Jenkins E - Search Results

1

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. Among authors: jenkins e. Mol Genet Metab. 2000 Jan;69(1):81-3. doi: 10.1006/mgme.1999.2941. Mol Genet Metab. 2000. PMID: 10655162

2

Prenatal diagnosis and carrier screening for fragile X by PCR.

Brown WT, Nolin S, Houck G Jr, Ding X, Glicksman A, Li SY, Stark-Houck S, Brophy P, Duncan C, Dobkin C, Jenkins E. Brown WT, et al. Among authors: jenkins e. Am J Med Genet. 1996 Jul 12;64(1):191-5. doi: 10.1002/(SICI)1096-8628(19960712)64:1<191::AID-AJMG34>3.0.CO;2-G. Am J Med Genet. 1996. PMID: 8826474

3

PCR-based methylation testing for Prader-Willi or Angelman syndromes using archived fixed-cell suspensions.

Velinov M, Gu H, Shah K, Genovese M, Duncan C, Kupchik G, Jenkins EC. Velinov M, et al. Among authors: jenkins ec. Genet Test. 2001 Summer;5(2):153-5. doi: 10.1089/109065701753145655. Genet Test. 2001. PMID: 11551105

4

Recent experience in prenatal fra(X) detection.

Jenkins EC, Brown WT, Krawczun MS, Duncan CJ, Lele KP, Cantu ES, Schonberg S, Golbus MS, Sekhon GS, Stark S, et al. Jenkins EC, et al. Am J Med Genet. 1988 May-Jun;30(1-2):329-36. doi: 10.1002/ajmg.1320300133. Am J Med Genet. 1988. PMID: 2972205

5

Fragile X expression in short-term whole blood cultures is affected by cell density.

Krawczun MS, Jenkins EC, Brown WT, Silverman WP. Krawczun MS, et al. Among authors: jenkins ec. Am J Med Genet. 1988 May-Jun;30(1-2):435-42. doi: 10.1002/ajmg.1320300145. Am J Med Genet. 1988. PMID: 2972206

6

Constitutive fragile sites in fra(X) individuals.

Jenkins EC, Lele KP, Krawczun MS, Gross AC, Duncan CJ, Brown WT. Jenkins EC, et al. Am J Med Genet. 1988 May-Jun;30(1-2):429-34. doi: 10.1002/ajmg.1320300144. Am J Med Genet. 1988. PMID: 3052066

7

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

8

Transmission electron microscopy of chromosomes by longitudinal section preparation: application to fragile X chromosome analysis.

Wen GY, Jenkins EC, Yao XL, Yoon D, Brown WT, Wisniewski HM. Wen GY, et al. Among authors: jenkins ec. Am J Med Genet. 1997 Feb 11;68(4):445-9. doi: 10.1002/(sici)1096-8628(19970211)68:4<445::aid-ajmg14>3.0.co;2-s. Am J Med Genet. 1997. PMID: 9021019

9

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

10

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: jenkins ec. 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

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