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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: brothman ar. 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
Genomic medicine in prenatal diagnosis.
South ST, Chen Z, Brothman AR. South ST, et al. Among authors: brothman ar. Clin Obstet Gynecol. 2008 Mar;51(1):62-73. doi: 10.1097/GRF.0b013e3181616509. Clin Obstet Gynecol. 2008. PMID: 18303500 Review.
129 results