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Biomedical Reports|August 8, 2025
Evaluation of common genetic risk factors for differentiated thyroid cancer in the Thai populationPatra Yeetong, Aunchalee Laipiriyakun, Jiraporn Sriprapaporn, et al.
Neurology. Genetics|December 2, 2022
Neurodevelopmental Disorder, Obesity, Pancytopenia, Diabetes Mellitus, Cirrhosis, and Renal Failure in ACBD6-Associated Syndrome: A Case ReportPatra Yeetong, Natthaporn Tanpowpong, Supphakorn Rakwongkhachon, et al.
Skeletal Radiology|May 11, 2018
Widespread and debilitating hemangiomas in a patient with enchondromatosis and D-2-hydroxyglutaric aciduriaPatra Yeetong, Teerasak Phewplung, Wuttichart Kamolvisit, et al.
Fertility and Sterility|March 4, 2008
Identification of mutations in the SRD5A2 gene in Thai patients with male pseudohermaphroditismTaninee Sahakitrungruang, Suttipong Wacharasindhu, Patra Yeetong, et al.
Dermatology (Basel, Switzerland)|June 6, 2015
A Frameshift Mutation in PEN-2 Causes Familial Comedones SyndromeWipa Panmontha, Pawinee Rerknimitr, Patra Yeetong, et al.
American Journal of Medical Genetics. Part A|October 21, 2009
Three novel mutations of the IRF6 gene with one associated with an unusual feature in Van der Woude syndromePatra Yeetong, Charan Mahatumarat, Pichit Siriwan, et al.
BMC Endocrine Disorders|June 19, 2016
Splicing analysis of CYP11B1 mutation in a family affected with 11β-hydroxylase deficiency: case reportPattaranatcha Charnwichai, Patra Yeetong, Kanya Suphapeetiporn, et al.
Gene|March 28, 2012
Two novel CTNS mutations in cystinosis patients in ThailandPatra Yeetong, Siraprapa Tongkobpetch, Pornchai Kingwatanakul, et al.
Brain : a Journal of Neurology|September 21, 2019
TTTCA repeat insertions in an intron of YEATS2 in benign adult familial myoclonic epilepsy type 4Patra Yeetong, Monnat Pongpanich, Chalurmpon Srichomthong, et al.
European Journal of Human Genetics : EJHG|September 25, 2020
Founder effect of the TTTCA repeat insertions in SAMD12 causing BAFME1Patra Yeetong, Chaipat Chunharas, Monnat Pongpanich, et al.
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