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The Southeast Asian Journal of Tropical Medicine and Public Health|May 27, 2005
Prenatal exclusion of Crouzon syndrome by mutation analysis of FGFR2Vorapong Phupong, Chalurmpon Srichomthong, Vorasuk ShotelersukAmerican Journal of Medical Genetics. Part A|August 1, 2018
Cole-Carpenter syndrome in a patient from ThailandThantrira Porntaveetus, Thanakorn Theerapanon, Chalurmpon Srichomthong, et al.Human Genome Variation|April 16, 2016
A novel PCCB mutation in a Thai patient with propionic acidemia identified by exome sequencingThantrira Porntaveetus, Chalurmpon Srichomthong, Kanya Suphapeetiporn, et al.Plos One|August 5, 2025
A comparison of DNA methylation detection between HiFi sequencing and whole genome bisulfite sequencing in monozygotic twins with Down syndromeKanyanee Promsawan, Chalurmpon Srichomthong, Monnat Pongpanich, et al.American Journal of Medical Genetics. Part A|August 2, 2017
Monoallelic FGFR3 and Biallelic ALPL mutations in a Thai girl with hypochondroplasia and hypophosphatasiaThantrira Porntaveetus, Chalurmpon Srichomthong, Kanya Suphapeetiporn, et al.International Journal of Molecular Medicine|November 13, 2003
A novel termination codon mutation of the WAS gene in a Thai family with Wiskott-Aldrich syndromePantipa Chatchatee, Chalurmpon Srichomthong, Auyporn Chewatavorn, et al.Journal of Human Genetics|June 27, 2014
ZRS 406A>G mutation in patients with tibial hypoplasia, polydactyly and triphalangeal first fingersPhatchara Norbnop, Chalurmpon Srichomthong, Kanya Suphapeetiporn, et al.International Journal of Molecular Medicine|March 13, 2003
A novel mutation, 1234del(C), of the IRF6 in a Thai family with Van der Woude syndromeVorasuk Shotelersuk, Chalurmpon Srichomthong, Koh-ichiro Yoshiura, et al.Genetics Research|November 21, 2013
FOXE1 mutations in Thai patients with oral cleftsChalurmpon Srichomthong, Rungnapa Ittiwut, Pichit Siriwan, et al.BMC Medical Genetics|December 14, 2016
Short stature, platyspondyly, hip dysplasia, and retinal detachment: an atypical type II collagenopathy caused by a novel mutation in the C-propeptide region of COL2A1: a case reportApiruk Sangsin, Chalurmpon Srichomthong, Monnat Pongpanich, et al.Pageof 6