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13. Prader-Willi and Angelman syndromes: update on genetic mechanisms and diagnostic complexities. Khan NL; Wood NW Curr Opin Neurol; 1999 Apr; 12(2):149-54. PubMed ID: 10226746 [TBL] [Abstract][Full Text] [Related]
14. Potential pitfall in Prader-Willi syndrome and Angelman syndrome molecular diagnosis. Cuisset L; Vasseur C; Jeanpierre M; Delpech M; Noséda G; Ponsot G Am J Med Genet; 1998 Dec; 80(5):543-5. PubMed ID: 9880230 [No Abstract] [Full Text] [Related]
15. The Prader-Willi syndrome and the Angelman syndrome. Vogels A; Fryns JP Genet Couns; 2002; 13(4):385-96. PubMed ID: 12558108 [TBL] [Abstract][Full Text] [Related]
16. Identification of cis- and trans-acting factors possibly modifying the risk of epimutations on chromosome 15. Zogel C; Böhringer S; Gross S; Varon R; Buiting K; Horsthemke B Eur J Hum Genet; 2006 Jun; 14(6):752-8. PubMed ID: 16596119 [TBL] [Abstract][Full Text] [Related]
17. [Molecular diagnosis of Prader-Willi and Angelman syndromes: methylation, cytogenetics and FISH analysis]. Santa María L; Curotto B; Cortés F; Rojas C; Alliende MA Rev Med Chil; 2001 Apr; 129(4):367-74. PubMed ID: 11413988 [TBL] [Abstract][Full Text] [Related]
19. 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; 50(1):11-20. PubMed ID: 17095305 [TBL] [Abstract][Full Text] [Related]
20. Genes for Prader Willi syndrome/Angelman syndrome and fragile X syndrome are homologous, with genetic imprinting and unstable trinucleotide repeats causing mental retardation, autism and aggression. Fischer KM Med Hypotheses; 1996 Oct; 47(4):289-98. PubMed ID: 8910878 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]