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Results: 1-5 |
Results: 5

Authors: Davids, MS Crawford, E Weremowicz, S Morton, CC Copeland, NG Gilbert, DJ Jenkins, NA Phelan, MC Comb, MJ Melnick, MB
Citation: Ms. Davids et al., STK25 is a candidate gene for pseudopseudohypoparathyroidism, GENOMICS, 77(1-2), 2001, pp. 2-4

Authors: Phelan, MC Rogers, RC Michaelis, RC Moore, CL Blackburn, W
Citation: Mc. Phelan et al., Prenatal diagnosis of mosaicism for triploidy and trisomy 13, PRENAT DIAG, 21(6), 2001, pp. 457-460

Authors: Phelan, MC Rogers, RC Saul, RA Stapleton, GA Sweet, K McDermid, H Shaw, SR Claytor, J Willis, J Kelly, DP
Citation: Mc. Phelan et al., 22q13 deletion syndrome, AM J MED G, 101(2), 2001, pp. 91-99

Authors: Jarrett, KL Michaelis, RC Phelan, MC Vincent, VA Best, RG
Citation: Kl. Jarrett et al., Microsatellite analysis reveals a high incidence of maternal cell contamination in 46,XX products of conception consisting of villi or a combination of villi and membranous material, AM J OBST G, 185(1), 2001, pp. 198-203

Authors: Glenn, CC Deng, G Michaelis, RC Tarleton, J Phelan, MC Surh, L Yang, TP Driscoll, DJ
Citation: Cc. Glenn et al., DNA methylation analysis with respect to prenatal diagnosis of the Angelman and Prader-Willi syndromes and imprinting, PRENAT DIAG, 20(4), 2000, pp. 300-306
Risultati: 1-5 |