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Journal of Medical Genetics|April 10, 2009
Mutations in DNAH5 account for only 15% of a non-preselected cohort of patients with primary ciliary dyskinesiaM Failly, L Bartoloni, A Letourneau, et al.Cytogenetics and Cell Genetics|November 4, 2000
No deleterious mutations in the FOXJ1 (alias HFH-4) gene in patients with primary ciliary dyskinesia (PCD)A K Maiti, L Bartoloni, H M Mitchison, et al.Genomics|March 15, 2001
Axonemal beta heavy chain dynein DNAH9: cDNA sequence, genomic structure, and investigation of its role in primary ciliary dyskinesiaL Bartoloni, J L Blouin, A K Maiti, et al.European Journal of Human Genetics : EJHG|April 11, 2000
Primary ciliary dyskinesia: a genome-wide linkage analysis reveals extensive locus heterogeneityJ L Blouin, M Meeks, U Radhakrishna, et al.Pageof 4