediatr 1977;91:43-7. 12) Magnússon B. Vestur-Skaftfellingar 1703-1966. Prentsmiðjan Leiftur h/f, Reykjavík, 1970-1973. 13) Alper CA, Boenisch T, Watson L. Genetic polymorphism in human glycinerich beta-glyco- protein. J exp Med 1972; 135: 68-80. 14) Teisberg P. High voltage agarose gel electro- phoresis in the study of the C3 polymorphism. Vox Sang 1970; 19:47-56. 15) Constans J, Viau M, Cleve H, Jeager G, Quilici JC, Palison MJ. Analysis of the Gc polymor- phism in human populations by isoelectro- focusing on polyacrylamide geis. Demonstrati- on of subtypes of the Gc1 allele and of additional Gc variants. Hum Genet 1978; 41: 53-60. 16) Árnason A, Jensson Ó, Guðmundsson S. Serum esterases of Icelanders I, A »silent« pseudocho- linesterase gene in an lcelandic family. Clin Genet 1975; 7: 405-12. 17) Ktihnl P, Schwabenland R, Spielmann W. In- vestigations on the polymorphism of glyoxalase I (EC 4.4.1.5) in the population of Hessen, Germany. Hum Genet 1977; 38: 99-106. 18) Kömpf J, Bissbort S, Gussmann S, Ritter H. Polymorphism of red cell glyoxalase 1 (E.C.: 4.4.1.5). A new genetic marker in man. Investig- ation of 169 mother-child combinations. Hu- mangenetik 1975; 27: 141-xx. 19) Swallow DM, Povey S, Harris H. Activity of the »red cell« acid phosphatase locus in other tissues. Ann Hum Genet 1973; 37: 31-xx. 20) Chen S-H, Giblett ER. Polymorphism of soluble glutamicpyruvic transaminase: a new genetic marker in man. Science 1971; 173: 148-9. 21) Harris H, Hopkinson DA, Robson EB, Whitta- ker M. Geneticai studies on a new variant of serum cholinesterase detected by electrophore- sis. Ann Hum Genet 1963: 26: 359-xx. 22) Smithies O. Zone electrophoresis of serum in starch gels: Group variations in the serum proteins of normal human adults. Biochem J 1955;61:529-41. 23) Enell H, Pehrson N. Studies on osteopetrosis, I. Clinica! report of three cases with genetic considerations. Acta paediatrica, Uppsala 1958; 47: 279. 24) Jensson Ó, Árnason A, Skaftadóttir I, Linnet H, Jónmundsson GK, Snorradóttir M. Osteopetro sis Recessiva: Arfgeng marmarabeinveiki. Læknaping, Domus Medica, Reykjavík, 22-25. sept., 1981. 25) Tips RL, Lynch HT. Malignant congenital oste- opetrosis resulting from a consanguineous mar- riage. Acta pædiatrica 1962; 51: 585-8. 26) Horton WA, Schimke RN, Iyama T. Osteope- trosis: Further heterogeneity. Pediatrics 1980; 97: 580-5.

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