Duncan CJ - Search Results

1

Chromosomal abnormalities in amniotic fluid cell cultures: a comparison of apparent pseudomosaicism in Chang and RPMI-1640 media.

Krawczun MS, Jenkins EC, Masia A, Kunaporn S, Stark SL, Duncan CJ, Sklower SL, Rudelli RD. Krawczun MS, et al. Among authors: duncan cj. Clin Genet. 1989 Feb;35(2):139-45. doi: 10.1111/j.1399-0004.1989.tb02919.x. Clin Genet. 1989. PMID: 2721022

2

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: duncan cj. 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

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: duncan cj. 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

4

Fra(X) prenatal diagnosis: are endoreduplicated and polyploid cells useful diagnostic criteria?

Krawczun MS, Duncan CJ, Stark-Houck SL, Jenkins EC. Krawczun MS, et al. Among authors: duncan cj. Am J Med Genet. 1992 Apr 15-May 1;43(1-2):149-54. doi: 10.1002/ajmg.1320430123. Am J Med Genet. 1992. PMID: 1605184

5

Improved prenatal detection of fra(X)(q27.3): methods for prevention of false negatives in chorionic villus and amniotic fluid cell cultures.

Jenkins EC, Krawczun MS, Stark-Houck SL, Duncan CJ, Kunaporn S, Gu H, Schwartz-Richstein C, Howard-Peebles PN, Gross A, Sherman SL, et al. Jenkins EC, et al. Among authors: duncan cj. Am J Med Genet. 1991 Feb-Mar;38(2-3):447-52. doi: 10.1002/ajmg.1320380262. Am J Med Genet. 1991. PMID: 1826813

6

SV40-transformed fragile (X) amniocytes.

Jenkins EC, Brooks SE, Stark-Houck SL, Duncan CJ, Brooks SL, Brown WT. Jenkins EC, et al. Among authors: duncan cj. Am J Med Genet. 1991 Feb-Mar;38(2-3):464-6. doi: 10.1002/ajmg.1320380265. Am J Med Genet. 1991. PMID: 1850194

7

Distribution of autosomal fragile sites in specimens cultured for prenatal fragile X diagnosis.

Krawczun MS, Jenkins EC, Duncan CJ, Stark-Houck SL, Kunaporn S, Schwatz-Richstein C, Gu H, Brown WT. Krawczun MS, et al. Among authors: duncan cj. Am J Med Genet. 1991 Feb-Mar;38(2-3):456-63. doi: 10.1002/ajmg.1320380264. Am J Med Genet. 1991. PMID: 2018087

8

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. Among authors: duncan cj. Pathobiology. 1990;58(4):236-40. doi: 10.1159/000163591. Pathobiology. 1990. PMID: 2147548

9

Further evidence for genetic heterogeneity in the fragile X syndrome.

Brown WT, Jenkins EC, Gross AC, Chan CB, Krawczun MS, Duncan CJ, Sklower SL, Fisch GS. Brown WT, et al. Among authors: duncan cj. Hum Genet. 1987 Apr;75(4):311-21. doi: 10.1007/BF00284100. Hum Genet. 1987. PMID: 2883105

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: duncan cj. 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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