Stephanie K L Ho

7PUBLICATIONS
7CO-AUTHORS
Infant and child healthGene expression (incl. microarray and other genome-wide approaches)Developmental genetics (incl. sex determination)Molecular imaging (incl. electron microscopy and neutron diffraction)Major global burdens of disease
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Publications (7)

|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

|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

|Feb 17, 2022
KBG syndrome in a Chinese population: A case series.

Stephanie Ho, Ho-Ming Luk, Ivan F M Lo

|Jan 10, 2022
The first case report of Strømme syndrome in a Chinese patient: Expanding the phenotype and literature review.

Stephanie Ho, Ho-Ming Luk, Ivan F M Lo

|Nov 19, 2021
Extending the phenotype of DeSanto-Shinawi syndrome: A case report and literature review.

Stephanie Ho, Ho-Ming Luk, Ivan F M Lo

|Sep 24, 2021
CTNNB1-related neurodevelopmental disorder in a Chinese population: A case series.

Stephanie Ho, Mandy Ho-Yin Tsang, Jasmine Lee-Fong Fung

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Frequent Collaborators

5 joint publications

Ho-Ming Luk

2 joint publications

Wing Chung Yiu

1 joint publications

Brian Hon-Yin Chung

1 joint publications

Jennifer Y Y Poon