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editorial
. 1977 May;29(3):312–319.

A probable sex difference in some mutation rates.

F Vogel
PMCID: PMC1685321  PMID: 868880

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Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. BITTER K. ERHEBUNGEN ZUR BESTIMMUNG DER MUTATIONSRATE FUER HAEMOPHILIE A UND B IN HAMBURG. Z Mensch Vererb Konstitutionsl. 1963 Dec 17;37:251–268. [PubMed] [Google Scholar]
  2. 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]
  3. Becker P. E. Neues zur Genetik und Klassifikation der Muskeldystrophien. Humangenetik. 1972;17(1):1–22. [PubMed] [Google Scholar]
  4. 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]
  5. CHEESEMAN E. A., KILPATRICK S. J., STEVENSON A. C., SMITH C. A. The sex ratio of mutation rates of sex-linked recessive genes in man with particular reference to Duchenne type muscular dystrophy. Ann Hum Genet. 1958 May;22(3):235–243. doi: 10.1111/j.1469-1809.1958.tb01418.x. [DOI] [PubMed] [Google Scholar]
  6. DIDISHEIM P., FERGUSON J. H., LEWIS J. H. Hemostatic data in relatives of hemophiliacs A and B; evidence for modifying the classical sex-linked recessive hypothesis. AMA Arch Intern Med. 1958 Feb;101(2):347–354. doi: 10.1001/archinte.1958.00260140179027. [DOI] [PubMed] [Google Scholar]
  7. 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]
  8. Francke U., Felsenstein J., Gartler S. M., Nyhan W. L., Seegmiller J. E. Answer to criticism of Morton and Lalouel. Am J Hum Genet. 1977 May;29(3):307–311. [PMC free article] [PubMed] [Google Scholar]
  9. HALDANE J. B. Mutation in the sex-linked recessive type of muscular dystrophy; a possible sex difference. Ann Hum Genet. 1956 May;20(4):344–347. doi: 10.1111/j.1469-1809.1955.tb01289.x. [DOI] [PubMed] [Google Scholar]
  10. Herrmann J. Der Einfluss des Zeungungsalters auf die Mutationen zu Hämophilie A. Humangenetik. 1966;3(1):1–16. doi: 10.1007/BF00273014. [DOI] [PubMed] [Google Scholar]
  11. 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]
  12. 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]
  13. Morton N. E., Crow J. F., Muller H. J. AN ESTIMATE OF THE MUTATIONAL DAMAGE IN MAN FROM DATA ON CONSANGUINEOUS MARRIAGES. Proc Natl Acad Sci U S A. 1956 Nov;42(11):855–863. doi: 10.1073/pnas.42.11.855. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Morton N. E., Lalouel J. M. Genetic epidemiology of Lesch-Nyhan disease. Am J Hum Genet. 1977 May;29(3):304–311. [PMC free article] [PubMed] [Google Scholar]
  15. NILSSON I. M., BLOMBACK M., THILEN A., FRANCKEN I. V. Carriers of hemophilia A: a laboratory study. Acta Med Scand. 1959 Dec 5;165:357–370. [PubMed] [Google Scholar]
  16. STEVENSON A. C. Muscular dystrophy in Northern Ireland, I. An account of the condition in fifty-one families. Ann Eugen. 1953 Jun;18(1):50–contd. doi: 10.1111/j.1469-1809.1952.tb02497.x. [DOI] [PubMed] [Google Scholar]
  17. STEVENSON A. C. Muscular dystrophy in Northern Ireland. IV. Some additional data. Ann Hum Genet. 1958 May;22(3):231–234. doi: 10.1111/j.1469-1809.1958.tb01417.x. [DOI] [PubMed] [Google Scholar]
  18. Searle A. G. Spontaneous frequencies of point mutations in mice. Humangenetik. 1972;16(1):33–38. doi: 10.1007/BF00393982. [DOI] [PubMed] [Google Scholar]
  19. VOGEL F. Gedanken über den Mechanismus einiger spontaner Mutationen beim Menschen. Z Mensch Vererb Konstitutionsl. 1958;34(4):389–399. [PubMed] [Google Scholar]
  20. 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]
  21. Vogel F. Sind die Mutationsraten für die X-chromosomal recessiven Hämophilieformen in Keimzellen von Frauen niedriger als in Keimzellen von Männern? Humangenetik. 1965;1(3):253–263. doi: 10.1007/BF00395656. [DOI] [PubMed] [Google Scholar]
  22. WALTON J. N., RACE R. R., PHILIP U. On the inheritance of muscular dystrophy; with a note on the blood groups, and a note on colour vision and linkage studies. Ann Hum Genet. 1955 Aug;20(1):1–38. doi: 10.1111/j.1469-1809.1955.tb01274.x. [DOI] [PubMed] [Google Scholar]

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