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Vallente RU, Cheng EY, Hassold TJ. The synaptonemal complex and meiotic recombination in humans: new approaches to old questions (Review). Chromosoma 2006;115:241-249.
Cheng EY, Goss CH, McKone EF, Galic V, Debleq CK, Tonelli MR, Aitken ML. Aggressive prenatal care results in successful fetal outcomes in CF women. J Cystic Fibrosis 2006;5:85-91.
Bennett R, Motulsky A, Bittles A, Hudgins L, Uhrich S, Locher-Doyle D, Sylvie K, Scott CR, Cheng E, McGilvray B, Steiner R, Olson D. Genetic counseling and screening of consanguineous couples and their offspring: Recommendations of the National Society of Genetic Counselors. J Genet Counseling 2002;11(2):97-119.
Cubert R, Cheng EY, Mack S, Pepin MG, Byers PH. Osteogenesis imperfecta: Mode of delivery and neonatal outcome. Obstet Gynecol 2001;97:66–69.
Cheng EY, Chen YJ, Disteche CM, Gartler SM. Analysis of a paracentric
inversion in human oocytes: non-homologous pairing in pachytene. Hum Genet
1999;105:191–196.
Cheng EY, Chen YJ, Bonnet G, Gartler SM. An analysis of meiotic pairing in trisomy 21 oocytes using fluorescent in situ hybridization. Cytogenetics and Cell Genetics 1998;80:48–53.
Cheng EY, Chen YJ, Gartler SM. Chromosome painting analysis of early oogenesis in trisomy 18. Cytogenetics and Cell Genetics 1995;70:205–210.
Cheng EY and Gartler SM. A fluorescent in situ hybridization analysis of X chromosome pairing in human female meiosis. Hum Genet 1994; 94:389–94.
Cheng EY, Luthy DA, Zebelman AM, Williams MA, Luthardt FW, Hickok DE, Lieppman RE, Coe SJ. A midtrimester screening test for fetal Down syndrome utilizing maternal serum alpha-fetoprotein, human chorionic gonadotropin, and unconjugated estriol. Obstet Gynecol 1993;81:72–77.
Ashwood ER, Cheng EY, Luthy DA. Maternal serum alpha-fetoprotein and fetal trisomy-21 in women 35 years and older: Implications for alpha-fetoprotein screening programs. Am J Med Genet 1987;26(3):531–539.
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