Harris D J, Begleiter M L, Chamberlin J, Hankins L, Magenis R E
Am J Hum Genet. 1982 Jan;34(1):125-33.
A family with three children with trisomy 21 in which the mother is a phenotypically normal, trisomy 21/normal mosaic was studied. Chromosome 21 fluorescent heteromorphisms were used to document that two of the three number 21's in two of the Down syndrome offspring were of maternal origin. Five cytogenetic surveys in which both parents of a child with trisomy 21 were studied have been reviewed. From these data, it is estimated that 3% of couples producing a child with trisomy 21 can be explained by parental mosaicism. From 17 informative sibships, with one parent mosaic, the segregation ratio was estimated to be 0.43 +/- 0.11.
对一个家庭进行了研究,该家庭有三个患21三体综合征的孩子,母亲表型正常,是21三体/正常嵌合体。利用21号染色体荧光多态性证明,两个唐氏综合征患儿的三条21号染色体中有两条来自母亲。回顾了五项细胞遗传学调查,这些调查研究了21三体综合征患儿的父母双方。根据这些数据估计,生出21三体综合征患儿的夫妇中,有3%可归因于父母嵌合体。在17个有信息价值的同胞关系中,父母一方为嵌合体,其分离比估计为0.43±0.11。