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	1.	A different spectrum of DMD gene mutations in local Chinese patients with Duchenne/Becker muscular dystrophy. [electronic resource] by Lo, Ivan Fai-man Lai, Kent Keung-san Tong, Tony Ming-for Lam, Stephen Tak-sum Producer: 20060809 In: Chinese medical journal vol. 119 Availability: No items available. Save to lists Add to cart (remove)
	2.	Performance of chromosomal microarray for patients with intellectual disabilities/developmental delay, autism, and multiple congenital anomalies in a Chinese cohort. [electronic resource] by Chong, Wilson Wai Sing Lo, Ivan Fai Man Lam, Stephen Tak Sum Wang, Chi Chiu Luk, Ho Ming Leung, Tak Yeung Choy, Kwong Wai Producer: 20140613 In: Molecular cytogenetics vol. 7 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Delayed diagnosis of 22q11.2 deletion syndrome in an adult Chinese lady. [electronic resource] by Shea, Yat-Fung Lee, Chi-Ho Gill, Harinder Chow, Wing-Sun Lam, Yui-Ming Luk, Ho-Ming Lam, Stephen Tak-Sum Chu, Leung-Wing Producer: 20130213 In: Chinese medical journal vol. 125 Availability: No items available. Save to lists Add to cart (remove)
	4.	Identification of novel FBN1 and TGFBR2 mutations in 65 probands with Marfan syndrome or Marfan-like phenotypes. [electronic resource] by Chung, Brian Hon-Yin Lam, Stephen Tak-Sum Tong, Tony Ming-For Li, Susanna Yuk-Han Lun, Kin-Shing Chan, Daniel Hon-Chuen Fok, Susanna Fung-Shan Or, June Siu-Fong Smith, David Keith Yang, Wanling Lau, Yu-Lung Producer: 20090923 In: American journal of medical genetics. Part A vol. 149A Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)