S. Lin

An Effective Strategy of Using Molecular Testing to Screen Mentally Retarded Individuals for Fragile X Syndrome

C. Tzeng, Y. Jong, Shio‐Jean Lin, 2001, Diagnostic molecular pathology : the American journal of surgical pathology, part B.

Androgenetic alopecia in heterozygous carriers of a mutation in the human hairless gene.

R. Bergman, E. Sprecher, R. Szargel, 2000, Journal of the American Academy of Dermatology.

Clinical spectrum of enterovirus 71 infection in children in southern Taiwan, with an emphasis on neurological complications.

T. Yeh, J. Wang, Shih-Min Wang, 1999, Clinical infectious diseases : an official publication of the Infectious Diseases Society of America.

Y-chromosome microdeletion and its effect on reproductive decisions in taiwanese patients presenting with nonobstructive azoospermia.

Shio‐Jean Lin, P. Kuo, H. Sun, 2000, Urology.

Detection of Y-chromosomal DNA with marker chromosomes in Turner's syndrome.

C. Tzeng, P. Kuo, K. Huang, 1995, Journal of the Formosan Medical Association = Taiwan yi zhi.

Implication of screening for FMR1 and FMR2 gene mutation in individuals with nonspecific mental retardation in Taiwan.

C. Tzeng, H. Sun, S. Lin, 2000, Diagnostic molecular pathology : the American journal of surgical pathology, part B.