Publicaciones

Developmental pathogenesis of short palpebral fissure length in children with fetal alcohol syndrome

Agosto 1, 2009

Jones KL, Hoyme HE, Robinson LK, del Campo M, Manning MA, Bakhireva LN, Prewitt LM, Chambers CD. Birth Defects Res A Clin Mol Teratol. 2009 Aug;85(8):695

Unusual four-generation chromosome-22 rearrangement: when “normality” masks abnormality

Julio 1, 2009

Nevado J, de Torres ML, Fernández L, Mori MA, Villa A, Palomares M, García-Santiago F, Mansilla E, García-Miñaur S, Delicado A, Lapunzina P. Am J Med Genet A. 2009 Jul;149A(7):1561-4. No abstract available

Carrier frequency of SMA by quantitative analysis of the SMN1 deletion in the Iranian population

Junio 1, 2009

Hasanzad M, Azad M, Kahrizi K, Saffar BS, Nafisi S, Keyhanidoust Z, Azimian M, Refah AA, Also E, Urtizberea JA, Tizzano EF, Najmabadi H. Eur J Neurol. 2010 Jan;17(1):160-2. Epub 2009 Jun 15

Association of common copy number variants at the glutathione S-transferase genes and rare novel genomic changes with schizophrenia

Junio 1, 2009

Rodríguez-Santiago B, Brunet A, Sobrino B, Serra-Juhé C, Flores R, Armengol L, Vilella E, Gabau E, Guitart M, Guillamat R, Martorell L, Valero J, Gutiérrez-Zotes A, Labad A, Carracedo A, Estivill X, Pérez-Jurado LA. Mol Psychiatry. 2010 Oct;15(10):1023-33. Epub 2009 Jun 16

Publicaciones

Orden según fecha de publicación:

Developmental pathogenesis of short palpebral fissure length in children with fetal alcohol syndrome

Unusual four-generation chromosome-22 rearrangement: when “normality” masks abnormality

Carrier frequency of SMA by quantitative analysis of the SMN1 deletion in the Iranian population

Association of common copy number variants at the glutathione S-transferase genes and rare novel genomic changes with schizophrenia