Wijesinghe, S., De Silva, D., Samarasinghe, D. and Irugalbandara, S., 2022. Arterial tortuosity syndrome: A rare inherited form of connective tissue disorder with SLR2A10 gene mutation. Sri Lanka Journal of Child Health, 51(1), pp.142–145. DOI: http://doi.org/10.4038/sljch.v51i1.10023

Wijesinghe S, De Silva D, Samarasinghe D, Irugalbandara S. Arterial tortuosity syndrome: A rare inherited form of connective tissue disorder with SLR2A10 gene mutation. Sri Lanka Journal of Child Health. 2022;51(1):142–5. DOI: http://doi.org/10.4038/sljch.v51i1.10023

Wijesinghe, S., De Silva, D., Samarasinghe, D., & Irugalbandara, S. (2022). Arterial tortuosity syndrome: A rare inherited form of connective tissue disorder with SLR2A10 gene mutation. Sri Lanka Journal of Child Health, 51(1), 142–145. DOI: http://doi.org/10.4038/sljch.v51i1.10023

1. Wijesinghe S, De Silva D, Samarasinghe D, Irugalbandara S. Arterial tortuosity syndrome: A rare inherited form of connective tissue disorder with SLR2A10 gene mutation. Sri Lanka Journal of Child Health. 2022;51(1):142-145. DOI: http://doi.org/10.4038/sljch.v51i1.10023

Wijesinghe S and others, ‘Arterial Tortuosity Syndrome: A Rare Inherited Form of Connective Tissue Disorder with SLR2A10 Gene Mutation’ (2022) 51 Sri Lanka Journal of Child Health 142 DOI: http://doi.org/10.4038/sljch.v51i1.10023

Wijesinghe, Sithija, Deepthi De Silva, Duminda Samarasinghe, and Sunethra Irugalbandara. 2022. “Arterial Tortuosity Syndrome: A Rare Inherited Form of Connective Tissue Disorder with SLR2A10 Gene Mutation”. Sri Lanka Journal of Child Health 51 (1): 142–45. DOI: http://doi.org/10.4038/sljch.v51i1.10023

Wijesinghe, Sithija, Deepthi De Silva, Duminda Samarasinghe, and Sunethra Irugalbandara. “Arterial Tortuosity Syndrome: A Rare Inherited Form of Connective Tissue Disorder with SLR2A10 Gene Mutation”. Sri Lanka Journal of Child Health 51, no. 1 (2022): 142–45. DOI: http://doi.org/10.4038/sljch.v51i1.10023

Wijesinghe, S, et al.. “Arterial tortuosity syndrome: A rare inherited form of connective tissue disorder with SLR2A10 gene mutation”. Sri Lanka Journal of Child Health, vol. 51, no. 1, 2022, pp. 142–45. DOI: http://doi.org/10.4038/sljch.v51i1.10023