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Journal Abstract Search
151 related items for PubMed ID: 33419637
1. Variance in the pathophysiological impact of the hemizygosity of gamma-aminobutyric acid type A receptor subunit genes between Prader-Willi syndrome and Angelman syndrome. Egawa K, Saitoh S, Asahina N, Shiraishi H. Brain Dev; 2021 Apr; 43(4):521-527. PubMed ID: 33419637 [Abstract] [Full Text] [Related]
5. Are Angelman and Prader-Willi syndromes more similar than we thought? Food-related behavior problems in Angelman, Cornelia de Lange, fragile X, Prader-Willi and 1p36 deletion syndromes. Welham A, Lau J, Moss J, Cullen J, Higgs S, Warren G, Wilde L, Marr A, Cook F, Oliver C. Am J Med Genet A; 2015 Mar; 167A(3):572-8. PubMed ID: 25691410 [Abstract] [Full Text] [Related]
15. Imprinting center analysis in Prader-Willi and Angelman syndrome patients with typical and atypical phenotypes. Camprubí C, Coll MD, Villatoro S, Gabau E, Kamli A, Martínez MJ, Poyatos D, Guitart M. Eur J Med Genet; 2007 May; 50(1):11-20. PubMed ID: 17095305 [Abstract] [Full Text] [Related]
16. Prevalence of Angelman syndrome and Prader-Willi syndrome in Estonian children: sister syndromes not equally represented. Oiglane-Shlik E, Talvik T, Zordania R, Põder H, Kahre T, Raukas E, Ilus T, Tasa G, Bartsch O, Väisänen ML, Ounap K. Am J Med Genet A; 2006 Sep 15; 140(18):1936-43. PubMed ID: 16906556 [Abstract] [Full Text] [Related]
20. Mechanisms of activation of the paternally expressed genes by the Prader-Willi imprinting center in the Prader-Willi/Angelman syndromes domains. Rabinovitz S, Kaufman Y, Ludwig G, Razin A, Shemer R. Proc Natl Acad Sci U S A; 2012 May 08; 109(19):7403-8. PubMed ID: 22529396 [Abstract] [Full Text] [Related] Page: [Next] [New Search]