Gary K. Mok
Lika, China
Last Updated: 09/26/2026
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Found 13 publications
Turner syndrome in diverse populations.
Journal: American journal of medical genetics. Part A
Published: September 11, 2019
Identifying the genetic causes for prenatally diagnosed structural congenital anomalies (SCAs) by whole-exome sequencing (WES).
Journal: BMC medical genomics
Published: August 24, 2018
Williams-Beuren syndrome in diverse populations.
Journal: American journal of medical genetics. Part A
Published: December 18, 2017
Noonan syndrome in diverse populations.
Journal: American journal of medical genetics. Part A
Published: May 05, 2017
Use of clinical chromosomal microarray in Chinese patients with autism spectrum disorder-implications of a copy number variation involving DPP10.
Journal: Molecular autism
Published: February 09, 2017
22q11.2 deletion syndrome in diverse populations.
Journal: American journal of medical genetics. Part A
Published: January 05, 2017
Down syndrome in diverse populations.
Journal: American journal of medical genetics. Part A
Published: August 31, 2016
De novo large rare copy-number variations contribute to conotruncal heart disease in Chinese patients.
Journal: NPJ genomic medicine
Published: April 14, 2016
Pathogenetics of alveolar capillary dysplasia with misalignment of pulmonary veins.
Journal: Human genetics
Published: January 08, 2016
Physical measurements of Chinese children in Hong Kong-A pilot study in preschools and kindergartens.
Journal: American journal of medical genetics. Part A
Published: November 13, 2015
The clinical impact of chromosomal microarray on paediatric care in Hong Kong.
Journal: PloS one
Published: May 14, 2014
Validation and application of health utilities index in Chinese subjects with down syndrome.
Journal: Health and quality of life outcomes
Published: March 19, 2014
Last Updated: 09/26/2026