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Results: 1-5 |
Results: 5

Authors: Zhong, N Moroziewicz, DN Ju, WN Jurkiewicz, A Johnston, L Wisniewski, KE Brown, WT
Citation: N. Zhong et al., Heterogeneity of late-infantile neuronal ceroid lipofuscinosis, GENET MED, 2(6), 2000, pp. 312-318

Authors: Zhong, NA Wisniewski, KE Ju, WN Moroziewicz, DN Jurkiewicz, A McLendon, L Jenkins, EC Brown, WT
Citation: Na. Zhong et al., Molecular diagnosis of and carrier screening for the neuronal ceroid lipofuscinoses, GENET TEST, 4(3), 2000, pp. 243-248

Authors: Hartikainen, JM Ju, WN Wisniewski, KE Moroziewicz, DN Kaczmarski, AL McLendon, L Zhong, D Suarez, CT Brown, WT Zhong, N
Citation: Jm. Hartikainen et al., Late infantile neuronal ceroid lipofuscinosis is due to splicing mutationsin the CLN2 gene, MOL GEN MET, 67(2), 1999, pp. 162-168

Authors: Zhong, N Ju, WN Xu, WM Ye, LL Shen, Y Wu, GY Chen, SH Jin, RM Hu, XF Yang, AD Liu, XX Poon, P Pang, C Zheng, Y Song, L Zhao, P Fu, BJ Gu, HJ Brown, WT
Citation: N. Zhong et al., Frequency of the fragile X syndrome in Chinese mentally retarded populations is similar to that in Caucasians, AM J MED G, 84(3), 1999, pp. 191-194

Authors: Zhong, N Ju, WN Brown, WT Ye, LL Jenkins, EC Schupf, N
Citation: N. Zhong et al., Distribution of apolipoprotein E genotypes in fragile X syndrome and Batten disease, AM J MED G, 84(3), 1999, pp. 309-310
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