Susanna Li

Identification of novel FBN1 and TGFBR2 mutations in 65 probands with Marfan syndrome or Marfan‐like phenotypes

Y. Lau, S. Lam, B. Chung, 2009, American journal of medical genetics. Part A.

Rett Syndrome: Prevalence Among Chinese and a Comparison of MECP2 Mutations of Classic Rett Syndrome With Other Neurodevelopmental Disorders

V. Wong, Susanna Li, 2007, Journal of child neurology.

Exon 3 polymorphisms of dopamine D4 receptor (DRD4) gene and attention deficit hyperactivity disorder in Chinese children

V. Wong, D. Cheuk, Susanna Li, 2006, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

No association between VNTR polymorphisms of dopamine transporter gene and attention deficit hyperactivity disorder in Chinese children

V. Wong, Virginia Wong, D. Cheuk, 2006, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Mutation of gene in spinal muscular atrophy respiratory distress type I.

V. Wong, B. Chung, S. L. Lee, 2006, Pediatric neurology.