Genovese M - Search Results

1

Ultrastructure of the fragile X chromosome: new observations on the fragile site.

Wen GY, Jenkins EC, Goldberg EM, Genovese M, Brown WT, Wisniewski HM. Wen GY, et al. Among authors: genovese m. Am J Med Genet. 1999 Apr 2;83(4):331-3. Am J Med Genet. 1999. PMID: 10208174

2

Human chromatid ultrastructure: new observations with scanning and transmission electron microscopy.

Jenkins EC, Wen GY, Jenkins EC Jr, Genovese M, Brown WT. Jenkins EC, et al. Among authors: genovese m. Scanning. 2002 Mar-Apr;24(2):55-8. doi: 10.1002/sca.4950240201. Scanning. 2002. PMID: 12004804

3

Brush-like fibers on the human chromosome periphery.

Wen GY, Fisher MB, Genovese M, Goldberg EM, Jenkins EC. Wen GY, et al. Among authors: genovese m. Scanning. 2003 Nov-Dec;25(6):316-20. doi: 10.1002/sca.4950250608. Scanning. 2003. PMID: 14696981

4

Fra(X)(q27.2), the common fragile site, observed in only one of 760 cases studied for the fragile X syndrome.

Jenkins EC, Genovese MJ, Duncan CJ, Gu H, Stark-Houck SL, Lele K, Li SY, Krawczun MS. Jenkins EC, et al. Among authors: genovese mj. Am J Med Genet. 1992 Apr 15-May 1;43(1-2):136-41. doi: 10.1002/ajmg.1320430121. Am J Med Genet. 1992. PMID: 1605182

5

Dialyzed fetal bovine serum increases cytogenetic fragile X expression.

Jenkins EC, Duncan CJ, Gu H, Genovese M, Krawczun MS. Jenkins EC, et al. Among authors: genovese m. Am J Med Genet. 1992 Apr 15-May 1;43(1-2):155-60. doi: 10.1002/ajmg.1320430124. Am J Med Genet. 1992. PMID: 1534967

6

Fragile X induction systems in CVS cultures: effect on cytogenetic, PCR, and genomic Southern Blot DNA analyses of the FMR-1 gene.

Jenkins EC, Morys I, Henderson J, Genovese M, Carter M, Li SY, Houck GE Jr, Ding X, Stark-Houck SL, Dobkin CS, et al. Jenkins EC, et al. Among authors: genovese m. Am J Med Genet. 1994 Jul 15;51(4):436-42. doi: 10.1002/ajmg.1320510426. Am J Med Genet. 1994. PMID: 7943013

7

Occurrence of aneuploidy for the X chromosome in over 1,300 unrelated specimens screened for the fragile X chromosome.

Jenkins EC, Genovese M, Duncan CJ, Gu H, Stark-Houck S, Li SY, Henderson J, Morys I, Brown WT. Jenkins EC, et al. Among authors: genovese m. Am J Med Genet. 1994 Jul 15;51(4):452-3. doi: 10.1002/ajmg.1320510430. Am J Med Genet. 1994. PMID: 7943017 No abstract available.

8

Increased low-level chromosome 21 mosaicism in older individuals with Down syndrome.

Jenkins EC, Schupf N, Genovese M, Ye LL, Kapell D, Canto B, Harris M, Devenny D, Lee JH, Brown WT. Jenkins EC, et al. Among authors: genovese m. Am J Med Genet. 1997 Jan 20;68(2):147-51. doi: 10.1002/(sici)1096-8628(19970120)68:2<147::aid-ajmg5>3.0.co;2-m. Am J Med Genet. 1997. PMID: 9028448

9

Normal adaptive function with learning disability in duplication 8p including band p22.

Sklower Brooks SS, Genovese M, Gu H, Duncan CJ, Shanske A, Jenkins EC. Sklower Brooks SS, et al. Among authors: genovese m. Am J Med Genet. 1998 Jun 30;78(2):114-7. doi: 10.1002/(sici)1096-8628(19980630)78:2<114::aid-ajmg3>3.3.co;2-6. Am J Med Genet. 1998. PMID: 9674899

10

First transmission electron micrograph of continuous mitotic spindle fibers between polar area and chromosome ends.

Wen GY, Jenkins EC, Goldberg EM, Genovese M, Brown WT, Wisniewski HM. Wen GY, et al. Among authors: genovese m. Am J Med Genet. 1999 Apr 2;83(4):334-7. doi: 10.1002/(sici)1096-8628(19990402)83:4<334::aid-ajmg22>3.0.co;2-i. Am J Med Genet. 1999. PMID: 10208175 No abstract available.

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