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Unusual high number of spike protein mutations for the SARS-CoV-2 strains detected in Hong Kong

Journal of clinical virology, 2022-03, Vol.148, p.105081-105081, Article 105081

2022

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Grave impact of undetected rpoB I572F mutation on clinical course of multidrug-resistant tuberculosis: a case report

Hong Kong Medical Journal, 2023-02, Vol.29 (1), p.70-72

2023

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Aetiological bases of 46,XY disorders of sex development in the Hong Kong Chinese population

Hong Kong medical journal = Xianggang yi xue za zhi, 2015-12, Vol.21 (6), p.499-510

2015

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A frequent activated smoothened mutation in sporadic basal cell carcinomas

Oncogene, 1999-01, Vol.18 (3), p.833-836

1999

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Genetic basis of channelopathies and cardiomyopathies in Hong Kong Chinese patients: a 10-year regional laboratory experience

Hong Kong medical journal = Xianggang yi xue za zhi, 2018-08, Vol.24 (4), p.340-349

2018

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Heterogeneous mutations in the SLC3A1 and SLC7A9 genes in Chinese patients with cystinuria

Kidney international, 2006-01, Vol.69 (1), p.123-128

2006

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Atypical focal cortical dysplasia in a patient with Cowden syndrome

Hong Kong medical journal = Xianggang yi xue za zhi, 2014-04, Vol.20 (2), p.165-167

2014

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The clinical significance of aldosterone synthase deficiency: report of a novel mutation in the CYP11B2 gene

BMC endocrine disorders, 2014-04, Vol.14 (1), p.29-29, Article 29

2014

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Germline, somatic and epigenetic events underlying mismatch repair deficiency in colorectal and HNPCC-related cancers

Oncogene, 2002-10, Vol.21 (49), p.7585-7592

2002

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Early-onset colorectal cancer with stable microsatellite DNA and near-diploid chromosomes

Oncogene, 2001-08, Vol.20 (35), p.4871-4876

2001

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A Rett syndrome MECP2 mutation that causes mental retardation in men

Neurology, 2002-01, Vol.58 (2), p.226-230

2002

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Ketoconazole Induced Torsades de Pointes Without Concomitant Use of QT Interval‐Prolonging Drug

Journal of cardiovascular electrophysiology, 2005-12, Vol.16 (12), p.1375-1377

2005

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Galactorrhea—A strong clinical clue towards the diagnosis of neurotransmitter disease

Brain & development (Tokyo. 1979), 2006-07, Vol.28 (6), p.389-391

2006

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Alternative, noninvasive tissues for quantitative screening of mutant mitochondrial DNA

Clinical chemistry (Baltimore, Md.), 1997-07, Vol.43 (7), p.1241-1243

1997

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Mutations in the glucose-6-phosphate transporter (G6PT) gene in patients with glycogen storage diseases type 1b and 1c

FEBS letters, 1999-10, Vol.459 (2), p.255-258

1999

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Genetics of familial amyloidotic polyneuropathy in a Hong Kong Chinese kindred

Acta neurologica Scandinavica, 2003-06, Vol.107 (6), p.419-422

2003

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Novel mutation in the GRHPR gene in a Chinese patient with primary hyperoxaluria type 2 requiring renal transplantation from a living related donor

American journal of kidney diseases, 2001-12, Vol.38 (6), p.1307-1310

2001

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Novel mutation and polymorphisms of the HMBS gene detected by denaturing HPLC

Clinical chemistry (Baltimore, Md.), 2001-02, Vol.47 (2), p.343-346

2001

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Early-onset primary torsional dystonia in a 4-generation Chinese family with a mutation in the DYT1 gene

Chinese medical journal, 2005-05, Vol.118 (10), p.873-876

2005

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Linkage disequilibrium and linkage analysis of the glucose-6-phosphatase gene

Human genetics, 1998-08, Vol.103 (2), p.199-203

1998

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Magnetic resonance spectroscopy and analysis of MECP2 in Rett syndrome

Pediatric neurology, 2002-03, Vol.26 (3), p.205-209

2002

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Unusual high number of spike protein mutations for the SARS-CoV-2 strains detected in Hong Kong

Grave impact of undetected rpoB I572F mutation on clinical course of multidrug-resistant tuberculosis: a case report

Aetiological bases of 46,XY disorders of sex development in the Hong Kong Chinese population

A frequent activated smoothened mutation in sporadic basal cell carcinomas

Genetic basis of channelopathies and cardiomyopathies in Hong Kong Chinese patients: a 10-year regional laboratory experience

Heterogeneous mutations in the SLC3A1 and SLC7A9 genes in Chinese patients with cystinuria

Atypical focal cortical dysplasia in a patient with Cowden syndrome

The clinical significance of aldosterone synthase deficiency: report of a novel mutation in the CYP11B2 gene

Germline, somatic and epigenetic events underlying mismatch repair deficiency in colorectal and HNPCC-related cancers

Early-onset colorectal cancer with stable microsatellite DNA and near-diploid chromosomes

A Rett syndrome MECP2 mutation that causes mental retardation in men

Ketoconazole Induced Torsades de Pointes Without Concomitant Use of QT Interval‐Prolonging Drug

Galactorrhea—A strong clinical clue towards the diagnosis of neurotransmitter disease

Alternative, noninvasive tissues for quantitative screening of mutant mitochondrial DNA

Mutations in the glucose-6-phosphate transporter (G6PT) gene in patients with glycogen storage diseases type 1b and 1c

Genetics of familial amyloidotic polyneuropathy in a Hong Kong Chinese kindred

Novel mutation in the GRHPR gene in a Chinese patient with primary hyperoxaluria type 2 requiring renal transplantation from a living related donor

Novel mutation and polymorphisms of the HMBS gene detected by denaturing HPLC

Early-onset primary torsional dystonia in a 4-generation Chinese family with a mutation in the DYT1 gene

Linkage disequilibrium and linkage analysis of the glucose-6-phosphatase gene

Magnetic resonance spectroscopy and analysis of MECP2 in Rett syndrome

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