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Breast Cancer Research and Treatment|September 2, 2016
Ready to clone: CNV detection and breakpoint fine-mapping in breast and ovarian cancer susceptibility genes by high-resolution array CGHKarl Hackmann, Franziska Kuhlee, Elitza Betcheva-Krajcir, et al.Breast Cancer Research and Treatment|May 30, 2015
HBOC multi-gene panel testing: comparison of two sequencing centersChristopher Schroeder, Ulrike Faust, Marc Sturm, et al.Plos One|September 24, 2020
Correction: Diagnostic value of partial exome sequencing in developmental disordersLaura Gieldon, Luisa Mackenroth, Anne-Karin Kahlert, et al.Plos One|August 10, 2018
Diagnostic value of partial exome sequencing in developmental disordersLaura Gieldon, Luisa Mackenroth, Anne-Karin Kahlert, et al.Plos Genetics|August 10, 2016
Identification and Functional Testing of ERCC2 Mutations in a Multi-national Cohort of Patients with Familial Breast- and Ovarian CancerAndreas Rump, Anna Benet-Pages, Steffen Schubert, et al.Science Translational Medicine|September 5, 2014
Effective diagnosis of genetic disease by computational phenotype analysis of the disease-associated genomeTomasz Zemojtel, Sebastian Köhler, Luisa Mackenroth, et al.Journal of Medical Genetics|March 9, 2017
PBX1 haploinsufficiency leads to syndromic congenital anomalies of the kidney and urinary tract (CAKUT) in humansPauline Le Tanno, Julie Breton, Marie Bidart, et al.Pageof 2