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  • Sawitree Rattanasopha, Siraprapa Tongkobpetch, Chalurmpon Srichomthong, Pichit Siriwan, Kanya Suphapeetiporn, Vorasuk Shotelersuk
  • Biology, Medicine
  • European Journal of Human Genetics
  • 2012 (First Published: 1 October 2012)
  • Isolated cleft palate (CP) is common in humans and has complex genetic etiologies. Many genes have been found to contribute to CP, but the full spectrum of genes remains unknown. PCR-sequencing ofContinue Reading
  • Siraprapa Tongkobpetch, Kanya Suphapeetiporn, Pichit Siriwan, Vorasuk Shotelersuk
  • Medicine
  • International journal of oral and maxillofacial…
  • 2008 (First Published: 1 June 2008)
  • Non-syndromic cleft lip with or without cleft palate (CL/P) has a complex etiology with several genetic and environmental factors playing a role. The poliovirus receptor related-1 gene (PVRL1) hasContinue Reading
  • Kanya Suphapeetiporn, Pradermchai Kongkam, Jarturon Tantivatana, Thivaratana Sinthuwiwat, Siraprapa Tongkobpetch, Vorasuk Shotelersuk
  • Biology, Medicine
  • Japanese journal of clinical oncology
  • 2006 (First Published: 1 December 2006)
  • Bannayan-Riley-Ruvalcaba syndrome (BRRS) is an autosomal dominant disorder characterized by macrocephaly, intestinal hamartomatous polyps, lipomas and pigmented macules of the glans penis. WeContinue Reading
  • Petcharat Leoyklang, Kanya Suphapeetiporn, +7 authors Vorasuk Shotelersuk
  • Biology, Medicine
  • Human Genetics
  • 2013 (First Published: 1 December 2013)
  • Two syndromic cognitive impairment disorders have very similar craniofacial dysmorphisms. One is caused by mutations of SATB2, a transcription regulator and the other by heterozygous mutationsContinue Reading
  • Pramuk Amarinthnukrowh, Siraprapa Tongkobpetch, Apichai Kongpatanayothin, Kanya Suphapeetiporn, Vorasuk Shotelersuk
  • Biology, Medicine
  • Genetic testing and molecular biomarkers
  • 2010 (First Published: 1 December 2010)
  • AIM to describe genetic features of five unrelated Thai families with infantile-onset Pompe disease caused by mutations in the acid α-glucosidase (GAA) gene. METHODS total RNA and genomic DNA wereContinue Reading