Brown WT - Search Results

1

FRAXAC1 and DXS548 polymorphisms in the Chinese population.

Poon PM, Pang CP, Chen QL, Zhong N, Lai KY, Lau CH, Wong CK, Brown WT. Poon PM, et al. Among authors: brown wt. Am J Med Genet. 1999 May 28;84(3):208-13. doi: 10.1002/(sici)1096-8628(19990528)84:3<208::aid-ajmg8>3.0.co;2-c. Am J Med Genet. 1999. PMID: 10331593

2

Trinucleotide CGG repeat in the FMR1 gene in Chinese mentally retarded patients.

Pang CP, Poon PM, Chen QL, Lai KY, Yin CH, Zhao Z, Zhong N, Lau CH, Lam ST, Wong CK, Brown WT. Pang CP, et al. Among authors: brown wt. Am J Med Genet. 1999 May 28;84(3):179-83. Am J Med Genet. 1999. PMID: 10331586

3

Frequency of the fragile X syndrome in Chinese mentally retarded populations is similar to that in Caucasians.

Zhong N, Ju W, Xu W, Ye L, Shen Y, Wu G, Chen SH, Jin R, Hu XF, Yang A, Liu X, Poon P, Pang C, Zheng Y, Song L, Zhao P, Fu B, Gu H, Brown WT. Zhong N, et al. Among authors: brown wt. Am J Med Genet. 1999 May 28;84(3):191-4. doi: 10.1002/(sici)1096-8628(19990528)84:3<191::aid-ajmg3>3.0.co;2-8. Am J Med Genet. 1999. PMID: 10331588

4

Fragile X gene instability: anchoring AGGs and linked microsatellites.

Zhong N, Yang W, Dobkin C, Brown WT. Zhong N, et al. Among authors: brown wt. Am J Hum Genet. 1995 Aug;57(2):351-61. Am J Hum Genet. 1995. PMID: 7668261 Free PMC article.

5

Fragile X founder chromosome effects: linkage disequilibrium or microsatellite heterogeneity?

Zhong N, Ye L, Dobkin C, Brown WT. Zhong N, et al. Among authors: brown wt. Am J Med Genet. 1994 Jul 15;51(4):405-11. doi: 10.1002/ajmg.1320510421. Am J Med Genet. 1994. PMID: 7943008

6

Distribution of FMR-1 and associated microsatellite alleles in a normal Chinese population.

Zhong N, Liu X, Gou S, Houck GE Jr, Li S, Dobkin C, Brown WT. Zhong N, et al. Among authors: brown wt. Am J Med Genet. 1994 Jul 15;51(4):417-22. doi: 10.1002/ajmg.1320510423. Am J Med Genet. 1994. PMID: 7943010

7

Positive fragile X microsatellite associations point to a common mechanism of dynamic mutation evolution.

Brown WT, Zhong N, Dobkin C. Brown WT, et al. Am J Hum Genet. 1996 Mar;58(3):641-3. Am J Hum Genet. 1996. PMID: 8644726 Free PMC article. No abstract available.

8

Fragile X founder effects and new mutations in Finland.

Zhong N, Kajanoja E, Smits B, Pietrofesa J, Curley D, Wang D, Ju W, Nolin S, Dobkin C, Ryynänen M, Brown WT. Zhong N, et al. Among authors: brown wt. Am J Med Genet. 1996 Jul 12;64(1):226-33. doi: 10.1002/(SICI)1096-8628(19960712)64:1<226::AID-AJMG41>3.0.CO;2-M. Am J Med Genet. 1996. PMID: 8826481

9

Fragile X "gray zone" alleles: AGG patterns, expansion risks, and associated haplotypes.

Zhong N, Ju W, Pietrofesa J, Wang D, Dobkin C, Brown WT. Zhong N, et al. Among authors: brown wt. Am J Med Genet. 1996 Aug 9;64(2):261-5. doi: 10.1002/(SICI)1096-8628(19960809)64:2<261::AID-AJMG5>3.0.CO;2-X. Am J Med Genet. 1996. PMID: 8844060

10

Reverse mutations in the fragile X syndrome.

Brown WT, Houck GE Jr, Ding X, Zhong N, Nolin S, Glicksman A, Dobkin C, Jenkins EC. Brown WT, et al. Am J Med Genet. 1996 Aug 9;64(2):287-92. doi: 10.1002/(SICI)1096-8628(19960809)64:2<287::AID-AJMG11>3.0.CO;2-B. Am J Med Genet. 1996. PMID: 8844067

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