AAAAAA

   
Results: 1-8 |
Results: 8
Precursor B-cell lymphoblastic lymphoma - A study of nine cases lacking blood and bone marrow involvement and review of the literature
Authors: Maitra, A McKenna, RW Weinberg, AG Schneider, NR Kroft, SH
Citation: A. Maitra et al., Precursor B-cell lymphoblastic lymphoma - A study of nine cases lacking blood and bone marrow involvement and review of the literature, AM J CLIN P, 115(6), 2001, pp. 868-875
Secondary myelodysplasia with monosomy 7 arising after treatment for acutelymphoblastic leukemia in childhood
Authors: Aquino, VM Schneider, NR Sandler, ES
Citation: Vm. Aquino et al., Secondary myelodysplasia with monosomy 7 arising after treatment for acutelymphoblastic leukemia in childhood, J PED H ONC, 23(1), 2001, pp. 48-50
Mutations of the hSNF5/INI1 gene in renal rhabdoid tumors with second primary brain tumors
Authors: Savla, J Chen, TTY Schneider, NR Timmons, CF Delattre, O Tomlinson, GE
Citation: J. Savla et al., Mutations of the hSNF5/INI1 gene in renal rhabdoid tumors with second primary brain tumors, J NAT CANC, 92(8), 2000, pp. 648
Gas chromatography/mass spectrometry identification and quantification of isazophos in a famphur pour-on and in bovine tissues after a toxic exposure
Authors: Braselton, WE Johnson, JL Carlson, MP Schneider, NR
Citation: We. Braselton et al., Gas chromatography/mass spectrometry identification and quantification of isazophos in a famphur pour-on and in bovine tissues after a toxic exposure, J VET D INV, 12(1), 2000, pp. 15-20
New recurring cytogenetic abnormalities and association of blast cell karyotypes with prognosis in childhood T-cell acute lymphoblastic leukemia: a Pediatric Oncology Group report of 343 cases
Authors: Schneider, NR Carroll, AJ Shuster, JJ Pullen, DJ Link, MP Borowitz, MJ Camitta, BM Katz, JA Amylon, MD
Citation: Nr. Schneider et al., New recurring cytogenetic abnormalities and association of blast cell karyotypes with prognosis in childhood T-cell acute lymphoblastic leukemia: a Pediatric Oncology Group report of 343 cases, BLOOD, 96(7), 2000, pp. 2543-2549
Case report of a 22-week fetus with 47,XXX karyotype and multiple lower mesodermal defects
Authors: Hoang, MP Wilson, KS Schneider, NR Timmons, CF
Citation: Mp. Hoang et al., Case report of a 22-week fetus with 47,XXX karyotype and multiple lower mesodermal defects, PEDIATR D P, 2(1), 1999, pp. 58-61
Effects of supplementation of organic and inorganic of copper, cobalt, manganese, and zinc above requirement levels on postpartum two-year-old combinations nutrient cows
Authors: Olson, PA Brink, DR Hickok, DT Carlson, MP Schneider, NR Deutscher, GH Adams, DC Colburn, DJ Johnson, AB
Citation: Pa. Olson et al., Effects of supplementation of organic and inorganic of copper, cobalt, manganese, and zinc above requirement levels on postpartum two-year-old combinations nutrient cows, J ANIM SCI, 77(3), 1999, pp. 522-532
Extensive analysis of mosaicism in a case of Turner syndrome - The experience of 287 cytogenetic laboratories
Authors: Park, JP Brothman, AR Butler, MG Cooley, LD Dewald, GW Lundquist, KF Palmer, CG Patil, SR Rao, KW Saikevych, IA Schneider, NR Vance, GH
Citation: Jp. Park et al., Extensive analysis of mosaicism in a case of Turner syndrome - The experience of 287 cytogenetic laboratories, ARCH PATH L, 123(5), 1999, pp. 381-385
Risultati: 1-8 |