Genovese MJ - Search Results

1

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

2

Dialyzed fetal bovine serum increases cytogenetic fragile X expression.

Jenkins EC, Duncan CJ, Gu H, Genovese M, Krawczun MS. Jenkins EC, et al. 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

3

Progress toward an internal control system for fragile-X induction by 5-fluorodeoxyuridine in whole-blood cultures.

Jenkins EC, Duncan CJ, Sanz MM, Genovese M, Gu H, Schwartz-Richstein C, Lele KP, Salandi ML, Krawczun MS. Jenkins EC, et al. Pathobiology. 1990;58(4):236-40. doi: 10.1159/000163591. Pathobiology. 1990. PMID: 2147548

4

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. Am J Med Genet. 1994 Jul 15;51(4):436-42. doi: 10.1002/ajmg.1320510426. Am J Med Genet. 1994. PMID: 7943013

5

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. 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

6

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. Am J Med Genet. 1999 Apr 2;83(4):331-3. Am J Med Genet. 1999. PMID: 10208174

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. 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. 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

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. 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.

10

The feasibility of PCR-based diagnosis of Prader-Willi and Angelman syndromes using restriction analysis after bisulfite modification of genomic DNA.

Velinov M, Gu H, Genovese M, Duncan C, Brown WT, Jenkins E. Velinov M, et al. Mol Genet Metab. 2000 Jan;69(1):81-3. doi: 10.1006/mgme.1999.2941. Mol Genet Metab. 2000. PMID: 10655162

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