A. Salmi

Mutation Spectrum of Dystrophin Gene in Malaysian Patients with Duchenne/Becker Muscular Dystrophy

M. Matsuo, T. H. Sasongko, B. Zilfalil, 2013, Journal of neurogenetics.

Permissibility of prenatal diagnosis and abortion for fetuses with severe genetic disorder: type 1 spinal muscular atrophy

T. H. Sasongko, B. Zilfalil, M. Albar, 2010, Annals of Saudi medicine.

Two closely spaced nonsense mutations in the DMD gene in a Malaysian family.

Y. Takeshima, M. Matsuo, T. H. Sasongko, 2011, Molecular genetics and metabolism.

Two novel gross deletions of TSC2 in Malaysian patients with tuberous sclerosis complex and TSC2/PKD1 contiguous deletion syndrome.

T. H. Sasongko, F. Hayati, L. Ngu, 2014, Japanese journal of clinical oncology.

A new method for FMR1 gene methylation screening by multiplex methylation-specific real-time polymerase chain reaction.

B. Zilfalil, P. Limprasert, R. Ankathil, 2011, Genetic testing and molecular biomarkers.