Pericentric inversion in chromosome 2 without phenotypic effect
暂无分享,去创建一个
[1] J. Fryns,et al. Mosaic pericentric inversion of chromosome 2. , 1983, Journal de genetique humaine.
[2] J. Grouchy,et al. Atlas des maladies chromosomiques , 1982 .
[3] F. Salzano,et al. Familial pericentric inversion of chromosome 2. , 1981, Journal de genetique humaine.
[4] R. Tenconi,et al. Study on segregation and risk for abnormal offspring in carriers of pericentric inversion of the (p11←q13) segment of chromosome 2 , 1980 .
[5] G. Sutherland,et al. Chromosome studies at the paediatric necropsy , 1978 .
[6] P. Jacobs,et al. A cytogenetic survey of 11,680 newborn infants , 1974, Annals of human genetics.
[7] O. Hníková,et al. Microdensitometric identification of the pericentric inversion of chromosome No.2 and of duplication of the short arm of chromosome No.7 in a reexamined case. , 1973, Human heredity.