Cotter PD - Search Results

1

Detection of single clone deletions using array CGH: identification of submicroscopic deletions in the 22q11.2 deletion syndrome as a model system.

Tokuyasu TA, Cotter PD, Segraves R, Harris J, Elder ME, Gonzales M, Pinkel D, Albertson DG, Rauen KA. Tokuyasu TA, et al. Among authors: cotter pd. Am J Med Genet A. 2007 May 1;143A(9):925-32. doi: 10.1002/ajmg.a.31662. Am J Med Genet A. 2007. PMID: 17394204

2

Additional patient with del(12)(q21.2q22): further evidence for a candidate region for cardio-facio-cutaneous syndrome?

Rauen KA, Albertson DG, Pinkel D, Cotter PD. Rauen KA, et al. Among authors: cotter pd. Am J Med Genet. 2002 Jun 1;110(1):51-6. doi: 10.1002/ajmg.10478. Am J Med Genet. 2002. PMID: 12116271

3

Xq chromosome duplication in males: clinical, cytogenetic and array CGH characterization of a new case and review.

Cheng SF, Rauen KA, Pinkel D, Albertson DG, Cotter PD. Cheng SF, et al. Among authors: cotter pd. Am J Med Genet A. 2005 Jun 15;135(3):308-13. doi: 10.1002/ajmg.a.30613. Am J Med Genet A. 2005. PMID: 15887264 Review.

4

Interstitial deletion of chromosome 12q: genotype-phenotype correlation of two patients utilizing array comparative genomic hybridization.

Klein OD, Cotter PD, Schmidt AM, Bick DP, Tidyman WE, Albertson DG, Pinkel D, Rauen KA. Klein OD, et al. Among authors: cotter pd. Am J Med Genet A. 2005 Nov 1;138(4):349-54. doi: 10.1002/ajmg.a.30867. Am J Med Genet A. 2005. PMID: 16200635

5

Duplication of distal 20q: clinical, cytogenetic and array CGH. Characterization of a new case.

Iglesias A, Rauen KA, Albertson DG, Pinkel D, Cotter PD. Iglesias A, et al. Among authors: cotter pd. Clin Dysmorphol. 2006 Jan;15(1):19-23. doi: 10.1097/01.mcd.0000184969.84280.e1. Clin Dysmorphol. 2006. PMID: 16317302

6

Supernumerary marker chromosomes derived from chromosome 6: cytogenetic, molecular cytogenetic, and array CGH characterization.

Huang B, Pearle P, Rauen KA, Cotter PD. Huang B, et al. Among authors: cotter pd. Am J Med Genet A. 2012 Jul;158A(7):1568-73. doi: 10.1002/ajmg.a.35385. Epub 2012 May 25. Am J Med Genet A. 2012. PMID: 22639445 Free PMC article.

7

Cardio-facio-cutaneous syndrome phenotype in an individual with an interstitial deletion of 12q: identification of a candidate region for CFC syndrome.

Rauen KA, Cotter PD, Bitts SM, Cox VA, Golabi M. Rauen KA, et al. Among authors: cotter pd. Am J Med Genet. 2000 Jul 31;93(3):219-22. doi: 10.1002/1096-8628(20000731)93:3<219::aid-ajmg12>3.0.co;2-5. Am J Med Genet. 2000. PMID: 10925386

8

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

9

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

10

Cardio-facio-cutaneous syndrome phenotype and del(12q).

Rauen KA, Cotter PD. Rauen KA, et al. Among authors: cotter pd. Am J Med Genet A. 2003 Feb 1;116A(4):411-2. doi: 10.1002/ajmg.a.10013. Am J Med Genet A. 2003. PMID: 12522803 No abstract available.

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