Cotter PD - Search Results

1

A multiplex methylation PCR assay for identification of uniparental disomy of chromosome 7.

Moore MW, Dietz LG, Tirtorahardjo B, Cotter PD. Moore MW, et al. Among authors: cotter pd. Hum Mutat. 2003 Jun;21(6):645-8. doi: 10.1002/humu.10222. Hum Mutat. 2003. PMID: 12754712

2

Acquired inv(9): what is its significance?

Betz JL, Behairy AS, Rabionet P, Tirtorahardjo B, Moore MW, Cotter PD. Betz JL, et al. Among authors: cotter pd. Cancer Genet Cytogenet. 2005 Jul 1;160(1):76-8. doi: 10.1016/j.cancergencyto.2004.12.002. Cancer Genet Cytogenet. 2005. PMID: 15949575

3

Prenatal diagnosis of supernumerary marker 15 chromosomes and exclusion of uniparental disomy for chromosome 15.

Cotter PD, Ledesma CT, Dietz LG, Pusso S, Wohlferd MM, Goldberg JD. Cotter PD, et al. Prenat Diagn. 1999 Aug;19(8):721-6. Prenat Diagn. 1999. PMID: 10451515 Review.

4

Exclusion of maternal uniparental disomy of chromosome 14 in patients referred for Prader-Willi syndrome using a multiplex methylation polymerase chain reaction assay.

Dietz LG, Wylie AA, Rauen KA, Murphy SK, Jirtle RL, Cotter PD. Dietz LG, et al. Among authors: cotter pd. J Med Genet. 2003 Apr;40(4):e46. doi: 10.1136/jmg.40.4.e46. J Med Genet. 2003. PMID: 12676919 Free PMC article. No abstract available.

5

Prader-Willi syndrome resulting from an unbalanced translocation: characterization by array comparative genomic hybridization.

Klein OD, Cotter PD, Albertson DG, Pinkel D, Tidyman WE, Moore MW, Rauen KA. Klein OD, et al. Among authors: cotter pd. Clin Genet. 2004 Jun;65(6):477-82. doi: 10.1111/j.0009-9163.2004.00261.x. Clin Genet. 2004. PMID: 15151506

6

Genomic Rearrangements of PTEN in Prostate Cancer.

Phin S, Moore MW, Cotter PD. Phin S, et al. Among authors: cotter pd. Front Oncol. 2013 Sep 17;3:240. doi: 10.3389/fonc.2013.00240. Front Oncol. 2013. PMID: 24062990 Free PMC article. Review.

7

Challenges in the codevelopment of companion diagnostics.

Moore MW, Babu D, Cotter PD. Moore MW, et al. Among authors: cotter pd. Per Med. 2012 Jul;9(5):485-496. doi: 10.2217/pme.12.60. Per Med. 2012. PMID: 29768776 Free article.

8

Reference Size Matching, Whole-Genome Amplification, and Fluorescent Labeling as a Method for Chromosomal Microarray Analysis of Clinically Actionable Copy Number Alterations in Formalin-Fixed, Paraffin-Embedded Tumor Tissue.

Gunn SR, Govender S, Sims CL, Khurana A, Koo S, Scoggin J, Moore MW, Cotter PD. Gunn SR, et al. Among authors: cotter pd. J Mol Diagn. 2018 May;20(3):279-288. doi: 10.1016/j.jmoldx.2018.01.004. Epub 2018 Feb 19. J Mol Diagn. 2018. PMID: 29471114 Free article.

9

Epigenetic detection of human chromosome 14 uniparental disomy.

Murphy SK, Wylie AA, Coveler KJ, Cotter PD, Papenhausen PR, Sutton VR, Shaffer LG, Jirtle RL. Murphy SK, et al. Among authors: cotter pd. Hum Mutat. 2003 Jul;22(1):92-7. doi: 10.1002/humu.10237. Hum Mutat. 2003. PMID: 12815599

10

Interstitial deletions of chromosome 6q: genotype-phenotype correlation utilizing array CGH.

Klein OD, Cotter PD, Moore MW, Zanko A, Gilats M, Epstein CJ, Conte F, Rauen KA. Klein OD, et al. Among authors: cotter pd. Clin Genet. 2007 Mar;71(3):260-6. doi: 10.1111/j.1399-0004.2007.00757.x. Clin Genet. 2007. PMID: 17309649

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