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Pornprot Limprasert

Showing results (11-20 of 38) with videos related to

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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.
Scientific Reports|November 1, 2024
Prevalence and implications of fragile X premutation screening in ThailandAreerat Hnoonual, Sunita Kaewfai, Chanin Limwongse, et al.
Genetics Research International|April 5, 2016
Unique AGG Interruption in the CGG Repeats of the FMR1 Gene Exclusively Found in Asians Linked to a Specific SNP HaplotypePornprot Limprasert, Janpen Thanakitgosate, Kanoot Jaruthamsophon, et al.
European Journal of Medical Genetics|July 7, 2007
Mutation screening of the Aristaless-related homeobox (ARX) gene in Thai pediatric patients with delayed development: first report from ThailandSinitdhorn Rujirabanjerd, Kobkul Tongsippunyoo, Thanya Sripo, 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.
Medicine|September 9, 2020
Significant associations between 5-hydroxytryptaminetransporter-linked promoter region polymorphisms of the serotonin transporter (solute carrier family 6 member 4) gene and Thai patients with autism spectrum disorderWikrom Wongpaiboonwattana, Oradawan Plong-On, Areerat Hnoonual, et al.
Scientific Reports|March 31, 2017
HLA-B*15:21 and carbamazepine-induced Stevens-Johnson syndrome: pooled-data and in silico analysisKanoot Jaruthamsophon, Varomyalin Tipmanee, Antida Sangiemchoey, et al.
Journal of the Medical Association of Thailand = Chotmaihet Thangphaet|December 19, 2014
A new structured interview for children with autism spectrum disorder based on the DSM-IVTippawan Hansakunachai, Rawiwan Roongpraiwan, Tasnawat Sombuntham, et al.
The Journal of Molecular Diagnostics : JMD|October 30, 2025
Clinical Utility and Performance of Methylation-Specific Triplet-Primed PCR for Fragile X Syndrome DiagnosisAreerat Hnoonual, Wipawan Arunthong, Oradawan Plong-On, 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.
Pageof 4

Showing results (11-20 of 38) with videos related to

Sort By:
Pageof 4
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.
Scientific Reports|November 1, 2024
Prevalence and implications of fragile X premutation screening in ThailandAreerat Hnoonual, Sunita Kaewfai, Chanin Limwongse, et al.
Genetics Research International|April 5, 2016
Unique AGG Interruption in the CGG Repeats of the FMR1 Gene Exclusively Found in Asians Linked to a Specific SNP HaplotypePornprot Limprasert, Janpen Thanakitgosate, Kanoot Jaruthamsophon, et al.
European Journal of Medical Genetics|July 7, 2007
Mutation screening of the Aristaless-related homeobox (ARX) gene in Thai pediatric patients with delayed development: first report from ThailandSinitdhorn Rujirabanjerd, Kobkul Tongsippunyoo, Thanya Sripo, 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.
Medicine|September 9, 2020
Significant associations between 5-hydroxytryptaminetransporter-linked promoter region polymorphisms of the serotonin transporter (solute carrier family 6 member 4) gene and Thai patients with autism spectrum disorderWikrom Wongpaiboonwattana, Oradawan Plong-On, Areerat Hnoonual, et al.
Scientific Reports|March 31, 2017
HLA-B*15:21 and carbamazepine-induced Stevens-Johnson syndrome: pooled-data and in silico analysisKanoot Jaruthamsophon, Varomyalin Tipmanee, Antida Sangiemchoey, et al.
Journal of the Medical Association of Thailand = Chotmaihet Thangphaet|December 19, 2014
A new structured interview for children with autism spectrum disorder based on the DSM-IVTippawan Hansakunachai, Rawiwan Roongpraiwan, Tasnawat Sombuntham, et al.
The Journal of Molecular Diagnostics : JMD|October 30, 2025
Clinical Utility and Performance of Methylation-Specific Triplet-Primed PCR for Fragile X Syndrome DiagnosisAreerat Hnoonual, Wipawan Arunthong, Oradawan Plong-On, 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.
Pageof 4