Nai-chung C. Fong

Hong Kong Special Administrative Region

Last Updated: 09/26/2026

Save publications for later

Sign Up

Not sure about your diagnosis?

Check Your Symptoms

Found 9 publications

Paediatric multisystem inflammatory syndrome temporally associated with SARS-CoV-2: a case report.

Paediatric multisystem inflammatory syndrome temporally associated with SARS-CoV-2: a case report.

Journal: Hong Kong medical journal = Xianggang yi xue za zhi

Published: March 07, 2022

Novel finding of lissencephaly and severe osteopenia in a Chinese patient with SATB2-associated syndrome and a brief review of literature.

Novel finding of lissencephaly and severe osteopenia in a Chinese patient with SATB2-associated syndrome and a brief review of literature.

Journal: American journal of medical genetics. Part A

Published: September 23, 2021

Using artificial intelligence as an initial triage strategy in diabetic retinopathy screening program in China

Using artificial intelligence as an initial triage strategy in diabetic retinopathy screening program in China

Journal: Zhonghua yi xue za zhi

Published: December 29, 2020

Centrosome-associated CDC25B is a novel disease-causing gene for a syndrome with cataracts, dilated cardiomyopathy, and multiple endocrinopathies.

Centrosome-associated CDC25B is a novel disease-causing gene for a syndrome with cataracts, dilated cardiomyopathy, and multiple endocrinopathies.

Journal: Clinica chimica acta; international journal of clinical chemistry

Published: November 01, 2019

Sudden arrhythmia death syndrome in young victims: a five-year retrospective review and two-year prospective molecular autopsy study by next-generation sequencing and clinical evaluation of their first-degree relatives.

Sudden arrhythmia death syndrome in young victims: a five-year retrospective review and two-year prospective molecular autopsy study by next-generation sequencing and clinical evaluation of their first-degree relatives.

Journal: Hong Kong medical journal = Xianggang yi xue za zhi

Published: January 24, 2019

Clinical whole-exome sequencing reveals a common pathogenic variant in patients with CoQ10 deficiency: An underdiagnosed cause of mitochondriopathy.

Clinical whole-exome sequencing reveals a common pathogenic variant in patients with CoQ10 deficiency: An underdiagnosed cause of mitochondriopathy.

Journal: Clinica chimica acta; international journal of clinical chemistry

Published: July 30, 2018

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

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

Journal: Hong Kong medical journal = Xianggang yi xue za zhi

Published: March 03, 2018

Diagnostic yield of array CGH in patients with autism spectrum disorder in Hong Kong.

Diagnostic yield of array CGH in patients with autism spectrum disorder in Hong Kong.

Journal: Clinical and translational medicine

Published: December 01, 2015

Clinical whole-exome sequencing reveals a novel missense pathogenic variant of GNAO1 in a patient with infantile-onset epilepsy.

Clinical whole-exome sequencing reveals a novel missense pathogenic variant of GNAO1 in a patient with infantile-onset epilepsy.

Journal: Clinica chimica acta; international journal of clinical chemistry

Published: August 26, 2015

Showing 1-9 of 9

Last Updated: 09/26/2026