C. Lin

发表

Lack of mutations in CYP2D6 and CYP27 in patients with apparent deficiency of vitamin D 25-hydroxylase.

W. Miller, M. Abdullah, Chin Lin, 2003, Molecular genetics and metabolism.

Genetics of Vitamin D 1α-Hydroxylase Deficiency in 17 Families

Jonathan T. Wang, M. Labuda, W. Miller, 1998 .

Genome-Wide Structural Variation Detection by Genome Mapping on Nanochannel Arrays

Kevin Y. Yip, Jacob J. K. Wu, A. Pang, 2015, Genetics.

A Hybrid Approach for de novo Human Genome Sequence Assembly and Phasing

P. Kwok, J. Wall, P. Marks, 2016, Nature Methods.

Genomic regions associated with microdeletion/microduplication syndromes exhibit extreme diversity of structural variation.

U. Surti, T. Shaikh, P. Kwok, 2021, Genetics.

Genome mapping on nanochannel arrays for structural variation analysis and sequence assembly

P. Kwok, N. Nagarajan, M. Xiao, 2012, Nature Biotechnology.

Genome mapping resolves structural variation within segmental duplications associated with microdeletion/microduplication syndromes

T. Shaikh, P. Kwok, C. Chu, 2020, bioRxiv.

OMSV enables accurate and comprehensive identification of large structural variations from nanochannel-based single-molecule optical maps

Kevin Y. Yip, Iris K. Pang, P. Kwok, 2017, bioRxiv.

Genome maps across 26 human populations reveal population-specific patterns of structural variation

Pui-Yan Kwok, Catherine Chu, Kevin Y Yip, 2019, Nature Communications.

Finished sequence and assembly of the DUF1220-rich 1q21 region using a haploid human genome

T. Graves, R. Wilson, J. Sikela, 2014, BMC Genomics.

Mutation of proline 409 to arginine in the meander region of cytochrome p450c17 causes severe 17 alpha-hydroxylase deficiency.

K. Choy, J. Honour, W. Miller, 2001, Molecular genetics and metabolism.