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Results: 1-3 |
Results: 3

Authors: Albers, S Marsden, D Quackenbush, E Stark, AR Levy, HL Irons, M
Citation: S. Albers et al., Detection of neonatal carnitine palmitoyltransferase II deficiency by expanded newborn screening with tandem mass spectrometry, PEDIATRICS, 107(6), 2001, pp. NIL_97-NIL_100

Authors: Khan, SG Levy, HL Legerski, R Quackenbush, E Reardon, JT Emmert, S Sancar, A Li, L Schneider, TD Cleaver, JE Kraemer, KH
Citation: Sg. Khan et al., Xeroderma pigmentosum group C splice mutation associated with autism and hypoglycinemia (vol 111, pg 791, 1998), J INVES DER, 112(3), 1999, pp. 402-402

Authors: Salgia, R Quackenbush, E Lin, J Souchkova, N Sattler, M Ewaniuk, DS Klucher, KM Daley, GQ Kraeft, SK Sackstein, R Alyea, EP von Andrian, UH Chen, LB Gutierrez-Ramos, JC Pendergast, AM Griffin, JD
Citation: R. Salgia et al., The BCR/ABL oncogene alters the chemotactic response to stromal-derived factor-1 alpha, BLOOD, 94(12), 1999, pp. 4233-4246
Risultati: 1-3 |