Jackson-Cook C - Search Results

1

Fluorescence in situ hybridization detectable mosaicism for Angelman syndrome with biparental methylation.

Tekin M, Jackson-Cook C, Buller A, Ferreira-Gonzalez A, Pandya A, Garrett CT, Bodurtha J. Tekin M, et al. Am J Med Genet. 2000 Nov 13;95(2):145-9. doi: 10.1002/1096-8628(20001113)95:2<145::aid-ajmg10>3.0.co;2-r. Am J Med Genet. 2000. PMID: 11078565

2

High BAALC expression associates with other molecular prognostic markers, poor outcome, and a distinct gene-expression signature in cytogenetically normal patients younger than 60 years with acute myeloid leukemia: a Cancer and Leukemia Group B (CALGB) study.

Langer C, Radmacher MD, Ruppert AS, Whitman SP, Paschka P, Mrózek K, Baldus CD, Vukosavljevic T, Liu CG, Ross ME, Powell BL, de la Chapelle A, Kolitz JE, Larson RA, Marcucci G, Bloomfield CD; Cancer and Leukemia Group B (CALGB). Langer C, et al. Blood. 2008 Jun 1;111(11):5371-9. doi: 10.1182/blood-2007-11-124958. Epub 2008 Mar 31. Blood. 2008. PMID: 18378853 Free PMC article. Clinical Trial.

3

New recurrent balanced translocations in acute myeloid leukemia and myelodysplastic syndromes: cancer and leukemia group B 8461.

Walker A, Mrózek K, Kohlschmidt J, Rao KW, Pettenati MJ, Sterling LJ, Marcucci G, Carroll AJ, Bloomfield CD; Alliance for Clinical Trials in Oncology. Walker A, et al. Genes Chromosomes Cancer. 2013 Apr;52(4):385-401. doi: 10.1002/gcc.22036. Epub 2012 Dec 10. Genes Chromosomes Cancer. 2013. PMID: 23225546 Free PMC article.

4

Parental origin determination in thirty de novo Robertsonian translocations.

Shaffer LG, Jackson-Cook CK, Stasiowski BA, Spence JE, Brown JA. Shaffer LG, et al. Am J Med Genet. 1992 Aug 1;43(6):957-63. doi: 10.1002/ajmg.1320430611. Am J Med Genet. 1992. PMID: 1357969

5

Three methods of fetal sampling in prenatal diagnosis.

Bodurtha J, Redwine F, Jackson-Cook C. Bodurtha J, et al. Va Med Q. 1992 Spring;119(2):93-5. Va Med Q. 1992. PMID: 1562622 Review. No abstract available.

6

Prenatal genetic counseling: what is fragile X?

Bodurtha J, Tams L, Jackson-Cook C. Bodurtha J, et al. Va Med Q. 1992 Spring;119(2):97-8. Va Med Q. 1992. PMID: 1562624 Review. No abstract available.

7

Partial trisomy 19p: case report and natural history.

Salbert BA, Solomon M, Spence JE, Jackson-Cook C, Brown J, Bodurtha J. Salbert BA, et al. Clin Genet. 1992 Mar;41(3):143-6. doi: 10.1111/j.1399-0004.1992.tb03651.x. Clin Genet. 1992. PMID: 1563088

8

Heritability and heteromorphic distributions of AluI chromosome banding variants in twins.

Huang B, Meyer JM, Jackson-Cook CK. Huang B, et al. Am J Med Genet. 1995 Jul 3;57(3):429-36. doi: 10.1002/ajmg.1320570313. Am J Med Genet. 1995. PMID: 7677146

9

Mental retardation and Ullrich-Turner syndrome in cases with 45,X/46X,+mar: additional support for the loss of the X-inactivation center hypothesis.

Cole H, Huang B, Salbert BA, Brown J, Howard-Peebles PN, Black SH, Dorfmann A, Febles OR, Stevens CA, Jackson-Cook C. Cole H, et al. Am J Med Genet. 1994 Aug 15;52(2):136-45. doi: 10.1002/ajmg.1320520204. Am J Med Genet. 1994. PMID: 7801998 Review.

10

46XY/47XYY mosaicism and fragile X.

Bodurtha J, Jackson-Cook C, Maddalena A, Piserchio J, Waller R. Bodurtha J, et al. Clin Genet. 1993 Aug;44(2):109-10. doi: 10.1111/j.1399-0004.1993.tb03858.x. Clin Genet. 1993. PMID: 8275558 No abstract available.

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