Skip to main content

. 1993 Sep;30(9):798–799. doi: 10.1136/jmg.30.9.798

Autozygosity mapping, complex consanguinity, and autosomal recessive disorders.

R F Mueller, D T Bishop

PMCID: PMC1016549 PMID: 8411082

798

Selected References

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

Conneally P. M., Heuch I. Letter: A computer program to determine genetic risks: a simplified version of PEDIG (Heuch and Li, 1972). Am J Hum Genet. 1974 Nov;26(6):773–775. [PMC free article] [PubMed] [Google Scholar]
Corey L., Whitley R. J., Stone E. F., Mohan K. Difference between herpes simplex virus type 1 and type 2 neonatal encephalitis in neurological outcome. Lancet. 1988 Jan 2;1(8575-6):1–4. doi: 10.1016/s0140-6736(88)90997-x. [DOI] [PubMed] [Google Scholar]
Darr A., Modell B. The frequency of consanguineous marriage among British Pakistanis. J Med Genet. 1988 Mar;25(3):186–190. doi: 10.1136/jmg.25.3.186. [DOI] [PMC free article] [PubMed] [Google Scholar]
Duyk G., Gastier J. M., Mueller R. F. Traces of her workings. Nat Genet. 1992 Sep;2(1):5–8. doi: 10.1038/ng0992-5. [DOI] [PubMed] [Google Scholar]
Heney D., Mueller R., Turner G., Karbani G., Cadranel J., Lewis I. J., Bailey C. C. Familial microcephaly with normal intelligence in a patient with acute lymphoblastic leukemia. Cancer. 1992 Feb 15;69(4):962–965. doi: 10.1002/1097-0142(19920215)69:4<962::aid-cncr2820690421>3.0.co;2-w. [DOI] [PubMed] [Google Scholar]
Lander E. S., Botstein D. Homozygosity mapping: a way to map human recessive traits with the DNA of inbred children. Science. 1987 Jun 19;236(4808):1567–1570. doi: 10.1126/science.2884728. [DOI] [PubMed] [Google Scholar]
Morton N. E. Genetic epidemiology of hearing impairment. Ann N Y Acad Sci. 1991;630:16–31. doi: 10.1111/j.1749-6632.1991.tb19572.x. [DOI] [PubMed] [Google Scholar]
Shaw N. J., Haigh D., Lealmann G. T., Karbani G., Brocklebank J. T., Dillon M. J. Autosomal recessive hypoparathyroidism with renal insufficiency and developmental delay. Arch Dis Child. 1991 Oct;66(10):1191–1194. doi: 10.1136/adc.66.10.1191. [DOI] [PMC free article] [PubMed] [Google Scholar]
Wong F. L., Cantor R. M., Rotter J. I. Sample-size considerations and strategies for linkage analysis in autosomal recessive disorders. Am J Hum Genet. 1986 Jul;39(1):25–37. [PMC free article] [PubMed] [Google Scholar]

ACTIONS

RESOURCES