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Whole-exome sequencing reveals GPIHBP1 mutations in infantile colitis with severe hypertriglyceridemia.
Gonzaga-Jauregui C, Mir S, Penney S, Jhangiani S, Midgen C, Finegold M, Muzny DM, Wang M, Bacino CA, Gibbs RA, Lupski JR, Kellermayer R, Hanchard NA. Gonzaga-Jauregui C, et al. Among authors: midgen c. J Pediatr Gastroenterol Nutr. 2014 Jul;59(1):17-21. doi: 10.1097/MPG.0000000000000363. J Pediatr Gastroenterol Nutr. 2014. PMID: 24614124 Free PMC article.
Congenital Myenteric Hypoganglionosis.
Kapur RP, Bellizzi AM, Bond S, Chen H, Han JS, LeGallo RD, Midgen C, Poulin AA, Uddin N, Warren M, Velázquez Vega JE, Zuppan CW. Kapur RP, et al. Among authors: midgen c. Am J Surg Pathol. 2021 Aug 1;45(8):1047-1060. doi: 10.1097/PAS.0000000000001670. Am J Surg Pathol. 2021. PMID: 33492848
Painless nodule on the external ear.
Phipps K, Havenga M, Midgen C, Bezuhly M. Phipps K, et al. Among authors: midgen c. Pediatr Dermatol. 2015 May-Jun;32(3):417-8. doi: 10.1111/pde.12503. Pediatr Dermatol. 2015. PMID: 25996673 No abstract available.
14 results