Human Genome Epidemiology Literature Finder
Records 1 - 5 (of 5 Records) |
Query Trace: Counseling and KCNJ11[original query] |
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Mutation spectra of ABCC8 gene in Spanish patients with Hyperinsulinism of Infancy (HI). Human mutation 2006 1 27 (2): 214. Fernández-Marmiesse Ana, Salas Antonio, Vega Ana, Fernández-Lorenzo José Ramón, Barreiro Jesús, Carracedo Ang |
ABCC8 mutation allele frequency in the Ashkenazi Jewish population and risk of focal hyperinsulinemic hypoglycemia. Genetics in medicine : official journal of the American College of Medical Genetics 2011 Oct 13 (10): 891-4. Glaser Benjamin, Blech Ilana, Krakinovsky Yocheved, Ekstein Josef, Gillis David, Mazor-Aronovitch Kineret, Landau Heddy, Abeliovich Dvor |
Novel ABCC8 (SUR1) gene mutations in Asian Indian children with congenital hyperinsulinemic hypoglycemia. Annals of human genetics 2014 Sep 78 (5): 311-9. Jahnavi Suresh, Poovazhagi Varadarajan, Kanthimathi Sekar, Balamurugan Kandasamy, Bodhini Dhanasekaran, Yadav Jaivinder, Jain Vandana, Khadgawat Rajesh, Sikdar Mahuya, Bhavatharini Ayurchelvan, Das Ashok Kumar, Kaur Tanvir, Mohan Viswanathan, Radha Venkates |
Uncovering the molecular pathogenesis of congenital hyperinsulinism by panel gene sequencing in 32 Chinese patients. Molecular genetics & genomic medicine 2015 Nov 3 (6): 526-36. Fan Zi-Chuan, Ni Jin-Wen, Yang Lin, Hu Li-Yuan, Ma Si-Min, Mei Mei, Sun Bi-Jun, Wang Hui-Jun, Zhou Wen-H |
Clinical and molecular characteristics of infantile-onset diabetes mellitus in Egypt. Annals of pediatric endocrinology & metabolism 2022 2 27 (3): 214-222. Abdelmeguid Yasmine, Mowafy Ehsan Wafa, Marzouk Iman, Franco Elisa De, ElSayed Shaym |
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