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Stephen T S Lam

Showing results (1-10 of 31) with videos related to

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Beijing Da Xue Xue Bao. Yi Xue Ban = Journal of Peking University. Health Sciences|March 7, 2006
Experience of medical genetics in Hong KongStephen T S Lam
Annals of the Academy of Medicine, Singapore|November 12, 2009
Issues on universal screening for galactosemiaCarmencita David Padilla, Stephen T S Lam
Clinical Dysmorphology|January 20, 2012
Macrocephaly-capillary malformation: a report of four Chinese patients and literature reviewHo Ming Luk, Ivan F M Lo, Carman W S Lai, et al.
American Journal of Medical Genetics. Part A|March 25, 2004
XX-agonadism in a fetus with multiple congenital anomaliesHennie H N Woo, Ivan F M Lo, H Y Tse, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|June 10, 2009
Novel PRPF31 and PRPH2 mutations and co-occurrence of PRPF31 and RHO mutations in Chinese patients with retinitis pigmentosaKing Poo Lim, Shea Ping Yip, Suk Chun Cheung, et al.
Clinical Biochemistry|February 25, 2006
High rate of detection of subtelomeric aberration by using combined MLPA and subtelomeric FISH approach in patients with moderate to severe mental retardationAlbert C F Lam, Stephen T S Lam, Kent K S Lai, et al.
Hong Kong Medical Journal = Xianggang Yi Xue Za Zhi|June 5, 2013
A young woman with mucocutaneous pigmentation and intestinal polypsH M Luk, Ivan F M Lo, Kelvin M C Yu, et al.
American Journal of Medical Genetics. Part A|March 16, 2013
A second report of p.Pro986Leu variant in COL2A1-phenotypic overlap with SEDC and other forms of type II collagenopathiesBrian H Y Chung, Ho-ming Luk, Ivan F M Lo, et al.
Clinical Biochemistry|January 18, 2006
Detecting exon deletions and duplications of the DMD gene using Multiplex Ligation-dependent Probe Amplification (MLPA)Kent K S Lai, Ivan F M Lo, Tony M F Tong, et al.
Chinese Medical Journal|October 20, 2005
Spectrum of NSD1 gene mutations in southern Chinese patients with Sotos syndromeTony M F Tong, Edgar W L Hau, Ivan F M Lo, et al.
Pageof 4

Showing results (1-10 of 31) with videos related to

Sort By:
Pageof 4
Beijing Da Xue Xue Bao. Yi Xue Ban = Journal of Peking University. Health Sciences|March 7, 2006
Experience of medical genetics in Hong KongStephen T S Lam
Annals of the Academy of Medicine, Singapore|November 12, 2009
Issues on universal screening for galactosemiaCarmencita David Padilla, Stephen T S Lam
Clinical Dysmorphology|January 20, 2012
Macrocephaly-capillary malformation: a report of four Chinese patients and literature reviewHo Ming Luk, Ivan F M Lo, Carman W S Lai, et al.
American Journal of Medical Genetics. Part A|March 25, 2004
XX-agonadism in a fetus with multiple congenital anomaliesHennie H N Woo, Ivan F M Lo, H Y Tse, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|June 10, 2009
Novel PRPF31 and PRPH2 mutations and co-occurrence of PRPF31 and RHO mutations in Chinese patients with retinitis pigmentosaKing Poo Lim, Shea Ping Yip, Suk Chun Cheung, et al.
Clinical Biochemistry|February 25, 2006
High rate of detection of subtelomeric aberration by using combined MLPA and subtelomeric FISH approach in patients with moderate to severe mental retardationAlbert C F Lam, Stephen T S Lam, Kent K S Lai, et al.
Hong Kong Medical Journal = Xianggang Yi Xue Za Zhi|June 5, 2013
A young woman with mucocutaneous pigmentation and intestinal polypsH M Luk, Ivan F M Lo, Kelvin M C Yu, et al.
American Journal of Medical Genetics. Part A|March 16, 2013
A second report of p.Pro986Leu variant in COL2A1-phenotypic overlap with SEDC and other forms of type II collagenopathiesBrian H Y Chung, Ho-ming Luk, Ivan F M Lo, et al.
Clinical Biochemistry|January 18, 2006
Detecting exon deletions and duplications of the DMD gene using Multiplex Ligation-dependent Probe Amplification (MLPA)Kent K S Lai, Ivan F M Lo, Tony M F Tong, et al.
Chinese Medical Journal|October 20, 2005
Spectrum of NSD1 gene mutations in southern Chinese patients with Sotos syndromeTony M F Tong, Edgar W L Hau, Ivan F M Lo, et al.
Pageof 4