Borck, G., Redon, R., Sanlaville, D., Rio, M., Prieur, M., Lyonnet, S., . . . Cormier-Daire, V. (2004). NIPBL mutations and genetic heterogeneity in Cornelia de Lange syndrome. BMJ Group.
Citação norma ChicagoBorck, G., et al. NIPBL Mutations and Genetic Heterogeneity in Cornelia De Lange Syndrome. BMJ Group, 2004.
ציטוט MLABorck, G., et al. NIPBL Mutations and Genetic Heterogeneity in Cornelia De Lange Syndrome. BMJ Group, 2004.
אזהרה: ציטוטים אלה לעיתים לא מדויקים ב 100%.