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List of works by Luk Ho-Ming

Adult Chinese twins with Kenny-Caffey syndrome type 2: A potential age-dependent phenotype and review of literature

scientific article published on 01 December 2020

Adult Prader-Willi Syndrome: An Update on Management.

scientific article

CHARGE syndrome in nine patients from China

scientific article published on 15 November 2019

Clinical and molecular characterization study of Chinese Kabuki syndrome in Hong Kong

scientific article published on 13 December 2020

Coffin-Lowry syndrome in Chinese

scientific article published on 09 August 2019

Congenital titinopathy: Comprehensive characterisation and pathogenic insights

scientific article published on 25 April 2018

Evolving clinical manifestations of mandibular hypoplasia, deafness, progeroid features, and lipodystrophy syndrome: From infancy to adulthood in a 31-year-old woman

scientific article published on 23 December 2020

HIST1H1E heterozygous protein-truncating variants cause a recognizable syndrome with intellectual disability and distinctive facial gestalt: A study to clarify the HIST1H1E syndrome phenotype in 30 individuals

scientific article published on 09 August 2019

Mosaic KRAS mutation in a patient with encephalocraniocutaneous lipomatosis and renovascular hypertension

scientific article published on 05 October 2018

Phenotypic and mutational spectrum of 21 Chinese patients with Alström syndrome

scientific article published on 22 November 2019

Prenatal and postnatal diagnosis of Schuurs-Hoeijmakers syndrome: Case series and review of the literature

scientific article published on 09 November 2020

Rubinstein-Taybi syndrome in Chinese population with four novel mutations

scientific article published on 16 October 2020

Rubinstein-Taybi syndrome in diverse populations

scientific article published on 27 September 2020

Williams–Beuren syndrome in diverse populations

scientific article published in May 2018

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