Main Article Content

Abstract

No Abstract

Keywords

genetic counseling Indonesia rare disease prevention

Article Details

How to Cite
Rujito, L. (2018). Genetic Counseling in Indonesia as a Mandatory Service. JKKI : Jurnal Kedokteran Dan Kesehatan Indonesia, 9(1), 1–2. https://doi.org/10.20885/JKKI.Vol9.Iss1.art1

References

  1. Mester J, Schreiber A, Moran R. Genetic counselors: Your partners in clinical practice. Cleveland Clinic Journal of Medicine. 2012;79(8):560–8.
  2. Global Genes. RARE diseases: Facts and statistics [Internet]. 2017. Available from: https://globalgenes.org/rare-diseases-facts-statistics/
  3. Kementerian Kesehatan Republik Indonesia. Pencegahan thalassemia (Hasil kajian Health Technology Assesment tahun 2009). Jakarta; 2010.
  4. Parker SE, Mai CT, Canfield MA, Rickard R, Wang Y, Meyer RE, et al. Updated national birth prevalence estimates for selected birth defects in the United States, 2004–2006. Birth Defects Research Part A: Clinical and Molecular Teratology. 2010;88(12):1008–16.
  5. Alabek M, Mohan R, Raia M. Genetic counselling for hemophilia. 2015.
  6. Faradz S, Buckley M, Lam-Po-Tang, Leigh D, Holden J. Molecular screening for fragile X syndrome among Indonesian children with developmental disability. American Journal of Medical Genetics. 1999;83(4):350–1.
  7. Cao A, Kan YW. The prevention of thalassemia. Cold Spring Harbor Perspectives in Medicine. 2013;3(2):a011775.
  8. Rujito L, Ghozali PA. Initiating development of genetic counseling services in the health services unit: An initial assessment. Journal of the Indonesian Medical Association. 2011;60(2):426–30.