Arrington CB - Search Results

1

Pathologic and molecular analysis in a family with rare mixed supravalvar aortic and pulmonic stenosis.

Arrington CB, Nightengale D, Lowichik A, Rosenthal ET, Christian-Ritter K, Viskochil DH. Arrington CB, et al. Pediatr Dev Pathol. 2006 Jul-Aug;9(4):297-306. doi: 10.2350/06-01-0014.1. Pediatr Dev Pathol. 2006. PMID: 16944981

2

Interstitial deletion 8q11.2-q13 with congenital anomalies of CHARGE association.

Arrington CB, Cowley BC, Nightingale DR, Zhou H, Brothman AR, Viskochil DH. Arrington CB, et al. Am J Med Genet A. 2005 Mar 15;133A(3):326-30. doi: 10.1002/ajmg.a.30562. Am J Med Genet A. 2005. PMID: 15672384

3

Exome analysis of a family with pleiotropic congenital heart disease.

Arrington CB, Bleyl SB, Matsunami N, Bonnell GD, Otterud BE, Nielsen DC, Stevens J, Levy S, Leppert MF, Bowles NE. Arrington CB, et al. Circ Cardiovasc Genet. 2012 Apr 1;5(2):175-82. doi: 10.1161/CIRCGENETICS.111.961797. Epub 2012 Feb 15. Circ Cardiovasc Genet. 2012. PMID: 22337856 Free PMC article.

4

Rapid progression of long-segment coarctation in a patient with Williams' syndrome.

Arrington C, Tristani-Firouzi M, Puchalski M. Arrington C, et al. Cardiol Young. 2005 Jun;15(3):312-4. doi: 10.1017/S104795110500065X. Cardiol Young. 2005. PMID: 15865838

5

Absence of TGFBR1 and TGFBR2 mutations in patients with bicuspid aortic valve and aortic dilation.

Arrington CB, Sower CT, Chuckwuk N, Stevens J, Leppert MF, Yetman AT, Bowles NE. Arrington CB, et al. Am J Cardiol. 2008 Sep 1;102(5):629-31. doi: 10.1016/j.amjcard.2008.04.044. Epub 2008 Jun 26. Am J Cardiol. 2008. PMID: 18721526

6

Family-based studies to identify genetic variants that cause congenital heart defects.

Arrington CB, Bleyl SB, Brunelli L, Bowles NE. Arrington CB, et al. Future Cardiol. 2013 Jul;9(4):507-18. doi: 10.2217/fca.13.40. Future Cardiol. 2013. PMID: 23834692 Review.

7

A family-based paradigm to identify candidate chromosomal regions for isolated congenital diaphragmatic hernia.

Arrington CB, Bleyl SB, Matsunami N, Bowles NE, Leppert TI, Demarest BL, Osborne K, Yoder BA, Byrne JL, Schiffman JD, Null DM, DiGeronimo R, Rollins M, Faix R, Comstock J, Camp NJ, Leppert MF, Yost HJ, Brunelli L. Arrington CB, et al. Am J Med Genet A. 2012 Dec;158A(12):3137-47. doi: 10.1002/ajmg.a.35664. Epub 2012 Nov 19. Am J Med Genet A. 2012. PMID: 23165927 Free PMC article.

8

Somatic mosaicism contributes to phenotypic variation in Timothy syndrome.

Etheridge SP, Bowles NE, Arrington CB, Pilcher T, Rope A, Wilde AA, Alders M, Saarel EV, Tavernier R, Timothy KW, Tristani-Firouzi M. Etheridge SP, et al. Among authors: arrington cb. Am J Med Genet A. 2011 Oct;155A(10):2578-83. doi: 10.1002/ajmg.a.34223. Epub 2011 Sep 9. Am J Med Genet A. 2011. PMID: 21910241

9

The role of screening and prophylactic surgery for malrotation in heterotaxy patients.

Elder CT, Metzger R, Arrington C, Rollins M, Scaife E. Elder CT, et al. J Pediatr Surg. 2014 Dec;49(12):1746-8. doi: 10.1016/j.jpedsurg.2014.09.007. Epub 2014 Nov 13. J Pediatr Surg. 2014. PMID: 25487475

10

White matter lesions in children and adolescents with migraine.

Candee MS, McCandless RT, Moore KR, Arrington CB, Minich LL, Bale JF Jr. Candee MS, et al. Among authors: arrington cb. Pediatr Neurol. 2013 Dec;49(6):393-6. doi: 10.1016/j.pediatrneurol.2013.08.025. Epub 2013 Oct 2. Pediatr Neurol. 2013. PMID: 24095578

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