Ho-ming M. Luk

2 Kwong Lee Road
Sham Shui Po, KSS, Hong Kong Special Administrative Region

Last Updated: 09/26/2026

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Found 87 publications

Hereditary leiomyomatosis and renal cell carcinoma: a case series.

Hereditary leiomyomatosis and renal cell carcinoma: a case series.

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

Published: July 27, 2026

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

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

Journal: The Cleft palate-craniofacial journal : official publication of the American Cleft Palate-Craniofacial Association

Published: March 16, 2026

Correction: Protein domain-specific genotype-phenotype correlation study of neurofibromatosis type 1.

Correction: Protein domain-specific genotype-phenotype correlation study of neurofibromatosis type 1.

Journal: Scientific reports

Published: February 25, 2026

Early prenatal detection of autosomal dominant skeletal dysplasia using first-trimester ultrasound and cell-free fetal DNA screening: three case reports.

Early prenatal detection of autosomal dominant skeletal dysplasia using first-trimester ultrasound and cell-free fetal DNA screening: three case reports.

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

Published: January 27, 2026

Van der Woude syndrome with novel variants: a case series.

Van der Woude syndrome with novel variants: a case series.

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

Published: December 04, 2025

Additional case report supports loss-of-function CCNK variants being causative for a recognizable syndromic neurodevelopmental disorder.

Additional case report supports loss-of-function CCNK variants being causative for a recognizable syndromic neurodevelopmental disorder.

Journal: Clinical dysmorphology

Published: August 22, 2025

Long-term outcomes in 45,X/46,XY mosaicism: a 30-year retrospective study in Hong Kong.

Long-term outcomes in 45,X/46,XY mosaicism: a 30-year retrospective study in Hong Kong.

Journal: Annals of pediatric endocrinology & metabolism

Published: August 08, 2025

First case report of STAG2 -associated syndromic disorder resulting from partial exon deletion inherited from asymptomatic mosaic carrier mother.

First case report of STAG2 -associated syndromic disorder resulting from partial exon deletion inherited from asymptomatic mosaic carrier mother.

Journal: Clinical dysmorphology

Published: August 05, 2025

Spectrum of inherited eye disorders at Hong Kong Children's Hospital: insights into the local genetic landscape and experience with ocular genetic services.

Spectrum of inherited eye disorders at Hong Kong Children's Hospital: insights into the local genetic landscape and experience with ocular genetic services.

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

Published: August 04, 2025

Protein domain-specific genotype-phenotype correlation study of neurofibromatosis type 1.

Protein domain-specific genotype-phenotype correlation study of neurofibromatosis type 1.

Journal: Scientific reports

Published: July 10, 2025

Protein domain-specific genotype-phenotype correlation study of neurofibromatosis type 1.

Protein domain-specific genotype-phenotype correlation study of neurofibromatosis type 1.

Journal: Scientific reports

Published: July 10, 2025

Familial SIN3A-associated Witteveen-Kolk syndrome in a Chinese family with prominent ectodermal dysplasia, progeroid appearance, and early onset diabetes mellitus.

Familial SIN3A-associated Witteveen-Kolk syndrome in a Chinese family with prominent ectodermal dysplasia, progeroid appearance, and early onset diabetes mellitus.

Journal: Clinical dysmorphology

Published: June 30, 2025

Showing 1-12 of 87

Last Updated: 09/26/2026