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Results: 1-6 |
Results: 6

Authors: Athan, ES Williamson, J Ciappa, A Santana, V Romas, SN Lee, JH Rondon, H Lantigua, RA Medrano, M Torres, M Arawaka, S Rogaeva, E Song, YQ Sato, C Kawarai, T Fafel, KC Boss, MA Seltzer, WK Stern, Y St George-Hyslop, P Tycko, B Mayeux, R
Citation: Es. Athan et al., A founder mutation in presenilin 1 causing early-onset Alzheimer disease in unrelated Caribbean Hispanic families, J AM MED A, 286(18), 2001, pp. 2257-2263

Authors: Kazazian, HA Boehm, CD Seltzer, WK
Citation: Ha. Kazazian et al., ACMG recommendations for standards for interpretation of sequence variations, GENET MED, 2(5), 2000, pp. 302-303

Authors: Sekul, E Carroll, JE Yaghmai, F Armstrong, DL Seltzer, WK
Citation: E. Sekul et al., Fatal infantile X-linked neuropathy, J CHILD NEU, 15(12), 2000, pp. 829-830

Authors: Felice, KJ Seltzer, WK
Citation: Kj. Felice et Wk. Seltzer, Severe X-linked Charcot-Marie-Tooth neuropathy due to new mutations [G59R(G -> C), W44X(G -> A)] in the connexin 32 gene, EUR NEUROL, 44(1), 2000, pp. 61-63

Authors: Spector, EB Seltzer, WK Goodman, SI
Citation: Eb. Spector et al., Assignment of electron transfer flavoprotein-ubiquinone oxidoreductase (ETF-QO) to human chromosome 4q33 by fluorescence in situ hybridization and somatic cell hybridization, MOL GEN MET, 67(4), 1999, pp. 364-367

Authors: Holmes, SE O'Hearn, EE McInnis, MG Gorelick-Feldman, DA Kleiderlein, JJ Callahan, C Kwak, NG Ingersoll-Ashworth, RG Sherr, M Sumner, AJ Sharp, AH Ananth, U Seltzer, WK Boss, MA Vieria-Saecker, AM Epplen, JT Riess, O Ross, CA Margolis, RL
Citation: Se. Holmes et al., Expansion of a novel CAG trinucleotide repeat in the 5 ' region of PPP2R2Bis associated with SCA12, NAT GENET, 23(4), 1999, pp. 391-392
Risultati: 1-6 |