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Journal of Human Genetics|October 23, 2015
Tumor-suppressive microRNAs (miR-26a/b, miR-29a/b/c and miR-218) concertedly suppressed metastasis-promoting LOXL2 in head and neck squamous cell carcinomaIchiro Fukumoto, Naoko Kikkawa, Ryosuke Matsushita, et al.Journal of Human Genetics|February 5, 2016
Charting the Y-chromosome ancestry of present-day Argentinean MennonitesUlises Toscanini, Francesca Brisighelli, Cintia Llull, et al.Journal of Human Genetics|February 26, 2016
NAT2 variants are associated with drug-induced liver injury caused by anti-tuberculosis drugs in Indonesian patients with tuberculosisRika Yuliwulandari, Retno Wilujeng Susilowati, Britanto Dani Wicaksono, et al.Journal of Human Genetics|February 26, 2016
Detection of high frequency of mutations in a breast and/or ovarian cancer cohort: implications of embracing a multi-gene panel in molecular diagnosis in IndiaAshraf U Mannan, Jaya Singh, Ravikiran Lakshmikeshava, et al.Journal of Human Genetics|February 26, 2016
The novel complex allele [A238V;F508del] of the CFTR gene: clinical phenotype and possible implications for cystic fibrosis etiological therapiesAnna Diana, Angela Maria Polizzi, Teresa Santostasi, et al.Journal of Human Genetics|August 28, 2015
Joint effect of the SMN2 and SERF1A genes on childhood-onset types of spinal muscular atrophy in Serbian patientsMiloš Brkušanin, Ana Kosać, Vladimir Jovanović, et al.Journal of Human Genetics|January 16, 2015
Exome sequencing identifies a novel CEACAM16 mutation associated with autosomal dominant nonsyndromic hearing loss DFNA4B in a Chinese familyHonghan Wang, Xinwei Wang, Chufeng He, et al.Journal of Human Genetics|January 9, 2015
Chinese homozygous Machado-Joseph disease (MJD)/SCA3: a case reportSheng Zeng, Junsheng Zeng, Miao He, et al.Journal of Human Genetics|January 9, 2015
Copy-number variations in Y-chromosomal azoospermia factor regions identified by multiplex ligation-dependent probe amplificationKazuki Saito, Mami Miyado, Yoshitomo Kobori, et al.Journal of Human Genetics|December 16, 2014
Severe phenotypes in a Charcot-Marie-Tooth 1A patient with PMP22 triplicationSung Min Kim, Jinho Lee, Bo Ram Yoon, et al.Pageof 352