W. Yeung

发表

Inherited metabolic diseases in the Southern Chinese population; Diseases Spectrum and estimated incidence from recurrent mutations

Josephine S. C. Chong, N. Tang, T. Fok, 2016 .

Inherited metabolic diseases in the Southern Chinese population: spectrum of diseases and estimated incidence from recurrent mutations.

Josephine S. C. Chong, Chi-kong Li, T. Fok, 2014, Pathology.

A common PRRT2 mutation in familial paroxysmal kinesigenic dyskinesia in Hong Kong: a case series of 16 patients.

C. Lam, Y. Yuen, C. Law, 2016, Hong Kong medical journal = Xianggang yi xue za zhi.

A Case of Poliomyelitis-like Syndrome

W. Yeung, E. Fung, T. Lam, 2007 .

An infant with encephalitis

M. Ip, T. Fok, W. Yeung, 1997, The Lancet.

Whole-exome sequencing of a quartet family identifies DTYMK mutations in siblings with mitochondrial DNA depletion syndrome.

C. Lam, C. Law, Ka-chung Wong, 2019, Clinica chimica acta; international journal of clinical chemistry.

Spectrum of mutations in the MECP2 gene in patients with infantile autism and Rett syndrome

V. Wong, C. Pang, T. Fok, 2000, Journal of medical genetics.

Recurrent and novel mutations of GCDH gene in Chinese glutaric acidemia type I families

T. Fok, A. Chan, N. Tang, 2000, Human mutation.

patients with infantile autism and Rett syndrome gene in MECP2 Spectrum of mutations in the

V. Wong, C. Pang, C. Lam, 2006 .

Biochemical and molecular characterization of tyrosine hydroxylase deficiency in Hong Kong Chinese.

V. Wong, S. Tam, C. Fung, 2010, Molecular genetics and metabolism.

Red eyes as the initial presentation of systemic meningococcal infection

K. Yam, W. Chan, W. Yeung, 2003, Journal of paediatrics and child health.

A Chinese girl with Leigh syndrome: Effect of botulinum toxin on dystonia

W. Yeung, K. Goh, Tf Leung, 1998, Journal of paediatrics and child health.