F. Martínez
发表
Prevalence and parental origin of de novo 1.5-Mb duplication in Charcot-Marie-Tooth disease type 1A.
F. Palau,
S. Bort,
F. Martínez,
1997,
American journal of human genetics.
I. Ferrer,
E. Farrero,
N. Sambuughin,
2004,
Journal of the Neurological Sciences.
J. Armstrong,
I. Ferrer,
M. Fardeau,
2007,
Neuromuscular Disorders.
Unclassifiable arrhythmic cardiomyopathy associated with Emery–Dreifuss caused by a mutation in FHL1
J. Guardiola,
M. Sabater-Molina,
J. Gimeno,
2016,
Clinical genetics.