Estudio de tres loci hipervariables en población mixta chilena

by Novoa C,M del Rosario, Labbé C,Carolina, Jorquera G,Hugo, Moreno Ch,Fabián, Aguirre M,M Eugenia, Cifuentes O,Lucía
Published 2001

Búsqueda de afecciones genéticas como etiología de déficit intelectual en individuos que asisten a escuelas de educación especial

by Alliende,M Angélica, Cámpora,Laura, Curotto,Bianca, Toro,Jessica, Valiente,Alf, Castillo,Marcela, Cortés,Fanny, Trigo,César, Alvarado,Cecilia, Silva,Manuel, Caru,Margarita
Published 2008

Genetic Variants and Clinical Phenotypes in Korean Patients With Hereditary Hemorrhagic Telangiectasia

by Bo-Gyeong Kim, Joo-hyun Jung, Mi-Jung Kim, Eun-Hye Moon, Jae-Hwan Oh, Jung-Woo Park, Heung-Eog Cha, Ju-Hyun Kim, Yoon-Jae Kim, Jun-Won Chung, Ki-Baik Hahm, Hong-Ryul Jin, Yong-Ju Jang, Sung Wan Kim, Seung-Kyu Chung, Dae-Woo Kim, Young Jae Lee, Seon-Tae Kim
Published 2021

Concurrent Newborn Hearing and Genetic Screening in a Multi-Ethnic Population in South China

by Xiangrong Tang, Lihua Liu, Sulan Liang, Meie Liang, Tao Liao, Shiqiang Luo, Tizhen Yan, Jianping Chen
Published 2021

Management of Hypertrophic Cardiomyopathy

by Alan D. Enriquez, Martin E. Goldman
Published 2014

Identification of the Cell-Surface Protease ADAM9 as an Entry Factor for Encephalomyocarditis Virus

by Jim Baggen, Hendrik Jan Thibaut, Daniel L. Hurdiss, Maryam Wahedi, Caleb D. Marceau, Arno L. W. van Vliet, Jan E. Carette, Frank J. M. van Kuppeveld
Published 2019

The (re)discovery of tumor-intrinsic determinants of immune sensitivity by functional genetic screens

by D.W. Vredevoogd, G. Apriamashvili, D.S. Peeper
Published 2021