Waardenburg syndrome and Hirschsprung disease: evidence for pleiotropic effects of a single dominant gene.
暂无分享,去创建一个
[1] S. Arias,et al. Probable loose linkage between the AB0 locus and Waardenburg syndrome type I , 1975, Humangenetik.
[2] W. M. Layton,et al. Genetics, chance, and morphogenesis. , 1987, American journal of human genetics.
[3] M. Lyon,et al. Chromosome maps of man and mouse, III. , 1987, Genomics.
[4] M. Hultén,et al. Homozygosity in piebald trait. , 1987, Journal of Medical Genetics.
[5] T. P. Rothman,et al. Inability of neural crest cells to colonize the presumptive aganglionic bowel of ls/ls mutant mice: Requirement for a permissive microenvironment , 1987, The Journal of comparative neurology.
[6] J. C. Law,et al. Hirschsprung disease: a genetic study , 1985, Clinical genetics.
[7] P. Lane,et al. Association of megacolon with a new dominant spotting gene (Dom) in the mouse. , 1984, The Journal of heredity.
[8] L. Ambani. Waardenburg and Hirschsprung syndromes. , 1983, The Journal of pediatrics.
[9] M. Gadd,et al. Hirschsprung's disease in a kindred: a possible clue to the genetics of the disease. , 1982, Journal of pediatric surgery.
[10] K. Shah,et al. White forelock, pigmentary disorder of irides, and long segment Hirschsprung disease: possible variant of Waardenburg syndrome. , 1981, The Journal of pediatrics.
[11] N E Morton,et al. Complex segregation analysis with pointers. , 1981, Human heredity.
[12] A. Mahakrishnan,et al. Piebaldness with Hirschsprung's disease. , 1980, Archives of dermatology.
[13] G. Omenn,et al. The association of Waardenburg syndrome and Hirschsprung megacolon. , 1979, American journal of medical genetics.
[14] J. Ott. Estimation of the recombination fraction in human pedigrees: efficient computation of the likelihood for human linkage studies. , 1974, American journal of human genetics.
[15] N E Morton,et al. Analysis of family resemblance. 3. Complex segregation of quantitative traits. , 1974, American journal of human genetics.
[16] W. Webster. Embryogenesis of the enteric ganglia in normal mice and in mice that develop congenital aganglionic megacolon. , 1973, Journal of embryology and experimental morphology.
[17] E. Passarge. The genetics of Hirschsprung's disease. Evidence for heterogeneous etiology and a study of sixty-three families. , 1967, The New England journal of medicine.
[18] M. Bodian,et al. A family study of Hirschsprung's disease , 1963 .
[19] N. Morton. Sequential tests for the detection of linkage. , 1955, American journal of human genetics.