Full text
PDFSelected References
These references are in PubMed. This may not be the complete list of references from this article.
- Barrai I., Cann H. M., Cavalli-Sforza L. L., De Nicola P. The effect of parental age on rates of mutation for hemophilia and evidence for differing mutation rates for hemophilia A and B. Am J Hum Genet. 1968 May;20(3):175–196. [PMC free article] [PubMed] [Google Scholar]
- Biggs R., Rizza C. R. The sporadic case of haemophilia A. Lancet. 1976 Aug 28;2(7983):431–433. doi: 10.1016/s0140-6736(76)92523-x. [DOI] [PubMed] [Google Scholar]
- Crawhall J. C., Henderson J. F., Kelley W. N. Diagnosis and treatment of the Lesch-Nyhan syndrome. Pediatr Res. 1972 May;6(5):504–513. doi: 10.1203/00006450-197205000-00004. [DOI] [PubMed] [Google Scholar]
- Francke U., Felsenstein J., Gartler S. M., Migeon B. R., Dancis J., Seegmiller J. E., Bakay F., Nyhan W. L. The occurrence of new mutants in the X-linked recessive Lesch-Nyhan disease. Am J Hum Genet. 1976 Mar;28(2):123–137. [PMC free article] [PubMed] [Google Scholar]
- KOSOWER N., CHRISTIANSEN R., MORTON N. E. Sporadic cases of hemophilia and the question of a possible sex difference in mutation rates. Am J Hum Genet. 1962 Jun;14:159–169. [PMC free article] [PubMed] [Google Scholar]
- MORTON N. E., CHUNG C. S. Formal genetics of muscular dystrophy. Am J Hum Genet. 1959 Dec;11:360–379. [PMC free article] [PubMed] [Google Scholar]
- MORTON N. E. Segregation analysis in human genetics. Science. 1958 Jan 10;127(3289):79–80. doi: 10.1126/science.127.3289.79. [DOI] [PubMed] [Google Scholar]
- Roses A. D., Roses M. J., Miller S. E., Hull K. L., Jr, Appel S. H. Carrier detection in Duchenne muscular dystrophy. N Engl J Med. 1976 Jan 22;294(4):193–198. doi: 10.1056/NEJM197601222940404. [DOI] [PubMed] [Google Scholar]
- Seegmiller J. E. Inherited deficiency of hypoxanthine-guanine phosphoribosyltransferase in X-linked uric aciduria (the Lesch-Nyhan syndrome and its variants). Adv Hum Genet. 1976;6:75–163. doi: 10.1007/978-1-4615-8264-9_2. [DOI] [PubMed] [Google Scholar]
- Vogel F., Rathenberg R. Spontaneous mutation in man. Adv Hum Genet. 1975;5:223–318. doi: 10.1007/978-1-4615-9068-2_4. [DOI] [PubMed] [Google Scholar]