2. Screening and polymorphism analysis of 2.XNP gene polymorphism sites, Acta Genetica Sinica 2002,29 (3): 201-205.
3. Linkage and mutation analysis between Smith-Fineman-Myers syndrome and GRIA3 gene, Acta Genetica Sinica, 200 1, 28 (1 1): 985-990.
4. LDL receptor-related protein 5 (LRP5) affects bone growth and eye development, Cell, 200 1, 107:5 13-523.
5. Construction of human fetal bone and joint cDNA library, China Journal of Medical Genetics 200 1, 18 (1): 24-27.
6. The gene of Smith-Fineman-Myers syndrome is located in Xq25, China Journal of Medical Genetics 1999, 16 (5): 277-280.
Type B short finger deformity: clinical description, gene mapping of chromosome 9q, and evidence of common ancestor mutation. Am J Hum Genet， 1999，64: 570-577
The heterozygous mutation of the gene encoding cephalin affects the morphogenesis of human joints. Natural Genetics, 2 1, 1999 March, 302-304
9. YAC terminal was isolated and analyzed by reverse PCR. China Journal of Medical Genetics,1999; 16( 1):44-46