Prenatal diagnosis of campomelic dysplasia with three-dimensional ultrasound [1]

由 P. Promsonthi, D. Wattanasirichaigoon
出版 2018

Case report of a Thai male cystic fibrosis patinet with the 1898+ 1G-->T splicing mutation in the CFTR gene: a review of East Asian cases. Mutations in brief no. 196. Online.

由 S. Suwanjutha, N. N. Huang, D. Wattanasirichaigoon, T. Sura, A. Harris, M. Macek
出版 2018

Molecular characterization of type 3 (neuronopathic) Gaucher disease in Thai patients

由 P. Suwannarat, S. Keeratichamroen, D. Wattanasirichaigoon, L. Ngiwsara, J. R K Cairns, J. Svasti, A. Visudtibhan, S. Pangkanon
出版 2018

Molecular analysis of the iduronate-2-sulfatase gene in Thai patients with Hunter syndrome

由 S. Keeratichamroen, J. R Ketudat Cairns, D. Wattanasirichaigoon, P. Wasant, L. Ngiwsara, P. Suwannarat, S. Pangkanon, J. Kuptanon, P. Tanpaiboon, T. Rujirawat, S. Liammongkolkul, J. Svasti
出版 2018

Molecular analysis of the iduronate-2-sulfatase gene in Thai patients with Hunter syndrome

由 S. Keeratichamroen, J. R Ketudat Cairns, D. Wattanasirichaigoon, P. Wasant, L. Ngiwsara, P. Suwannarat, S. Pangkanon, J. Kuptanon, P. Tanpaiboon, T. Rujirawat, S. Liammongkolkul, J. Svasti
出版 2018