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Hui Bein Chew
Hui Bein Chew
Hospital Kuala Lumpur
Internal medicine
Medicine
Genetics
Respiratory failure
Age of onset
5
Papers
7
Citations
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Foetal 2:1 atrioventricular block in a patient with Timothy syndrome (LQT8) (RCDD code: VI‐1B‐1.2)
2019
Journal of Rare Cardiovascular Diseases
Putri Yubbu
Hui Bein Chew
Yusnita Yakob
Seok Hian Lua
Hasri Samion
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Analysis of the tissue-nonspecific alkaline phosphatase mutations in Malaysian patients with hypophosphatasia
2017
Hideo Orimo
Atsushi Watanabe
Satomi Saito
Tomohiro Matsumura
Shiho Saito
Motoko Sasaki
Takashi Okada
Bee Chin Chen
Hui Bein Chew
Wee Teik Keng
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Case report of treatment experience with idursulfase beta (Hunterase) in an adolescent patient with MPS II
2017
Molecular genetics and metabolism reports
Lock Hock Ngu
Winnie Ong Peitee
Huey Yin Leong
Hui Bein Chew
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Citations (6)
AB168. Novel DYM compound heterozygous mutations in a Malaysian boy with Dyggve-Melchior-Clausen syndrome
2015
Annals of Translational Medicine
Winnie Peitee Ong
Muzhirah Haniffa
Huey Yin Leong
Hui Bein Chew
Gaik Siew Ch’ng
Lock Hock Ngu
Nisha Patel
Mais Hashem
Fowzan S. Alkuraya
Wee Teik Keng
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AB085. Imprinting mutation of CDKN1C in Beckwith-Wiedemann Syndrome: inheritance, genetic counselling and surveillance
2015
Annals of Translational Medicine
Hui Bein Chew
Winnie Peitee Ong
Muzhirah Haniffa
Huey Yin Leong
Thurga Krishnan
R. Poh
M.K. Thong
Mohd Taufik Ishak
Wee Teik Keng
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