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Current Opinion in Pediatrics|September 19, 2017
Medical genetic services in a developing country: lesson from ThailandChanin Limwongse
Journal of the Medical Association of Thailand = Chotmaihet Thangphaet|November 30, 2006
Real-time three dimensional sonographic features of an early third trimester fetus with achondrogenesisTuangsit Wataganara, Anuwat Sutanthavibool, Chanin Limwongse
Journal of the Medical Association of Thailand = Chotmaihet Thangphaet|December 8, 2015
Liddle's Syndrome: A Case ReportMeta Phoojaroenchanachai, Peera Buranakitjaroen, Chanin Limwongse
Journal of Stroke and Cerebrovascular Diseases : the Official Journal of National Stroke Association|May 18, 2020
Incidence and risk factors of vascular dementia in Thai stroke patientsPornpatr A Dharmasaroja, Chanin Limwongse, Thammanard Charernboon
Scientific Reports|November 1, 2024
Prevalence and implications of fragile X premutation screening in ThailandAreerat Hnoonual, Sunita Kaewfai, Chanin Limwongse, et al.
Prenatal Diagnosis|March 26, 2005
Ectrodactyly-ectodermal dysplasia-clefting (EEC) syndrome presenting with a large nephrogenic cyst, severe oligohydramnios and hydrops fetalis: a case report and review of the literatureTuenjai Chuangsuwanich, Prasert Sunsaneevithayakul, Kobkun Muangsomboon, et al.
Journal of the Medical Association of Thailand = Chotmaihet Thangphaet|July 16, 2003
Ultrasonographic prenatal diagnosis of Treacher Collins syndrome: a case reportPornpimol Ruangvutilert, Anuwat Sutantawibul, Prasert Sunsaneevithayakul, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|April 7, 2009
A novel mutation in the beta-subunit of the epithelial sodium channel gene (SCNN1B) in a Thai family with Liddle's syndromePairunyar Sawathiparnich, Achra Sumboonnanonda, Praewvarin Weerakulwattana, et al.
European Journal of Medical Genetics|July 17, 2012
Polyglutamined expanded androgen receptor interacts with chaperonin CCTSuttikarn Pongtepaditep, Thawornchai Limjindaporn, Patcharee Lertrit, et al.
Journal of the Medical Association of Thailand = Chotmaihet Thangphaet|April 6, 2006
Floppy infant caused by MTM1 mutation: a first genetically-confirmed X-linked myotubular myopathy patient in ThailandTeerin Liewluck, Natte Raksadawan, Chanin Limwongse, et al.
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