Ernesto Solís-Añez

Detección de Portadoras de Distrofia Muscular Duchenne/Becker a través del Análisis de Loci STRs Ligados al Gen de la Distrofina en Familias Venezolanas

A. Rojas-Atencio, A. Morales-Machín, William Zabala-Fernández, 2002 .

PAGOD syndrome and vascular anomalies: is a defect embryonic angiogenesis? A case report and review.

A. Morales-Machín, W. Delgado-Luengo, Ernesto Solís-Añez, 2016, Investigacion clinica.

Petty–Laxova–Wiedemann progeroid syndrome: Further phenotypical delineation and confirmation of a rare syndrome of premature aging

E. Petty, A. Morales-Machín, William Zabala-Fernández, 2009, American journal of medical genetics. Part A.

[C677T polymorphism of the methylentetrahydrofolate reductase gene as risk factor in women with recurrent abortion].

W. Zabala, A. Morales-Machín, F. Alvarez, 2009, Investigación Clínica.

Huntington’s Disease in Chile: Epidemiological and Genetic Aspects

Olga Benavides, P. Salles, Ernesto Solís-Añez, 2023, Neuroepidemiology.