III Jornada de primavera de dismorfología de la SEGCD
Viernes 1 de abril – 9:30 a 14:00 horas
FORMATO VIRTUAL
Orden según fecha de publicación:
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 Jan-Feb;50(1):11-20. Epub 2006 Oct 10
Intrachromosomal partial triplication of chromosome 13 secondary to a paternal duplication with mild phenotypic effect
López-Expósito I, Bafalliu JA, Santos M, Fuster C, Puche-Mira A, Guillén-Navarro E. Am J Med Genet A. 2008 May 1;146A(9):1190-4
Intrauterine growth retardation, duodenal and extrahepatic biliary atresia, hypoplastic pancreas and other intestinal anomalies: further evidence of the Martínez-Frías syndrome
Galán-Gómez E, Sánchez EB, Arias-Castro S, Cardesa-García JJ. Eur J Med Genet. 2007 Mar-Apr;50(2):144-8
