Publications by authors named "Fai Man Lo"

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Characterization of Factors Associated With Death in Deceased Patients With Mitochondrial Disorders: A Multicenter Cross-Sectional Survey.
Alina Ivaniuk, Irina A Anselm, Aaron Bowen, Bruce H Cohen, Fatma Tuba Eminoglu, Piervito Lopriore, Michelangelo Mancuso, Sin-Ying Florence Fan, Fai-Man Lo

Neurology· February 2025

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Mitochondrial diseases in Hong Kong: prevalence, clinical characteristics and genetic landscape.
Tsz-Sum Wong, Kiran M Belaramani, Chun-Kong Chan, Wing-Ki Chan, Wai-Lun Larry Chan, Sin-Ying Florence Fan, Fai-Man Lo

Orphanet J Rare Dis· March 2023

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Health professionals' involvement and information provision in genetic counseling following prenatal diagnosis of sex chromosome aneuploidy in Hong Kong.
Po Lam So, Yvonne Kwun Yue Cheng, Kwan Yiu Cheuk, Wan Kam Chiu, Shui Lam Mak, Tsz Kin Lo, Fai Man Lo

Int J Gynaecol Obstet· March 2019

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Parental decisions following prenatal diagnosis of sex chromosome aneuploidy in Hong Kong.
Po Lam So, Kwun Yue Yvonne Cheng, Kwan Yiu Cheuk, Wan Kam Chiu, Shui Lam Mak, Tsz Kin Lo, Fai Man Lo

J Obstet Gynaecol Res· December 2017

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Validation of a robust PCR-based assay for quantifying fragile X CGG repeats.
Yvonne K Kwok, Kit Man Wong, Fai Man Lo, Grace Wing Shan Kong, J Kent Moore

Clin Chim Acta· May 2016

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Recurrent structural malformations identified among Mowat-Wilson syndrome fetuses.
Yan Zhou, Jin Huang, Yvonne Kwun Yue Cheng, Tak Yeung Leung, Ritsuko K Pooh, Fai Man Lo

Prenat Diagn· March 2014

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Molecular basis of von Hippel-Lindau syndrome in Chinese patients.
Wai-Kwan Siu, Ronald Ching-Wan Ma, Ching-Wan Lam, Chloe Miu Mak, Yuet-Ping Yuen, Fai-Man Ivan Lo

Chin Med J (Engl)· January 2011

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PHOX2B mutations in three Chinese patients with congenital central hypoventilation syndrome.
Siu-Fong June Or, Ming-for Tony Tong, Fai-Man Ivan Lo, Chi-Wai Law, Ting-Yat Miu

Chin Med J (Engl)· October 2006

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Three novel FOXL2 gene mutations in Chinese patients with blepharophimosis-ptosis-epicanthus inversus syndrome.
Siu-fong June Or, Ming-for Tony Tong, Fai-man Ivan Lo, Tak-sum Stephen Lam

Chin Med J (Engl)· January 2006

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Wisconsin syndrome in a patient with interstitial deletion of the long arm of chromosome 3: further delineation of the phenotype.
Wai-tai Ko, Wai-fan Lam, Fai-man Lo, Wing-kwong Chan, Tak-sum Lam

Am J Med Genet A· July 2003

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Novel mutations in the PATCHED gene in basal cell nevus syndrome.
Ching-Wan Lam, Chi-Yan Leung, Kam-Cheong Lee, Jingwu Xie, Fai-Man Lo, Loi-Yuen Chan

Mol Genet Metab· May 2002

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