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Rare trisomy mosaicism diagnosed in amniocytes, involving an autosome other than chromosomes 13, 18, 20, and 21: karyotype/phenotype correlations.
Hsu LY, Yu MT, Neu RL, Van Dyke DL, Benn PA, Bradshaw CL, Shaffer LG, Higgins RR, Khodr GS, Morton CC, Wang H, Brothman AR, Chadwick D, Disteche CM, Jenkins LS, Kalousek DK, Pantzar TJ, Wyatt P. Hsu LY, et al. Among authors: shaffer lg. Prenat Diagn. 1997 Mar;17(3):201-42. doi: 10.1002/(sici)1097-0223(199703)17:3<201::aid-pd56>3.0.co;2-h. Prenat Diagn. 1997. PMID: 9110367
Common trisomy mosaicism diagnosed in amniocytes involving chromosomes 13, 18, 20 and 21: karyotype-phenotype correlations.
Wallerstein R, Yu MT, Neu RL, Benn P, Lee Bowen C, Crandall B, Disteche C, Donahue R, Harrison B, Hershey D, Higgins RR, Jenkins LS, Jackson-Cook C, Keitges E, Khodr G, Lin CC, Luthardt FW, Meisner L, Mengden G, Patil SR, Rodriguez M, Sciorra LJ, Shaffer LG, Stetten G, Van Dyke DL, Wang H. Wallerstein R, et al. Among authors: shaffer lg. Prenat Diagn. 2000 Feb;20(2):103-22. Prenat Diagn. 2000. PMID: 10694683
Mosaicism for trisomy 12: four cases with varying outcomes.
Bischoff FZ, Zenger-Hain J, Moses D, Van Dyke DL, Shaffer LG. Bischoff FZ, et al. Among authors: shaffer lg. Prenat Diagn. 1995 Nov;15(11):1017-26. doi: 10.1002/pd.1970151106. Prenat Diagn. 1995. PMID: 8606880
Molecular characterization of de novo secondary trisomy 13.
Shaffer LG, McCaskill C, Han JY, Choo KH, Cutillo DM, Donnenfeld AE, Weiss L, Van Dyke DL. Shaffer LG, et al. Am J Hum Genet. 1994 Nov;55(5):968-74. Am J Hum Genet. 1994. PMID: 7977360 Free PMC article.
354 results