Search Results - "Law, Fian BF"

Abstract P6-08-13: Personalized and cost-effective detection of copy number variants by molecular-barcode next-generation sequencing and long-read nanopore sequencing by Kwong, Ava, Au, Chun H, Ho, Dona N, Wong, Elaine YL, Chung, Yvonne, Law, Fian BF, Ho, Cecilia YS, Chen, Jiawei, Cheuk, Isabella W, Shin, Vivian Y, Chan, Tsun L, Ngan, Hextan YS, Ma, Edmond SK

“…Background: Germline copy number variants (CNV) of hereditary breast and ovarian cancer genes are a known class of clinically significant mutations. However,…”
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A novel de novo BRCA1 mutation in a Chinese woman with early onset breast cancer by Kwong, Ava, Ng, Enders K. O., Tang, Edmund Y. H., Wong, Chris L. P., Law, Fian B. F., Leung, Candy P. H., Chan, Aaron, Cheung, M. T., To, M. Y., Ma, Edmond S. K., West, Dee W., Ford, James M.

“…Germline mutations in the two breast cancer susceptibility genes, BRCA1 and BRCA2 account for a significant portion of hereditary breast/ovarian cancer. De…”
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