Rowe LR - Search Results

1

Differentiation of malignant melanoma from benign nevus using a novel genomic microarray with low specimen requirements.

Chandler WM, Rowe LR, Florell SR, Jahromi MS, Schiffman JD, South ST. Chandler WM, et al. Among authors: rowe lr. Arch Pathol Lab Med. 2012 Aug;136(8):947-55. doi: 10.5858/arpa.2011-0330-OA. Arch Pathol Lab Med. 2012. PMID: 22849744 Free article.

2

Large clinically consequential imbalances detected at the breakpoints of apparently balanced and inherited chromosome rearrangements.

South ST, Rector L, Aston E, Rowe L, Yang SP. South ST, et al. J Mol Diagn. 2010 Sep;12(5):725-9. doi: 10.2353/jmoldx.2010.090234. Epub 2010 Jul 1. J Mol Diagn. 2010. PMID: 20595628 Free PMC article.

3

Chromosomal loss of 3q26.3-3q26.32, involving a partial neuroligin 1 deletion, identified by genomic microarray in a child with microcephaly, seizure disorder, and severe intellectual disability.

Millson A, Lagrave D, Willis MJ, Rowe LR, Lyon E, South ST. Millson A, et al. Among authors: rowe lr. Am J Med Genet A. 2012 Jan;158A(1):159-65. doi: 10.1002/ajmg.a.34349. Epub 2011 Nov 21. Am J Med Genet A. 2012. PMID: 22106001

4

Molecular inversion probe array for the genetic evaluation of stillbirth using formalin-fixed, paraffin-embedded tissue.

Rowe LR, Thaker HM, Opitz JM, Schiffman JD, Haddadin ZM, Erickson LK, South ST. Rowe LR, et al. J Mol Diagn. 2013 Jul;15(4):466-72. doi: 10.1016/j.jmoldx.2013.03.006. Epub 2013 May 10. J Mol Diagn. 2013. PMID: 23665195 Free article.

5

Two cases of Scimitar syndrome associated with multiple congenital skeletal anomalies and lacking abnormalities by genomic microarray analysis.

Lloyd IE, Rowe LR, Erickson LK, Paxton CN, South ST, Alashari M. Lloyd IE, et al. Among authors: rowe lr. Pediatr Dev Pathol. 2014 Sep-Oct;17(5):360-5. doi: 10.2350/14-04-1474-CR.1. Epub 2014 Jun 19. Pediatr Dev Pathol. 2014. PMID: 24945981

6

Streamlining the OncoScan® Array Procedure for Use in a Clinical Laboratory.

Paxton CN, Rowe LR, South ST. Paxton CN, et al. Among authors: rowe lr. J Assoc Genet Technol. 2015;41(2):61-5. J Assoc Genet Technol. 2015. PMID: 26214323

7

Observations of the genomic landscape beyond 1p19q deletions and EGFR amplification in glioma.

Paxton CN, Rowe LR, South ST. Paxton CN, et al. Among authors: rowe lr. Mol Cytogenet. 2015 Aug 7;8:60. doi: 10.1186/s13039-015-0156-1. eCollection 2015. Mol Cytogenet. 2015. PMID: 26257825 Free PMC article.

8

Braddock-Carey syndrome: A 21q22 contiguous gene syndrome encompassing RUNX1.

Braddock SR, South ST, Schiffman JD, Longhurst M, Rowe LR, Carey JC. Braddock SR, et al. Among authors: rowe lr. Am J Med Genet A. 2016 Oct;170(10):2580-6. doi: 10.1002/ajmg.a.37870. Epub 2016 Aug 23. Am J Med Genet A. 2016. PMID: 27549381

9

Detection of BRAF V600E activating mutation in papillary thyroid carcinoma using PCR with allele-specific fluorescent probe melting curve analysis.

Rowe LR, Bentz BG, Bentz JS. Rowe LR, et al. J Clin Pathol. 2007 Nov;60(11):1211-5. doi: 10.1136/jcp.2006.040105. Epub 2007 Feb 13. J Clin Pathol. 2007. PMID: 17298986 Free PMC article. Review.

10

U-type exchange is the most frequent mechanism for inverted duplication with terminal deletion rearrangements.

Rowe LR, Lee JY, Rector L, Kaminsky EB, Brothman AR, Martin CL, South ST. Rowe LR, et al. J Med Genet. 2009 Oct;46(10):694-702. doi: 10.1136/jmg.2008.065052. Epub 2009 Mar 16. J Med Genet. 2009. PMID: 19293169

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