Wichajarn, Khunton, Thailand

• Vol 97, No 10: OCTOBER 2014 (SUPPL. 10) - Original Article
  Difference of Clinical Phenotypes and Immunological Features of 22q11.2 Deletion Syndrome in North-Eastern Thai Children Compare to Western Countries
  Abstract  PDF
• Vol 97, No 10: OCTOBER 2014 (SUPPL. 10) - Original Article
  Prevalence and Type of Associated Syndromes in Patients with Cleft Lip and Cleft Palate Who Received the Treatment in Tawanchai Center until 4-5 Years of Age
  Abstract  PDF
• Vol 99, No 8: AUGUST 2016 (SUPPL 5) - Case Report
  Iliac Artery Aneurysms in Menkes Disease: A Case Report
  Abstract  PDF
• Vol 99, No 8: AUGUST 2016 (SUPPL 5) - Special Article
  Birth Prevalence of Chromosome 22q11.2 Deletion Syndrome: A Systematic Review of Population-Based Studies
  Abstract  PDF
• Vol 99, No 8: AUGUST 2016 (SUPPL 5) - Special Article
  Assessment of Chromosome 22q11.2 Deletion in Patients with Isolated Cleft Palate: A Systematic Review of Prospective Studies
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• Vol 100, No 8: AUGUST 2017 (SUPPL 6) - Special Article
  Maternal Tobacco Smoke Exposure during Pregnancy and the Occurrence of Orofacial Clefts: A Systematic Review of Reported Meta-analyses
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• Vol 100, No 8: AUGUST 2017 (SUPPL 6) - Special Article
  Birth Prevalence of Goldenhar Syndrome (Severe Oculo-Auriculo-Vertebral Spectrum): A Systematic Review of Prospective Studies
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• Vol 100, No 8: AUGUST 2017 (SUPPL 6) - Special Article
  Cardiovascular Malformations in Patients with Oculo-Auriculo-Vertebral Spectrum: A Systematic Review
  Abstract  PDF
• Vol 101, No 5: MAY 2018 (SUPPL. 5) - Special Article
  Cardiovascular Malformations in Patients with Treacher Collins Syndrome: A Systematic Review
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• Vol 101, No 5: MAY 2018 (SUPPL. 5) - Special Article
  Gastrointestinal Malformations in Patients with Treacher Collins Syndrome: A Systematic Review
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• Vol 101, No 5: MAY 2018 (SUPPL. 5) - Special Article
  Urinary System Malformations in Patients with Treacher Collins syndrome: A Systematic Review
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• Vol 102, No 6: JUNE 2019 (SUPPL. 5) - Original Article
  Detection of the G1138A mutation in the FGFR3 gene for the diagnosis of achondroplasia by allele-specific polymerase chain reaction
  Abstract  PDF
• Vol 102, No 6: JUNE 2019 (SUPPL. 5) - Special Article
  PHACE syndrome: A review of clinical manifestation and management
  Abstract  PDF