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Pornprot Limprasert

Showing results (21-30 of 38) with videos related to

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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.
American Journal of Medical Genetics. Part A|January 20, 2007
De novo subtelomeric deletion of 15q associated with satellite translocation in a child with developmental delay and severe growth retardationSinitdhorn Rujirabanjerd, Warapong Suwannarat, Thanya Sripo, 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.
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.
Journal of the Medical Association of Thailand = Chotmaihet Thangphaet|November 25, 2004
Clinical abnormalities, intervention program, and school attendance of Down syndrome children in southern ThailandSomchit Jaruratanasirikul, Somkiat Soponthammarak, Prasin Chanvitan, et al.
Genetic Testing and Molecular Biomarkers|February 19, 2011
A new method for FMR1 gene methylation screening by multiplex methylation-specific real-time polymerase chain reactionMarjanu Hikmah Elias, Ravindran Ankathil, Abdul Razak Salmi, et al.
Frontiers in Genetics|December 5, 2022
Case report: Molecular analysis of a 47,XY,+21/46,XX chimera using SNP microarray and review of literatureChariyawan Charalsawadi, Somchit Jaruratanasirikul, Areerat Hnoonual, et al.
Disease Markers|December 27, 2016
Exome Sequencing Identifies Compound Heterozygous Mutations in <i>SCN5A</i> Associated with Congenital Complete Heart Block in the Thai PopulationChuphong Thongnak, Pornprot Limprasert, Duangkamol Tangviriyapaiboon, et al.
International Journal of Genomics|June 12, 2018
Whole-Exome Sequencing Identifies One De Novo Variant in the <i>FGD6</i> Gene in a Thai Family with Autism Spectrum DisorderChuphong Thongnak, Areerat Hnoonual, Duangkamol Tangviriyapaiboon, et al.
Pageof 4

Showing results (21-30 of 38) with videos related to

Sort By:
Pageof 4
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.
American Journal of Medical Genetics. Part A|January 20, 2007
De novo subtelomeric deletion of 15q associated with satellite translocation in a child with developmental delay and severe growth retardationSinitdhorn Rujirabanjerd, Warapong Suwannarat, Thanya Sripo, 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.
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.
Journal of the Medical Association of Thailand = Chotmaihet Thangphaet|November 25, 2004
Clinical abnormalities, intervention program, and school attendance of Down syndrome children in southern ThailandSomchit Jaruratanasirikul, Somkiat Soponthammarak, Prasin Chanvitan, et al.
Genetic Testing and Molecular Biomarkers|February 19, 2011
A new method for FMR1 gene methylation screening by multiplex methylation-specific real-time polymerase chain reactionMarjanu Hikmah Elias, Ravindran Ankathil, Abdul Razak Salmi, et al.
Frontiers in Genetics|December 5, 2022
Case report: Molecular analysis of a 47,XY,+21/46,XX chimera using SNP microarray and review of literatureChariyawan Charalsawadi, Somchit Jaruratanasirikul, Areerat Hnoonual, et al.
Disease Markers|December 27, 2016
Exome Sequencing Identifies Compound Heterozygous Mutations in <i>SCN5A</i> Associated with Congenital Complete Heart Block in the Thai PopulationChuphong Thongnak, Pornprot Limprasert, Duangkamol Tangviriyapaiboon, et al.
International Journal of Genomics|June 12, 2018
Whole-Exome Sequencing Identifies One De Novo Variant in the <i>FGD6</i> Gene in a Thai Family with Autism Spectrum DisorderChuphong Thongnak, Areerat Hnoonual, Duangkamol Tangviriyapaiboon, et al.
Pageof 4