Ruth J. Lin

The diversity of hereditary neuromuscular diseases: Experiences from molecular diagnosis.

Y. Chien, W. Hwu, Wang-Tso Lee, 2022, Journal of the Formosan Medical Association = Taiwan yi zhi.

Terminal deletion of 6p results in a recognizable phenotype

H. Hoyme, L. Hudgins, A. Cherry, 2005, American journal of medical genetics. Part A.

Contrast enema in children with Henoch-Schönlein purpura.

J. Schwab, E. Benya, Ruth J. Lin, 2005, Journal of pediatric surgery.

A novel His158Arg mutation in TIMP3 causes a late-onset form of Sorsby fundus dystrophy.

M. Blumenkranz, J. Binkley, D. Vollrath, 2006, American journal of ophthalmology.