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Alcaptonuria: Una famiglia con dominanza irregolare

Published online by Cambridge University Press:  01 August 2014

L. Romei  and
L. Braconi
L. Romei
Affiliation:
Istituto di Genetica Medica e Gemellologia, “G. Mendel”
L. Braconi
Affiliation:
Istituto di Genetica Medica e Gemellologia, “G. Mendel”

Abstract

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Type
Research Article
Information
Acta geneticae medicae et gemellologiae: twin research , Volume 9 , Issue 1 , January 1960 , pp. 103 - 107
Copyright
Copyright © The International Society for Twin Studies 1960

References

Bibliografia

1. Bagnal, E. S.: New England Journ. Med., 201; 422; 1929.Google Scholar
2. Barondes, R.: Alkaptonuria: unusual case with arthralgia, purpura and glomerulonephritis. Milit. Surg., 113 (2); 91; 1953.Google Scholar
3. Beadle, G. W. & Tatum, E. L.: Genetic control of biochemical reactions in Neurospora. Proc. Nat. Acad. Sci., 27; 499; 1941.Google Scholar
4. Black, R. L. & Lowney, J. F. & Duff, J. A.: Alkaptonuria and Ochronosis: report of five cases in an American family. A.M.A. Arch. inter. Medic., :3 (1); 7586; 1954.Google Scholar
5. Ceconi, A.: Medicina interna. Ed. Minerva Med. Vol. IV; 435; 1933.Google Scholar
6. De Benedetti, & D'Anelli, : Epicrisi di un caso di alcaptonuria familiare. Il Policlinico Sez. prat.Google Scholar
7. De Grouchy, J.: L'hérédité moléculaire. Ed. Istituto Mendel Roma, 1958.Google Scholar
8. Dent, C. E. & Philpott, G. R.: The lancet, 1; 182; 1954.Google Scholar
9. Embden, H. Z.: Phys. Chem., 17; 182; 1893.Google Scholar
10. Falta, W.: Deutsch. Ark. Klin. Med., 81; 231; 1904.Google Scholar
11. Garrod, A. E.: Incidence of Alkaptonuria. The Lancet 2; 1616; 1902.CrossRefGoogle Scholar
12. Garrod, A. E.: Inborn errors of Metabolism. Frowde, Hodder, Stoughton London 1923.Google Scholar
13. Gates, R. R.: Human Genetics. McMillan NY. 1946.Google Scholar
14. Goldston, M. & Steele, J. M. & Dobriner, K.: Alkaptonuria and Ochronosis, with a report of 3 p. and metabolic studies in 2. Am. Med., 13 (14); 432; 1952.Google Scholar
15. Hall, W. K., Howkins, K. R. & Child, G. P.: The inheritance of Alkaptonuria. Journ. of Heredity, 41; 23: 1950.CrossRefGoogle Scholar
16. Harris, H.: Genes and enzimes in man. Delle Leggi Mendeliane. Ed. Istituto Mendel, Roma 206; 1955.Google Scholar
17. Hogber, L., Worrall, R. L. & Zieve, I.: The genetic basis of Alkaptonuria. Proc. Roy. Soc. Ed., 52; 264; 1932.Google Scholar
18. Langar, & Lieb, : citati da Ceconi.Google Scholar
19. La Du, B. N. & Zannoni, : Jour. Biol. Chem., 219; 273; 1956.Google Scholar
20. Leaf, G. & Neuberger, A.: Bioch. Jour. 43; 606. 1948.Google Scholar
21. Mateika, : Citato da Ceconi.Google Scholar
22. Matsunaga, E. & Murata, T.: Two cases of phenilketonuria in Japanese. The Japanese Jour. Hum. Gen. v. 4; 2, 3; 154; 1959.Google Scholar
23. Milch, R. A. & Milch, H.: Dominant inheritance of alcaptonuria. Acta Genet., 7; 178; 1957.Google Scholar
24. Neuberger, A., Rimington, C., Wilson, J. M.: Bioch. Jour., 41; 438; 1947.Google Scholar
25. Oppenheimer, B. & Kline, B.: Arch. of Inter. Med., 29; 732; 1922.Google Scholar
26. Pieter, H.: Une famille d'alcaptonuriques. Presse Med., 33; 1310; 1925.Google Scholar
27. Toenniessen, E.: Ueber die Vererbung der Alkaptonuria des Menschen. Zeit. f. Abst. und Vererb. 29; 26; 1922.Google Scholar