Tzer H. Ting
Kuala Selangor, Malaysia
Last Updated: 09/26/2026
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Found 12 publications
Identification of a Novel IGSF1 Variant in Two Malaysian Male Siblings with Central Hypothyroidism and Macroorchidism
Journal: Journal of clinical research in pediatric endocrinology
Published: April 22, 2024
Diagnosis of an intermediate case of maple syrup urine disease: A case report.
Journal: World journal of clinical cases
Published: September 20, 2022
Features of BSCL2 related congenital generalized lipodystrophy in China: long-term follow-up of three patients and literature review.
Journal: Journal of pediatric endocrinology & metabolism : JPEM
Published: July 27, 2022
Whole exome sequencing identifies two novel variants in PHEX and DMP1 in Malaysian children with hypophosphatemic rickets.
Journal: Italian journal of pediatrics
Published: June 27, 2022
Features of chinese patients with sitosterolemia.
Journal: Lipids in health and disease
Published: November 14, 2021
Genetic basis of hereditary hypophosphataemic rickets and phenotype presentation in children and adults.
Journal: Endokrynologia Polska
Published: January 18, 2021
Molecular and clinical characteristics of monogenic diabetes mellitus in southern Chinese children with onset before 3 years of age.
Journal: BMJ open diabetes research & care
Published: March 10, 2020
Molecular diagnosis of maturity-onset diabetes of the young in a cohort of Chinese children.
Journal: Pediatric diabetes
Published: June 04, 2019
Vitamin-D-deficiency rickets even with abundant sunlight -A case to highlight emerging problem.
Journal: The Medical journal of Malaysia
Published: January 15, 2017
Clinical and Mutational Features of Three Chinese Children with Congenital Generalized Lipodystrophy.
Journal: Journal of clinical research in pediatric endocrinology
Published: September 10, 2016
Showing 1-12 of 12
Last Updated: 09/26/2026