Lin MS - Search Results

1

The sequence of DNA replication in an iso-dicentric X-chromosome in peripheral blood lymphocytes and skin fibroblasts from the same individual.

Lin MS, Wilson MG. Lin MS, et al. Hum Genet. 1983;65(2):139-43. doi: 10.1007/BF00286650. Hum Genet. 1983. PMID: 6654328

2

Comparison of expression of the fragile site at Xq27 in T and B lymphocytes.

Marchese CA, Lin MS, Wilson MG. Marchese CA, et al. Among authors: lin ms. Hum Genet. 1984;67(2):213. doi: 10.1007/BF00273003. Hum Genet. 1984. PMID: 6611290

3

Sister chromatid exchanges and chromosome aberrations in fibroblasts from patients with retinoblastoma.

Takabayashi T, Lin MS, Wilson MG. Takabayashi T, et al. Among authors: lin ms. Hum Genet. 1983;63(4):317-9. doi: 10.1007/BF00274753. Hum Genet. 1983. PMID: 6862435

4

DA/DAPI-fluorescent heteromorphism of human Y chromosome.

Lin MS, Zhang A, Wilson MG, Fujimoto A. Lin MS, et al. Hum Genet. 1988 May;79(1):36-8. doi: 10.1007/BF00291706. Hum Genet. 1988. PMID: 3366461

5

Expression of fragile X in human-mouse somatic cell hybrids.

Lin MS, Shimanuki K, Wilson MG. Lin MS, et al. Cytogenet Cell Genet. 1987;44(2-3):118-22. doi: 10.1159/000132355. Cytogenet Cell Genet. 1987. PMID: 3568760

6

Effect of C-banded heterochromatin on centromere separation.

Zhang A, Lin MS, Wilson MG. Zhang A, et al. Among authors: lin ms. Hum Hered. 1987;37(5):285-9. doi: 10.1159/000153719. Hum Hered. 1987. PMID: 3666759

7

Reduction of fragile X expression in blood after cryopreservation.

Shimanuki K, Lin MS, Wilson MG. Shimanuki K, et al. Among authors: lin ms. Am J Med Genet. 1985 Aug;21(4):771-5. doi: 10.1002/ajmg.1320210421. Am J Med Genet. 1985. PMID: 4025403

8

Ullrich-Turner syndrome associated with interstitial deletion of Xp11.4 leads to p22.31.

Wilson MG, Modebe O, Towner JW, Frasier SD, Lin MS. Wilson MG, et al. Among authors: lin ms. Am J Med Genet. 1983 Mar;14(3):567-76. doi: 10.1002/ajmg.1320140321. Am J Med Genet. 1983. PMID: 6859107

9

Sister chromatid exchanges in the human active and inactive X chromosomes.

Zhang A, Lin MS, Wilson MG, Fujimoto A. Zhang A, et al. Among authors: lin ms. Cytogenet Cell Genet. 1989;52(1-2):79-82. doi: 10.1159/000132845. Cytogenet Cell Genet. 1989. PMID: 2612219

10

The prenatal detection of the fragile X chromosome: review of recent experience.

Jenkins EC, Brown WT, Wilson MG, Lin MS, Alfi OS, Wassman ER, Brooks J, Duncan CJ, Masia A, Krawczun MS. Jenkins EC, et al. Among authors: lin ms. Am J Med Genet. 1986 Jan-Feb;23(1-2):297-311. doi: 10.1002/ajmg.1320230123. Am J Med Genet. 1986. PMID: 2937295 Review.

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