APA
Romanelli V., Belinchón A., Benito-Sanz S., Martínez-Glez V., Gracia-Bouthelier R., Heath K. E., Campos-Barros A., García-Miñaur S., Fernandez L., Meneses H., López-Siguero J. P., Guillén-Navarro E., Gómez-Puertas P., Wesselink J., Mercado G., Esteban-Marfil V., Palomo R., Mena R., Sánchez A., Del Campo M. & Lapunzina P. (20100830). CDKN1C (p57(Kip2)) analysis in Beckwith-Wiedemann syndrome (BWS) patients: Genotype-phenotype correlations, novel mutations, and polymorphisms. : American journal of medical genetics. Part A.
Chicago
Romanelli Valeria, Belinchón Alberta, Benito-Sanz Sara, Martínez-Glez Victor, Gracia-Bouthelier Ricardo, Heath Karen E, Campos-Barros Angel, García-Miñaur Sixto, Fernandez Luís, Meneses Heloisa, López-Siguero Juan Pedro, Guillén-Navarro Encarna, Gómez-Puertas Paulino, Wesselink Jan-Jaap, Mercado Graciela, Esteban-Marfil Victoria, Palomo Rebeca, Mena Rocío, Sánchez Aurora, Del Campo Miguel and Lapunzina Pablo. 20100830. CDKN1C (p57(Kip2)) analysis in Beckwith-Wiedemann syndrome (BWS) patients: Genotype-phenotype correlations, novel mutations, and polymorphisms. : American journal of medical genetics. Part A.
Harvard
Romanelli V., Belinchón A., Benito-Sanz S., Martínez-Glez V., Gracia-Bouthelier R., Heath K. E., Campos-Barros A., García-Miñaur S., Fernandez L., Meneses H., López-Siguero J. P., Guillén-Navarro E., Gómez-Puertas P., Wesselink J., Mercado G., Esteban-Marfil V., Palomo R., Mena R., Sánchez A., Del Campo M. and Lapunzina P. (20100830). CDKN1C (p57(Kip2)) analysis in Beckwith-Wiedemann syndrome (BWS) patients: Genotype-phenotype correlations, novel mutations, and polymorphisms. : American journal of medical genetics. Part A.
MLA
Romanelli Valeria, Belinchón Alberta, Benito-Sanz Sara, Martínez-Glez Victor, Gracia-Bouthelier Ricardo, Heath Karen E, Campos-Barros Angel, García-Miñaur Sixto, Fernandez Luís, Meneses Heloisa, López-Siguero Juan Pedro, Guillén-Navarro Encarna, Gómez-Puertas Paulino, Wesselink Jan-Jaap, Mercado Graciela, Esteban-Marfil Victoria, Palomo Rebeca, Mena Rocío, Sánchez Aurora, Del Campo Miguel and Lapunzina Pablo. CDKN1C (p57(Kip2)) analysis in Beckwith-Wiedemann syndrome (BWS) patients: Genotype-phenotype correlations, novel mutations, and polymorphisms. : American journal of medical genetics. Part A. 20100830.