Paternal or maternal origin of human i(Xq) isochromosomes

Summary We present a method to test if the proportion of 45,X cases resulting from loss of the maternal chromosome or of cases of 46,X,i(Xq) with the isochromosome of maternal origin is different from 1/2. The available data are consistent with the hypothesis that the normal X present in i(Xq) patients originates with equal probabilities in the fathers and mothers of the patientsThis paper was supported in part by grants from Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP) and Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)