1. Review and hypothesis: somatic mosaicism: observations related to clinical genetics;Hall, J.G.;Am J Hum Genet,1988
2. Duchenne muscular dystrophy (DMD)/Becker muscular dystrophy (BMD) families studied with the dystrophin cDNA: location of breakpoints on Hind III and Bgl II exon-containing fragment maps, meiotic and mitotic origin of the mutations;Am J Hum Genet,1988
3. Germinal mosaicism in Duchenne muscular dystrophy;Wood, S.; McGillivray, B.C.;Hum Genet,1988
4. Three different, non-mosaic sex chromosome abnormalities (direct cytotrophoblasts, mesenchymal core cultures, and abortus skin fibroblasts): implications for elucidating chorionic villi mosaicism with DMD, and that subject I.2 had transmitted three types of gametes: (1) one bearing the deletion (II.3); (2) one non-deleted and non-recombined,(3)
5. metaphases analysed from cytotrophoblasts contained 44 autosomes, one normal X chromosome, and one abnormal, nearly acrocentric, chromosome (figure a), which appeared to be an inverted X chromosome. Each of Received for publication,1989