Hui B. Chew
Kuala Lumpur, Malaysia
Last Updated: 09/26/2026
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Found 8 publications
Abstracts of the 36th World Congress on Ultrasound in Obstetrics and Gynecology, 4-7 September 2026, London, UK.
Journal: Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology
Published: July 06, 2026
A Common CHAT Gene Mutation of Congenital Myasthenic Syndrome Found in Kadazandusun Children.
Journal: Journal of pediatric genetics
Published: November 07, 2021
Mutation-specific pathophysiological mechanisms define different neurodevelopmental disorders associated with SATB1 dysfunction.
Journal: American journal of human genetics
Published: October 19, 2020
Progressive myoclonus epilepsies-Residual unsolved cases have marked genetic heterogeneity including dolichol-dependent protein glycosylation pathway genes.
Journal: American journal of human genetics
Published: June 29, 2020
RANBP2 susceptibility to infection-induced encephalopathy: Clinicoradiologic and molecular description in a Malaysian family.
Journal: Molecular genetics and metabolism reports
Published: March 26, 2020
Clinical, biochemical and genetic profiles of patients with mucopolysaccharidosis type IVA (Morquio A syndrome) in Malaysia: the first national natural history cohort study.
Journal: Orphanet journal of rare diseases
Published: March 16, 2019
Case report of treatment experience with idursulfase beta (Hunterase) in an adolescent patient with MPS II.
Journal: Molecular genetics and metabolism reports
Published: March 14, 2017
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Last Updated: 09/26/2026