Clinical genetics / edited by Arnold Sorsby.

Date:
1953
Catalogue details

Licence: Attribution-NonCommercial 4.0 International (CC BY-NC 4.0)

Credit: Clinical genetics / edited by Arnold Sorsby. Source: Wellcome Collection.

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    SELECTED BIBLIOGRAPHY Albinism *Bamber, R. C. (1927). Bibl. genet, Lpz-, 3, 1. Harris, R. G. (1926). Amer. J. phys. Anthrop., 9, 17. *Klein, D. (1950). Helv. paediat. acta, 5, 38. McCrachin, R. H. (1937). Amer. J. Dis. Child., 54, 786. Rife, D. C., Schoenfeld, M. D., and Hunstead, M. (1946). J. Hered., Ъ1, 3. Wakefield, E. G., and Dellinger, S. С. (1936). Ann. intern. Med., 9, 1149. Cystine diathesis Abderhalden, E. (1903). Z. phys. Chem., 38, 557. Brooks, W. D. W., Heasman, M. A., and Lovell, R. R. H. (1949). Lancet, 1, 1096. Biirki, E. (1941). Ophthalmologica, 101, 257. Cohn, J. (1899). Beri. ¡clin. Wschr., 36, 503. Creveld, S. van, and Grunbaum, A. (1942). Acta paediat., 29, 183. *Dent, C. E., and Harris, H. (1951). Ann. Eugen. Camb., 16, 60. Fanconi, G. (1945). Helv. paediat. acta, 1, 183. Hottinger, A. (1941). Ann. paediat., 156, 257. — (1942). Ibid., 159, 173. Lewis, H. B. (1932), Ann. intern. Med., 6, 183. Linder, G. С., Bull, G. M., and Grayce, I. (1949). Clin. Proc., 8, 1. Looser, R. (1944). Ann. paediat., 163, 251. Patch, F. S. (1934). Canad. med. Ass. J., 31, 250. Roulet, F. (1941). Ann. paediat., 156, 284. Schleicher, R., and Ostertag, M. (1935). Erbarzt, 2, 105. Ullrich, O. (1948). Z. Kinderheilk., 66, 154. Amyloidosis Ostertag, B. (1950). Z. mensch. Vererb.-и. Konstit.lehre, 30, 105. Gout *Bauer, W., and Klemperer, F. (1949). In Diseases of Metabolism, 2nd ed., pp. 611-656. Ed. by G. G. Duncan. Philadelphia and London; Saunders. Additional references: Lichtwitz, L. (1934). Schweiz, med. Wschr., 64, 261. Smyth, C. J., Cotterman, C. W., and Freyberg, R. H. (1948). J. din. Invest., 27, 749. Stecher, R. M., and Hersh, A. H. (1945). Genetics, 30, 24. Talbott, J. H. (1940). J. din. Invest., 19, 645. Lithiasic diatheses Gram, H. C. (1932). Acta med. scand., 78, 268. *Hanhart, E. (1940). Erbpathologie des Stoffwechsels. In Hb. Erbbiologie des Menschen. Ed. by G. Just. Vol. IV/2, p. 796. Berlin; Springer. Mingers (1945). J. beige d'uroL, 14, 103. Ostertag, M., and Spaich, D. (1936). Erbarzt, 3, 71. Romanow, О. (1935). Beitrag zur Frage der Erbbedingtheit von Nierensteinen. Berlin; Inaug.-Diss. Glycogen disease Hanhart, E. (1946). Arch. Klaus-Stift. Vereb-Forsch., 21, 486. Ziegler, E. (1947). Helv. paediat. acta, 2, 56. Idiopathic spontaneous hypoglycaemia Anderson, R. C., Wright, W. S., Bauer, E. G., and McQuarrie, I. (1950). Amer. J. hum. Genet., 2, 264. Cammidge, P. J., and Howard, H. (1937). Proc. R. Soc. Med., 23, 1341. Hartmann, A., and Jaudon, J. (1937). J. Pediat., 11, 1. Weitz, W. (1936). Die Vererbung Innerer Krankheiten, p. 135. Stuttgart; Enke. Renal glycosuria Falta, W. (1937). Klin. Wschr., 10, 306. Hatlehol, R. (1924). Acta med. scand., suppl. 8, p. 260. Hoist, J. E. (1926). Arch, intern. Med., 38, 279. Houston, J. C. (1951). Ann. Eugen, bond., 15, 293. Johnsson, A. (1922). Acta med. scand., 56, 485. Mentzingen, A. von (1935). Z. menschl. Vererb.-u. Konstit.lehre, 19, 166. Galactosuria Bell, L. S., Blair, W. C., Lindsay, S., and Watson, S. J. (1950). J. Pediat., 36, 427. ♦Donnell, G. N., and Lann, St. N. (1951). Paediatrics, 7, 503. Fanconi, G. (1933). J. Kinderheilk., 138, 1. ♦Townsend, E. H., Mason, H. H., and Strong, P. S. (1951). Paediatrics, 7, 760. 207