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You searched for: Author/Creator Erzurumluoglu, A. Mesut

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1. Associations of Y chromosomal haplogroups with cardiometabolic risk factors and subclinical vascular measures in males during childhood and adolescence. (July 2018)

2. Identifying Highly Penetrant Disease Causal Mutations Using Next Generation Sequencing: Guide to Whole Process. (6th April 2015)

4. Nonsense Mutation in Coiled‐Coil Domain Containing 151 Gene (CCDC151) Causes Primary Ciliary Dyskinesia. Issue 12 (December 2014)

5. Novel Blood Pressure Locus and Gene Discovery Using Genome-Wide Association Study and Expression Data Sets From Blood and the Kidney. Issue 3 (September 2017)