Connection

CHENG CAMERON YIN to High-Throughput Nucleotide Sequencing

This is a "connection" page, showing publications CHENG CAMERON YIN has written about High-Throughput Nucleotide Sequencing.
  1. STAT5B mutations in myeloid neoplasms differ by disease subtypes but characterize a subset of chronic myeloid neoplasms with eosinophilia and/or basophilia. Haematologica. 2024 06 01; 109(6):1825-1835.
    View in: PubMed
    Score: 0.123
  2. Identification of a novel fusion gene, IRF2BP2-RARA, in acute promyelocytic leukemia. J Natl Compr Canc Netw. 2015 Jan; 13(1):19-22.
    View in: PubMed
    Score: 0.064
  3. Noninvasive prenatal diagnosis for Duchenne muscular dystrophy based on the direct haplotype phasing. Prenat Diagn. 2020 07; 40(8):918-924.
    View in: PubMed
    Score: 0.023
  4. Whole-exome sequencing as a powerful tool for identifying genetic causes in a patient with POLG-related disorders and phenylketonuria. J Int Med Res. 2019 Mar; 47(3):1387-1394.
    View in: PubMed
    Score: 0.021
Connection Strength

The connection strength for concepts is the sum of the scores for each matching publication.

Publication scores are based on many factors, including how long ago they were written and whether the person is a first or senior author.