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1 . Periodical
CDKN1Cp57Kip2 analysis in Beckwith–Wiedemann syndrome BWS patients: Genotype–phenotype correlations, novel mutations, and polymorphismsHow to cite this article: Romanelli V, Belinchón A, BenitoSanz S, MartínezGlez V, GraciaBouthelier R, Heath KE, CamposBarros A, GarcíaMiñaur S, Fernandez L, Meneses H, LópezSiguero JP, GuillénNavarro E, GómezPuertas P, Wesselink JJ, Mercado G, EstebanMarfil V, Palomo R, Mena R, Sánchez A, del Campo M, Lapunzina P. 2010. CDKN1Cp57Kip2 analysis in Beckwith–Wiedemann syndrome BWS patients: Genotype–phenotype correlations, novel mutations, and polymorphisms. Am J Med Genet Part A 152A:1390–1397.
- 저자
- by Romanelli, Valeria; Belinchón, Alberta; BenitoSanz, Sara; MartínezGlez, Victor; GraciaBouthelier, Ricardo, et al.
- 소스
- American Journal of Medical Genetics. Part A; June 2010, Vol. 152 Issue: 6 p1390-1397, 8p