Sporadic hypertrophic cardiomyopathy due to de novo myosin mutations.

Por Watkins, H, Thierfelder, L, Hwang, D S, McKenna, W, Seidman, J G, Seidman, C E
Publicado em 1992

Independent origin of identical beta cardiac myosin heavy-chain mutations in hypertrophic cardiomyopathy.

Por Watkins, H, Thierfelder, L, Anan, R, Jarcho, J, Matsumori, A, McKenna, W, Seidman, J G, Seidman, C E
Publicado em 1993

Prognostic implications of novel beta cardiac myosin heavy chain gene mutations that cause familial hypertrophic cardiomyopathy.

Por Anan, R, Greve, G, Thierfelder, L, Watkins, H, McKenna, W J, Solomon, S, Vecchio, C, Shono, H, Nakao, S, Tanaka, H
Publicado em 1994

A familial hypertrophic cardiomyopathy locus maps to chromosome 15q2.

Por Thierfelder, L, MacRae, C, Watkins, H, Tomfohrde, J, Williams, M, McKenna, W, Bohm, K, Noeske, G, Schlepper, M, Bowcock, A
Publicado em 1993

Familial Hypertrophic cardiomyopathy with Wolff-Parkinson-White syndrome maps to a locus on chromosome 7q3.

Por MacRae, C A, Ghaisas, N, Kass, S, Donnelly, S, Basson, C T, Watkins, H C, Anan, R, Thierfelder, L H, McGarry, K, Rowland, E
Publicado em 1995