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562. Whole genome sequencing identifies rare genetic variants in familial pancreatic cancer patients. (21st March 2022)

565. Wilson Disease Mutation Pattern with Genotype‐Phenotype Correlations from Western India: Confirmation of p.C271* as a Common Indian Mutation and Identification of 14 Novel Mutations. (2nd April 2013)

568. Y‐Chromosomal Lineages of Latvians in the Context of the Genetic Variation of the Eastern‐Baltic Region. (28th September 2015)