Trisomy 22. Two new cases and delineation of the phenotype.
暂无分享,去创建一个
[1] B. Crandall,et al. Probable trisomy 22 identified by fluorescent and trypsin-giemsa banding. , 1973, Annales de genetique.
[2] J. Scheres. Human chromosome banding. , 1972, Lancet.
[3] K. Gustavson,et al. Three non‐mongoloid patients of similar phenotype with an extra G‐like chromosome , 1972, Clinical genetics.
[4] K. Hirschhorn,et al. Trisomy 22: a clinical entity. , 1971, The Journal of pediatrics.
[5] N. Sadan,et al. The question of trisomy 22 syndrome. , 1971, The Journal of pediatrics.
[6] T. Caspersson,et al. Differential binding of alkylating fluorochromes in human chromosomes. , 1970, Experimental cell research.
[7] M. Mikkelsen,et al. Additional small acrocentric chromosome: two cases. , 2008, Journal of mental deficiency research.
[8] I. Uchida,et al. Familial occurrence of trisomy 22. , 1968, American journal of human genetics.
[9] G. J. Cunningham,et al. VENTILATION OF OPERATING-THEATRES. , 1964, Lancet.
[10] B. Hall. Mongolism and Other Abnormalities in a Family with Trisomy 21–22 Tendency , 1963, Acta paediatrica. Supplementum.
[11] H. Zellweger,et al. Two cases of multiple malformations with an autosomal chromosomal aberration- partial trisomy D? , 1962, Helvetica paediatrica acta.