Y. Du

发表

A Novel Tri-Allelic Insertion/Deletion Polymorphism in the Promoter of p21 and the Association with Gastric Cancer

Ning Wang, Yide A Jiang, Zhiqiang Chen, 2014 .

Differences in methylenetetrahydrofolate reductase genotype frequencies, between Whites and Blacks.

R. Stevenson, C. Schwartz, Y. Du, 1997, American journal of human genetics.

Structure of the human Lanosterol synthase gene and its analysis as a candidate for holoprosencephaly (HPE1).

S. Antonarakis, C. Rossier, M. Muenke, 1999 .

SHH mutation is associated with solitary median maxillary central incisor: a study of 13 patients and review of the literature.

M. Muenke, A. Bankier, R. Hall, 2001, American journal of medical genetics.

Regional localization of 725 human chromosome 7-specific yeast artificial chromosome clones.

S. Scherer, H. Heng, L. Tsui, 1994, Genomics.

Multiple exon screening using restriction endonuclease fingerprinting (REF): Detection of six novel mutations in the L1 cell adhesion molecule (L1CAM) gene

C. Schwartz, A. Srivastava, Yangzhu Du, 1998, Human mutation.

The genomic structure, chromosome location, and analysis of the human DKK1 head inducer gene as a candidate for holoprosencephaly

M. Muenke, E. Roessler, A. Glinka, 2000, Cytogenetic and Genome Research.

A transmembrane protein family gene signature for overall survival prediction in osteosarcoma

Xiaohui Zeng, Weiwei Yu, Y. Du, 2022, Frontiers in Genetics.

The site of a missense mutation in the extracellular Ig or FN domains of L1CAM influences infant mortality and the severity of X linked hydrocephalus.

C. Schwartz, R. Michaelis, Y. Du, 1998, Journal of medical genetics.