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Results: 1-5 |
Results: 5

Authors: Beaty, TH Wang, H Hetmanski, JB Fan, YT Zeiger, JS Liang, KY Chiu, YF Vanderkolk, CA Seifert, KC Wulfsberg, EA Raymond, G Panny, SR McIntosh, I
Citation: Th. Beaty et al., A case-control study of nonsyndromic oral clefts in Maryland, ANN EPIDEMI, 11(6), 2001, pp. 434-442

Authors: Norris, RA Scott, KK Moore, CS Stetten, G Brown, CR Jabs, EW Wulfsberg, EA Yu, J Kern, MJ
Citation: Ra. Norris et al., Human PRRX1 and PRRX2 genes: cloning, expression, genomic localization, and exclusion as disease genes for Nager syndrome, MAMM GENOME, 11(11), 2000, pp. 1000-1005

Authors: Olander, E Stamberg, J Steinberg, L Wulfsberg, EA
Citation: E. Olander et al., Third Prader-Willi syndrome phenotype due to maternal uniparental disomy 15 with mosaic trisomy 15, AM J MED G, 93(3), 2000, pp. 215-218

Authors: Wulfsberg, EA
Citation: Ea. Wulfsberg, The impact of genetic testing on primary care: Where's the beef?, AM FAM PHYS, 61(4), 2000, pp. 971

Authors: Lee, DH Cottrell, JR Sanders, RC Meyers, CM Wulfsberg, EA Sun, CCJ
Citation: Dh. Lee et al., OEIS complex (omphalocele exstrophy imperforate anus spinal defects) in monozygotic twins, AM J MED G, 84(1), 1999, pp. 29-33
Risultati: 1-5 |