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144. Tracking of the origin of recurrent mutations of the BRCA1 and BRCA2 genes in the North-East of Italy and improved mutation analysis strategy. Issue 1 (December 2016)

145. Two hits in one: whole genome sequencing unveils LIG4 syndrome and urofacial syndrome in a case report of a child with complex phenotype. Issue 1 (December 2016)

146. Two novel MYH7 proline substitutions cause Laing Distal Myopathy-like phenotypes with variable expressivity and neck extensor contracture. Issue 1 (December 2016)

147. Utilization of amplicon-based targeted sequencing panel for the massively parallel sequencing of sporadic hearing impairment patients from Saudi Arabia. Issue 1 (October 2016)

149. Variants in CXCR4 associate with juvenile idiopathic arthritis susceptibility. Issue 1 (December 2016)

150. Variants of PLCXD3 are not associated with variant or sporadic Creutzfeldt-Jakob disease in a large international study. Issue 1 (December 2016)