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Results: 4

Authors: Storto, P Zackowski, J Leichtman, L Montgomery, T Newlin, A
Citation: P. Storto et al., Trisomy 1q42qter "syndrome": Additional case report, AM J MED G, 99(3), 2001, pp. 258-259

Authors: Booth, W Brodeur, P Buechner, F Ellsberg, P Fitch, NR Harris, MJ Harrison, J Herron, J Karlstrom, P Knighton, N Levine, P Meezan, W Miner, V Mitchell, JH Moore, KD Moore, RC Newlin, A Oates, JC Oneal, Z Provenzo, EF Roazen, P Sarah, R Segal, L Shields, D Siebers, T Small, D Song, C Spitz, EH Stavans, I Stilgoe, JR Trimble, S Warner, M West, P Wilson, EO
Citation: W. Booth et al., A Symposium on Secret Spaces of Childhood (Authors invited to contribute commentaries to help provide an iconography or conceptual map of the regionsof childhood), MICH Q REV, 39(3), 2000, pp. 439-530

Authors: McMahon, TT Shin, JA Newlin, A Edrington, TB Sugar, J Zadnik, K
Citation: Tt. Mcmahon et al., Discordance for keratoconus in two pairs of monozygotic twins, CORNEA, 18(4), 1999, pp. 444-451

Authors: Verghese, S Newlin, A Miller, M Burton, BK
Citation: S. Verghese et al., Mosaic trisomy 7 in a patient with pigmentary abnormalities, AM J MED G, 87(5), 1999, pp. 371-374
Risultati: 1-4 |