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2. Wolcott-Rallison syndrome due to the same mutation (W522X) in EIF2AK3 in two unrelated families and review of the literature. Ozbek MN; Senée V; Aydemir S; Kotan LD; Mungan NO; Yuksel B; Julier C; Topaloglu AK Pediatr Diabetes; 2010 Jun; 11(4):279-85. PubMed ID: 20202148 [TBL] [Abstract][Full Text] [Related]
3. Wolcott-Rallison Syndrome with Novel EIF2AK3 Gene Mutation. Gürbüz F; Yüksel B; Topaloğlu AK J Clin Res Pediatr Endocrinol; 2016 Dec; 8(4):496-497. PubMed ID: 27145240 [No Abstract] [Full Text] [Related]
4. THE 3rd W522X MUTATION IN EIF2AK3 GENE FROM TURKEY: A NEW PATIENT WITH WOLCOTT-RALLISON SYNDROME. Bahsi T; Unal A; Bakir A; Perçin EF Genet Couns; 2016; 27(3):411-418. PubMed ID: 30204972 [TBL] [Abstract][Full Text] [Related]
5. Wolcott-Rallison syndrome in two siblings with isolated central hypothyroidism. Bin-Abbas B; Al-Mulhim A; Al-Ashwal A Am J Med Genet; 2002 Aug; 111(2):187-90. PubMed ID: 12210348 [TBL] [Abstract][Full Text] [Related]
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7. Wolcott-Rallison syndrome due to a novel mutation (R491X) in EIF2AK3 gene. Mihci E; Türkkahraman D; Ellard S; Akçurin S; Bircan I J Clin Res Pediatr Endocrinol; 2012 Jun; 4(2):101-3. PubMed ID: 22672868 [TBL] [Abstract][Full Text] [Related]
8. Wolcott-Rallison Syndrome- Endocrinopathy with Recurrent Acute Liver Failure. Valamparampil JJ; Shanmugam N; Rela M Indian Pediatr; 2019 Dec; 56(12):1055-1056. PubMed ID: 31884440 [TBL] [Abstract][Full Text] [Related]
9. Os odontoideum in wolcott-rallison syndrome: a case series of 4 patients. Dias RP; Buchanan CR; Thomas N; Lim S; Solanki G; Connor SE; Barrett TG; Kapoor RR Orphanet J Rare Dis; 2016 Feb; 11():14. PubMed ID: 26860746 [TBL] [Abstract][Full Text] [Related]
14. Wolcott-Rallison syndrome: a clinical and genetic study of three children, novel mutation in EIF2AK3 and a review of the literature. Iyer S; Korada M; Rainbow L; Kirk J; Brown RM; Shaw N; Barrett TG Acta Paediatr; 2004 Sep; 93(9):1195-201. PubMed ID: 15384883 [TBL] [Abstract][Full Text] [Related]
15. Wolcott-Rallison syndrome in Iran: a common cause of neonatal diabetes. Asl SN; Vakili R; Vakili S; Soheilipour F; Hashemipour M; Ghahramani S; De Franco E; Yaghootkar H J Pediatr Endocrinol Metab; 2019 Jun; 32(6):607-613. PubMed ID: 31141482 [TBL] [Abstract][Full Text] [Related]
16. Short stature in child with early-onset diabetes. Hawkes CP; McGlacken-Byrne SM; Murphy NP Eur J Pediatr; 2013 Sep; 172(9):1255-7. PubMed ID: 23644647 [TBL] [Abstract][Full Text] [Related]
17. Wolcott-Rallison Syndrome With Different Clinical Presentations and Genetic Patterns in 2 Infants. Davoodi MA; Karamizadeh Z; Ghobadi F; Shokrpour N Health Care Manag (Frederick); 2018; 37(4):354-357. PubMed ID: 30234637 [TBL] [Abstract][Full Text] [Related]
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