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Clinical and Experimental Dermatology|June 15, 2005
Two novel frameshift mutations of the EBP gene in two unrelated Thai girls with Conradi-Hünermann-Happle syndromeV Shotelersuk, S TongkobpetchMolecular Genetics and Metabolism|October 27, 1998
Hermansky-Pudlak syndrome: models for intracellular vesicle formationV Shotelersuk, W A GahlJIMD Reports|November 22, 2017
Severe Hyperammonemic Encephalopathy Requiring Dialysis Aggravated by Prolonged Fasting and Intermittent High Fat Load in a Ramadan Fasting Month in a Patient with CPTII Homozygous MutationP Phowthongkum, C Ittiwut, V ShotelersukJournal of Medical Genetics|June 3, 2006
A mutation of the p63 gene in non-syndromic cleft lipP Leoyklang, P Siriwan, V ShotelersukJournal of Medical Genetics|July 5, 2005
Significant association between IRF6 820G->A and non-syndromic cleft lip with or without cleft palate in the Thai populationC Srichomthong, P Siriwan, V ShotelersukHuman Mutation|November 26, 1999
CTNS mutations in patients with cystinosisY Anikster, V Shotelersuk, W A GahlJournal of the Medical Association of Thailand = Chotmaihet Thangphaet|February 24, 2001
A Thai boy with hereditary enzymopenic methemoglobinemia type IIV Shotelersuk, P Tosukhowong, P Chotivitayatarakorn, et al.Clinical and Experimental Dermatology|April 6, 2005
De novo missense mutation, S541Y, in the p63 gene underlying Rapp-Hodgkin ectodermal dysplasia syndromeV Shotelersuk, S Janklat, P Siriwan, et al.Clinical Dysmorphology|January 11, 2001
An Asian girl with a 'milder' form of the Hydrolethalus syndromeV Shotelersuk, V Punyavoravud, S Phudhichareonrat, et al.Clinical Genetics|September 18, 2007
TBX22 mutations are a frequent cause of non-syndromic cleft palate in the Thai populationK Suphapeetiporn, S Tongkobpetch, P Siriwan, et al.Pageof 5