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Journal of Medical Genetics logoLink to Journal of Medical Genetics
. 1986 Feb;23(1):32–34. doi: 10.1136/jmg.23.1.32

Autosomal recessive or sex linked recessive: a counselling dilemma.

I D Young, Z Nugent, T Grimm
PMCID: PMC1049537  PMID: 3950934

Abstract

This paper discusses the difficult problem that arises when information is sought by female relatives of two or more brothers, each of whom has an identical but undiagnosed or 'new' syndrome, which is likely to be either autosomal recessive or sex linked recessive in inheritance. It is proposed that standard Bayesian methods may be applied in this situation thus incorporating the prior probability for each event with conditional probabilities based upon pedigree analysis.

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Selected References

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

  1. 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]
  2. Harris D. J., Ashcraft K. W., Beatty E. C., Holder T. M., Leonidas J. C. Natal teeth, patent ductus arteriosus and intestinal pseudo-obstruction: a lethal syndrome in the newborn. Clin Genet. 1976 May;9(5):479–482. doi: 10.1111/j.1399-0004.1976.tb01600.x. [DOI] [PubMed] [Google Scholar]

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