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413T Hanwoo-specific structural variations generate genomic diversity in the cattle genome.

414F Study of G2 phase cell cycle arrest and its application in mediating ) genome.

396F Single cell allele specific expression (ASE) in T21 and common trisomies: A novel approach to understand Down syndrome and gene dosage effects in aneuploidies.

397W A sequential screening strategy for efficient rare gene discovery in small families.

409W Complementary long and short-read sequencing techniques identify rearrangement structures and concurrent single nucleotide variant formation on chromosome 17p11.2.

410T Method for deciding detection limit of droplet digital PCR for rare mutations.

374T‡ High-throughput functional genomic assessment of known and novel missense variants to support clinical diagnostic interpretation.

411F Targeted next-generation sequencing for identifying genes related to horse temperament.

412W Cross-tissue protein expression and genetic regulation of transcription factors and cell signaling genes in enhancing Genotype-Tissue Expression (e GTEx) samples.

377T Primary bilateral macronodular adrenocortical hyperplasia due to mutations in : New mutations in humans and modeling in zebrafish.

378F Cargo of mi RNAs from synovial fluid exosomes contributes to pathogenesis of primary osteoarthritis.

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403W Chitinases m RNA levels quantified by q PCR in crab-eating monkey tissues.

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