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2. Familial hyperinsulinism with nesidioblastosis of the pancreas: further evidence for autosomal recessive inheritance. Moreno LA, Turck D, Gottrand F, Fabre M, Manouvrier-Hanu S, Farriaux JP. Am J Med Genet; 1989 Dec; 34(4):584-6. PubMed ID: 2624273 [Abstract] [Full Text] [Related]
7. Loss of imprinted genes and paternal SUR1 mutations lead to hyperinsulinism in focal adenomatous hyperplasia. Fournet JC, Verkarre V, De Lonlay P, Rahier J, Brunelle F, Robert JJ, Nihoul-Fékété C, Saudubray JM, Junien C. Ann Endocrinol (Paris); 1998 Dec; 59(6):485-91. PubMed ID: 10189991 [Abstract] [Full Text] [Related]
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20. A recessive contiguous gene deletion causing infantile hyperinsulinism, enteropathy and deafness identifies the Usher type 1C gene. Bitner-Glindzicz M, Lindley KJ, Rutland P, Blaydon D, Smith VV, Milla PJ, Hussain K, Furth-Lavi J, Cosgrove KE, Shepherd RM, Barnes PD, O'Brien RE, Farndon PA, Sowden J, Liu XZ, Scanlan MJ, Malcolm S, Dunne MJ, Aynsley-Green A, Glaser B. Nat Genet; 2000 Sep 07; 26(1):56-60. PubMed ID: 10973248 [Abstract] [Full Text] [Related] Page: [Next] [New Search]