Teck W. Ting
Singapore, Singapore
Last Updated: 09/26/2026
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Found 18 publications
Deep phenotyping of patients with citrin deficiency in Singapore- single centre experience.
Journal: Molecular genetics and metabolism
Published: February 25, 2025
National Thalassemia Registry: a 30 year journey of implementing carrier screening in Singapore.
Journal: The Lancet regional health. Western Pacific
Published: September 25, 2024
Author Correction: Analysis and visualisation of electronic health records data to identify undiagnosed patients with rare genetic diseases.
Journal: Scientific reports
Published: May 02, 2024
Cluster analysis and visualisation of electronic health records data to identify undiagnosed patients with rare genetic diseases.
Journal: Scientific reports
Published: November 01, 2023
MIRAGE Syndrome Caused by a De Novo c.3406G>C (p. Glu1136Gln) Mutation in the SAMD9 Gene Presenting With Neonatal Adrenal Insufficiency and Recurrent Intussusception: A Case Report.
Journal: Frontiers in endocrinology
Published: July 16, 2021
Singapore Undiagnosed Disease Program: Genomic Analysis aids Diagnosis and Clinical Management.
Journal: Archives of disease in childhood
Published: March 19, 2020
Genetic landscape of congenital disorders in patients from Southeast Asia: results from sequencing using a gene panel for Mendelian phenotypes.
Journal: Archives of disease in childhood
Published: March 17, 2020
Enzyme replacement therapy desensitization in a child with infantile onset Pompe disease.
Journal: Asian Pacific journal of allergy and immunology
Published: February 17, 2020
Identification of KMT2D and KDM6A variants by targeted sequencing from patients with Kabuki syndrome and other congenital disorders.
Journal: Gene
Published: November 28, 2019
Coffin-Siris Syndrome-1: Report of five cases from Asian populations with truncating mutations in the ARID1B gene.
Journal: Journal of the neurological sciences
Published: June 18, 2019
Further delineation of CDC45-related Meier-Gorlin syndrome with craniosynostosis and review of literature.
Journal: European journal of medical genetics
Published: September 25, 2018
The genotypic and phenotypic spectrum of MTO1 deficiency.
Journal: Molecular genetics and metabolism
Published: July 28, 2017
Last Updated: 09/26/2026