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Journal Abstract Search
473 related items for PubMed ID: 16575195
1. New chromosome 11p15 epigenotypes identified in male monozygotic twins with Beckwith-Wiedemann syndrome. Smith AC, Rubin T, Shuman C, Estabrooks L, Aylsworth AS, McDonald MT, Steele L, Ray PN, Weksberg R. Cytogenet Genome Res; 2006; 113(1-4):313-7. PubMed ID: 16575195 [Abstract] [Full Text] [Related]
3. Beckwith-Wiedemann syndrome. Weksberg R, Shuman C, Smith AC. Am J Med Genet C Semin Med Genet; 2005 Aug 15; 137C(1):12-23. PubMed ID: 16010676 [Abstract] [Full Text] [Related]
6. Discordant KCNQ1OT1 imprinting in sets of monozygotic twins discordant for Beckwith-Wiedemann syndrome. Weksberg R, Shuman C, Caluseriu O, Smith AC, Fei YL, Nishikawa J, Stockley TL, Best L, Chitayat D, Olney A, Ives E, Schneider A, Bestor TH, Li M, Sadowski P, Squire J. Hum Mol Genet; 2002 May 15; 11(11):1317-25. PubMed ID: 12019213 [Abstract] [Full Text] [Related]
8. Non-random X chromosome inactivation in an affected twin in a monozygotic twin pair discordant for Wiedemann-Beckwith syndrome. Orstavik RE, Tommerup N, Eiklid K, Orstavik KH. Am J Med Genet; 1995 Mar 27; 56(2):210-4. PubMed ID: 7625447 [Abstract] [Full Text] [Related]
20. Maternal Hypomethylation of KvDMR in a Monozygotic Male Twin Pair Discordant for Beckwith-Wiedemann Syndrome. Elalaoui SC, Garin I, Sefiani A, Perez de Nanclares G. Mol Syndromol; 2014 Jan 27; 5(1):41-6. PubMed ID: 24550765 [Abstract] [Full Text] [Related] Page: [Next] [New Search]