Chenyan Wu

发表

No evidence for linkage of familial hypertrophic cardiomyopathy and chromosome 14q1 locus D14S26 in a chinese family: evidence for genetic heterogeneity

Y. Ko, T. Tang, C. Liew, 1992, Human Genetics.

Dysferlin, a novel skeletal muscle gene, is mutated in Miyoshi myopathy and limb girdle muscular dystrophy

Pieter J. de Jong, Saeed Bohlega, Jing Liu, 1998, Nature Genetics.

DOP-vector PCR: a method for rapid isolation and sequencing of insert termini from PAC clones

Chenyan Wu, Pieter J. de Jong, Shigui Zhu, 1996, Nucleic Acids Res..

SPTLC1 is mutated in hereditary sensory neuropathy, type 1

Robert H. Brown, P. Jong, Margaret D. Scheffler, 2001, Nature Genetics.

Genetic, physical, and comparative map of the subtelomeric region of mouse Chromosome 4

P. Jong, G. Beauchamp, D. Reed, 2001, Mammalian Genome.

Positional cloning of the combined hyperlipidemia gene Hyplip1

P. D. de Jong, J. Catanese, A. Lusis, 2002, Nature genetics.

Positional cloning of the mouse saccharin preference (Sac) locus.

P. D. de Jong, G. Beauchamp, D. Reed, 2001, Chemical senses.

A bacterial artificial chromosome library for sequencing the complete human genome.

P. D. de Jong, K. Osoegawa, J. Catanese, 2001, Genome research.