South ST - 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: south st. 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

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. Among authors: south st. 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.

3

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.

4

Unknown partner for USP6 and unusual SS18 rearrangement detected by fluorescence in situ hybridization in a solid aneurysmal bone cyst.

Geiersbach K, Rector LS, Sederberg M, Hooker A, Randall RL, Schiffman JD, South ST. Geiersbach K, et al. Among authors: south st. Cancer Genet. 2011 Apr;204(4):195-202. doi: 10.1016/j.cancergen.2011.01.004. Cancer Genet. 2011. PMID: 21536237

5

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: south st. 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

6

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: south st. 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

7

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

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

8

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: south st. Mol Cytogenet. 2015 Aug 7;8:60. doi: 10.1186/s13039-015-0156-1. eCollection 2015. Mol Cytogenet. 2015. PMID: 26257825 Free PMC article.

9

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: south st. 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

10

DNA copy number analysis of Grade II-III and Grade IV gliomas reveals differences in molecular ontogeny including chromothripsis associated with IDH mutation status.

Cohen A, Sato M, Aldape K, Mason CC, Alfaro-Munoz K, Heathcock L, South ST, Abegglen LM, Schiffman JD, Colman H. Cohen A, et al. Among authors: south st. Acta Neuropathol Commun. 2015 Jun 20;3:34. doi: 10.1186/s40478-015-0213-3. Acta Neuropathol Commun. 2015. PMID: 26091668 Free PMC article.

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