Wilson MG - Search Results

1

Chromosome mosaicism in 6,000 amniocenteses.

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

2

Lack of specificity of DA/DAPI fluorescence.

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

3

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: wilson mg. Cytogenet Cell Genet. 1989;52(1-2):79-82. doi: 10.1159/000132845. Cytogenet Cell Genet. 1989. PMID: 2612219

4

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

Wilson MG, Lin MS. Wilson MG, et al. 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.

5

DA/DAPI-fluorescent heteromorphism of human Y chromosome.

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

6

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: wilson mg. Am J Med Genet. 1985 Oct;22(2):333-42. doi: 10.1002/ajmg.1320220217. Am J Med Genet. 1985. PMID: 4050866

7

Double autosomal trisomy and mosaicism for chromosomes no. 8 and no. 21.

Wilson MG, Fujimoto A, Alfi OS. Wilson MG, et al. J Med Genet. 1974 Mar;11(1):96-101. doi: 10.1136/jmg.11.1.96. J Med Genet. 1974. PMID: 4134622 Free PMC article.

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. 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 and chromosome aberrations in fibroblasts from patients with retinoblastoma.

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

10

A rare 6q11+ heteromorphism: cytogenetic analysis and in situ hybridization.

Lin MS, Zhang A, Fujimoto A, Wilson MG. Lin MS, et al. Among authors: wilson mg. Hum Hered. 1994 Jan-Feb;44(1):31-6. doi: 10.1159/000154186. Hum Hered. 1994. PMID: 8163289

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