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Journal of the Medical Association of Thailand = Chotmaihet Thangphaet|January 13, 2006
Multiplex methylation specific PCR analysis of fragile X syndrome: experience in Songklanagarind HospitalChariyawan Charalsawadi, Thanya Sripo, Pornprot Limprasert
Plos One|November 5, 2016
Maternal Age-Specific Rates for Trisomy 21 and Common Autosomal Trisomies in Fetuses from a Single Diagnostic Center in ThailandKanoot Jaruthamsophon, Hutcha Sriplung, Chariyawan Charalsawadi, et al.
Genetics Research International|November 9, 2016
Screening for Subtelomeric Rearrangements in Thai Patients with Intellectual Disabilities Using FISH and Review of Literature on Subtelomeric FISH in 15,591 Cases with Intellectual DisabilitiesChariyawan Charalsawadi, Jariya Khayman, Verayuth Praphanphoj, et al.
American Journal of Medical Genetics. Part A|November 22, 2014
Mosaicism for trisomy 21: a reviewPaulie Papavassiliou, Chariyawan Charalsawadi, Kelly Rafferty, et al.
Frontiers in Genetics|October 11, 2021
Case Report: An Atypical Angelman Syndrome Case With Obesity and Fulfilled Autism Spectrum Disorder Identified by MicroarrayAreerat Hnoonual, Phawin Kor-Anantakul, Chariyawan Charalsawadi, et al.
International Journal of Molecular Sciences|August 14, 2025
A 30-Year Experience in Fragile X Syndrome Molecular Diagnosis from a Laboratory in ThailandAreerat Hnoonual, Oradawan Plong-On, Duangkamol Tangviriyapaiboon, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|December 24, 2023
Clinical and molecular characteristics of FMR1 microdeletion in patient with fragile X syndrome and review of the literatureAreerat Hnoonual, Oradawan Plong-On, Juthamas Worachotekamjorn, et al.
International Journal of Pediatrics|July 29, 2017
Common Clinical Characteristics and Rare Medical Problems of Fragile X Syndrome in Thai Patients and Review of the LiteratureChariyawan Charalsawadi, Juthamas Wirojanan, Somchit Jaruratanasirikul, et al.
Clinical and Translational Science|June 19, 2024
Molecular identification of HLA-B75 serotype markers by qPCR: A more inclusive pharmacogenetic approach before carbamazepine prescriptionKanoot Jaruthamsophon, Pornsiri Sangmanee, Oradawan Plong-On, et al.
International Journal of Pediatrics|December 27, 2021
No Evidence of Abnormal Expression of Beta-Catenin and Bcl-2 Proteins in Pilomatricoma as One Clinical Feature of Tetrasomy 9p SyndromeChariyawan Charalsawadi, Sasipong Trongnit, Kanoot Jaruthamsophon, et al.
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