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List of works by Rachaneekorn Tammachote

A common and two novel GBA mutations in Thai patients with Gaucher disease ⬇️

scientific article published on May 30, 2013

Ciliary and centrosomal defects associated with mutation and depletion of the Meckel syndrome genes MKS1 and MKS3

scientific article

Epitope-tagged Pkhd1 tracks the processing, secretion, and localization of fibrocystin.

scientific article published on 21 October 2011

Glucocorticoid receptor gene (NR3C1) promoter is hypermethylated in Thai females with major depressive disorder.

scientific article published on 29 December 2015

Prenatal diagnosis of a novel mutation, c.529C>T (p.Q177X), in the BCKDHA gene in a family with maple syrup urine disease.

scientific article published on 24 February 2009

Primary hyperoxaluria type 1 and brachydactyly mental retardation syndrome caused by a novel mutation in AGXT and a terminal deletion of chromosome 2

scientific article published on 20 July 2012

The Utilization of Karyotyping, iFISH, and MLPA for the Detection of Recurrence Genetic Aberrations in Multiple Myeloma

scientific article published on 26 November 2017

and polymorphisms are associated with osteoporosis in Thai patients

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