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Results: 1-4 |
Results: 4

Authors: Xiao, SX Yu, C Chou, XM Yuan, WJ Wang, Y Bu, L Fu, G Qian, MQ Yang, J Shi, YZ Hu, LD Han, B Wang, ZM Huang, W Liu, J Chen, Z Zhao, GP Kong, XY
Citation: Sx. Xiao et al., Dentinogenesis imperfecta 1 with or without progressive hearing loss is associated with distinct mutations in DSPP, NAT GENET, 27(2), 2001, pp. 201-204

Authors: Xiao, SX Bu, L Zhu, LQ Zheng, GY Yang, MH Qian, MQ Hu, LD Liu, J Zhao, GP Kong, XY
Citation: Sx. Xiao et al., A new locus for hereditary gingival fibromatosis (GINGF2) maps to 5q13-q22, GENOMICS, 74(2), 2001, pp. 180-185

Authors: Klempner, MS Schmid, CH Hu, LD Steere, AC Johnson, G McCloud, B Noring, R Weinstein, A
Citation: Ms. Klempner et al., Intralaboratory reliability of serologic and urine testing for Lyme disease, AM J MED, 110(3), 2001, pp. 217-219

Authors: Xiao, SX Wang, XR Qu, BY Yang, MH Liu, GY Bu, L Wang, Y Zhu, LQ Lei, H Hu, LD Zhang, XJ Liu, J Zhao, GP Kong, XY
Citation: Sx. Xiao et al., Refinement of the locus for autosomal dominant hereditary gingival fibromatosis (GINGF) to a 3.8-cM region on 2p21, GENOMICS, 68(3), 2000, pp. 247-252
Risultati: 1-4 |