1. A novel de novo mutation substantiates KDF1 as a gene causing ectodermal dysplasia. (14th May 2019) Authors: Manaspon, C.; Thaweesapphithak, S.; Osathanon, T.; Suphapeetiporn, K.; Porntaveetus, T.; Shotelersuk, V. Journal: British journal of dermatology Issue: Volume 181:Number 2(2019) Page Start: 419 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. A novel de novo mutation substantiates KDF1 as a gene causing ectodermal dysplasia. (1st August 2019) Authors: Manaspon, C.; Thaweesapphithak, S.; Osathanon, T.; Suphapeetiporn, K.; Porntaveetus, T.; Shotelersuk, V. Journal: British journal of dermatology Issue: Volume 181:Number 2(2019) Page Start: 419 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Clinical and genetic data of thai subjects with familial hypercholesterolemia from the Thai FH registry. (August 2022) Authors: Ganokroj, P.; Muanpetch, S.; Thongtang, N.; Krittayaphong, R.; Suphapeetiporn, K.; Shotelersuk, V.; Khovidhunkit, W. Journal: Atherosclerosis Issue: Volume 355(2022) Page Start: 175 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Clinical and Molecular Characterization of Thai Patients with Wiskott–Aldrich Syndrome. (26th December 2012) Authors: Amarinthnukrowh, P.; Ittiporn, S.; Tongkobpetch, S.; Chatchatee, P.; Sosothikul, D.; Shotelersuk, V.; Suphapeetiporn, K. Journal: Scandinavian journal of immunology Issue: Volume 77:Number 1(2013:Jan.) Page Start: 69 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Novel compound heterozygous mutations in KREMEN1 confirm it as a disease gene for ectodermal dysplasia. (13th June 2018) Authors: Intarak, N.; Theerapanon, T.; Srijunbarl, A.; Suphapeetiporn, K.; Porntaveetus, T.; Shotelersuk, V. Journal: British journal of dermatology Issue: Volume 179:Number 3(2018) Page Start: 758 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Novel compound heterozygous mutations in KREMEN1 confirm it as a disease gene for ectodermal dysplasia. (1st September 2018) Authors: Intarak, N.; Theerapanon, T.; Srijunbarl, A.; Suphapeetiporn, K.; Porntaveetus, T.; Shotelersuk, V. Journal: British journal of dermatology Issue: Volume 179:Number 3(2018) Page Start: 758 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗