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2. Characteristics of β‐secretase activity on APP‐V604M and APP‐V669L. (20th December 2022)

4. Identification of novel mutation in RANKL by whole‐exome sequencing in a Thai family with osteopetrosis; a case report and review of RANKL osteopetrosis. Issue 7 (30th May 2021)

9. Skewed X chromosome inactivation in girls and female adolescents with autoimmune thyroid disease. (17th October 2018)

10. Small Ancestry Informative Marker panels for complete classification between the original four HapMap populations. (14th November 2012)