Luk Ho-Ming

27PUBLICATIONS
156CO-AUTHORS
Gene expression (incl. microarray and other genome-wide approaches)Infant and child healthNeonatologyMajor global burdens of diseaseGenomics
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Publications (27)

|Jul 03, 2026
Leveraging Next-Generation Phenotyping in Dysmorphology to Support Variant Interpretation in Mowat-Wilson Syndrome.

|Mar 16, 2026
Cleft Lip and Palate is Common in PORCN-Related Focal Dermal Hypoplasia in Asians: Three New Case Reports and Literature Review.

Joshua C K Chan, Phoebe K W Wu, Wing Chung Yiu

|Nov 01, 2025
An Uncommon Case of Hypophosphataemia-Non-Lethal Raine Syndrome With Novel FAM20C Variant: Expanding the Phenotypic Spectrum.

Candice Wai-Man Au, Shirley Sze-Wing Cheng, Timothy Hua-Tse Cheng

|Jul 24, 2025
Waardenburg Syndrome: Review of Genotype-Phenotype Relationships in 30 Patients in Hong Kong.

Jennifer Y Y Poon, W C Yiu, Stephanie K L Ho

|Jan 30, 2025
Characterization of Factors Associated With Death in Deceased Patients With Mitochondrial Disorders: A Multicenter Cross-Sectional Survey.

Alina Ivaniuk, Irina A Anselm, Aaron Bowen

|Nov 11, 2022
Implementation of Public Funded Genome Sequencing in Evaluation of Fetal Structural Anomalies.

Po Lam So, Annie Shuk Yi Hui, Teresa Wei Ling Ma

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Frequent Collaborators

6 joint publications

Shirley Sze-Wing Cheng

5 joint publications

Stephanie K L Ho

4 joint publications

Hon-Yin B Chung

3 joint publications

Pui-Tak Yu