AB083. Social media with cartoon characters as a powerful tool for expanding medical education and raising awareness of rare genetic diseases

Gelijkaardige items

• AB085. Diagnosis of Prader-Willi syndrome using computer-aided facial dysmorphism analysis in Thai patients
  door: Tim-Aroon, Thipwimol, et al.
  Gepubliceerd in: (2017)
• A novel TCN2 mutation with unusual clinical manifestations of hemolytic crisis and unexplained metabolic acidosis: expanding the genotype and phenotype of transcobalamin II deficiency
  door: Pongpak Pongphitcha, et al.
  Gepubliceerd in: (2022-04-01)
• Correction to: Perspectives of adults with Klinefelter syndrome, unaffected adolescent males, and parents of affected children toward diagnosis disclosure: a Thai experience
  door: Suwannachat, Sukrit, et al.
  Gepubliceerd in: (2019)
• Perspectives of adults with Klinefelter syndrome, unaffected adolescent males, and parents of affected children toward diagnosis disclosure: a Thai experience
  door: Suwannachat, Sukrit, et al.
  Gepubliceerd in: (2019)
• Growth charts for Thai children with Prader-Willi syndrome aged 0–18 years
  door: Mongkollarp, Nantiya, et al.
  Gepubliceerd in: (2020)