Patra Yeetong
Bangkok, Thailand
Last Updated: 09/26/2026
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Found 23 publications
Evaluation of common genetic risk factors for differentiated thyroid cancer in the Thai population.
Journal: Biomedical reports
Published: March 18, 2025
A missense variant in ASCL5 leads to lobodontia.
Journal: Nature communications
Published: October 26, 2024
Rare Variants Cause Charcot-Marie-Tooth Disease in Malian Families.
Journal: Brain and behavior
Published: September 19, 2024
Pentanucleotide Repeat Insertions in RAI1 Cause Benign Adult Familial Myoclonic Epilepsy Type 8.
Journal: Movement disorders : official journal of the Movement Disorder Society
Published: July 11, 2023
Long-read Nanopore sequencing identified D4Z4 contractions in patients with facioscapulohumeral muscular dystrophy.
Journal: Neuromuscular disorders : NMD
Published: January 16, 2023
Neurodevelopmental Disorder, Obesity, Pancytopenia, Diabetes Mellitus, Cirrhosis, and Renal Failure in ACBD6-Associated Syndrome: A Case Report.
Journal: Neurology. Genetics
Published: July 18, 2022
Bi-allelic ACBD6 variants lead to a neurodevelopmental syndrome with progressive and complex movement disorders.
Journal: Brain : a journal of neurology
Published: May 18, 2022
Long-read Amplicon Sequencing of the CYP21A2 in 48 Thai Patients With Steroid 21-Hydroxylase Deficiency.
Journal: The Journal of clinical endocrinology and metabolism
Published: September 21, 2021
Founder effect of the TTTCA repeat insertions in SAMD12 causing BAFME1.
Journal: European journal of human genetics : EJHG
Published: December 16, 2019
TTTCA repeat insertions in an intron of YEATS2 in benign adult familial myoclonic epilepsy type 4.
Journal: Brain : a journal of neurology
Published: February 26, 2019
Last Updated: 09/26/2026