Lin MS - Search Results

1

Chromosome mosaicism in 6,000 amniocenteses.

Wilson MG, Lin MS, Fujimoto A, Herbert W, Kaplan FM. Wilson MG, et al. Among authors: lin ms. Am J Med Genet. 1989 Apr;32(4):506-13. doi: 10.1002/ajmg.1320320417. Am J Med Genet. 1989. PMID: 2773995

2

Prenatal diagnosis of mosaicism for del(18)(q12.2q21.1) and a normal cell line.

Wilson MG, Lin MS. Wilson MG, et al. Among authors: lin ms. J Med Genet. 1988 Sep;25(9):635-6. doi: 10.1136/jmg.25.9.635. J Med Genet. 1988. PMID: 3184145 Free PMC article. No abstract available.

3

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

4

Trisomy 14 mosaicism with t(14;15)(q11;p11) in offspring of a balanced translocation carrier mother.

Fujimoto A, Lin MS, Korula SR, Wilson MG. Fujimoto A, et al. Among authors: lin ms. Am J Med Genet. 1985 Oct;22(2):333-42. doi: 10.1002/ajmg.1320220217. Am J Med Genet. 1985. PMID: 4050866

5

Asynchronous DNA replication between 15q11.2q12 homologs: cytogenetic evidence for maternal imprinting and delayed replication.

Lin MS, Zhang A, Fujimoto A. Lin MS, et al. Hum Genet. 1995 Nov;96(5):572-6. doi: 10.1007/BF00197413. Hum Genet. 1995. PMID: 8530005

6

Direct duplication of 9p22-->p24 in a child with duplication 9p syndrome.

Fujimoto A, Lin MS, Schwartz S. Fujimoto A, et al. Among authors: lin ms. Am J Med Genet. 1998 May 26;77(4):268-71. Am J Med Genet. 1998. PMID: 9600733

7

Monozygotic twins of discordant sex both with 45,X/46,X,idic(Y) mosaicism.

Fujimoto A, Boelter WD, Sparkes RS, Lin MS, Battersby K. Fujimoto A, et al. Among authors: lin ms. Am J Med Genet. 1991 Nov 1;41(2):239-45. doi: 10.1002/ajmg.1320410222. Am J Med Genet. 1991. PMID: 1785642 Review.

8

Lack of specificity of DA/DAPI fluorescence.

Lin MS, Huynh KH, Fujimoto A, Wilson MG. Lin MS, et al. Clin Genet. 1990 Jan;37(1):74-7. doi: 10.1111/j.1399-0004.1990.tb03394.x. Clin Genet. 1990. PMID: 2302826

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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