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	1.	Chinese patients with p.Ala172Phe-related Pfeiffer syndrome: a case and literature review. [electronic resource] by Cheng, Shirley Sze Wing Lo, Ivan Fai-Man Luk, Ho-Ming Producer: 20181017 In: Clinical dysmorphology vol. 27 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Myhre syndrome: a report of six Chinese patients and literature review. [electronic resource] by Yu, Kris Pui-Tak Luk, Ho-Ming Chung, Brian Hon-Yin Lo, Ivan Fai-Man Producer: 20191206 In: Clinical dysmorphology vol. 28 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	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)
	4.	A PTPN11 allele encoding a catalytically impaired SHP2 protein in a patient with a Noonan syndrome phenotype. [electronic resource] by Edwards, Jonathan J Martinelli, Simone Pannone, Luca Lo, Ivan Fai-Man Shi, Lisong Edelmann, Lisa Tartaglia, Marco Luk, Ho-Ming Gelb, Bruce D Producer: 20150420 In: American journal of medical genetics. Part A vol. 164A Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	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)
	6.	A report of three families with FBN1-related acromelic dysplasias and review of literature for genotype-phenotype correlation in geleophysic dysplasia. [electronic resource] by Cheng, S W Luk, Ho-Ming Chu, YoYo W Y Tung, Yuet-Ling Kwan, Elanie Yin-Wah Lo, Ivan Fai-Man Chung, Brian Hon-Yin Producer: 20180827 In: European journal of medical genetics vol. 61 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	Identification of a PTEN mutation with reduced protein stability, phosphatase activity, and nuclear localization in Hong Kong patients with autistic features, neurodevelopmental delays, and macrocephaly. [electronic resource] by Wong, Chi Wai Or, Penelope Mei Yu Wang, Yubing Li, Lisha Li, Jing Yan, Mingfei Cao, Ye Luk, Ho Ming Tong, Tony Ming For Leslie, Nick R Lo, Ivan Fai-Man Choy, Kwong Wai Chan, Andrew Man Lok Producer: 20190911 In: Autism research : official journal of the International Society for Autism Research vol. 11 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)