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.