Kelvin K. Chan
Sar, China
Last Updated: 09/26/2026
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Found 25 publications
Prenatal Phenotype in a Neonate with Prader-Willi Syndrome and Literature Review.
Journal: Diagnostics (Basel, Switzerland)
Published: April 25, 2025
Ivabradine induces RAD51 degradation, potentiating PARP inhibitor efficacy in non-germline BRCA pathogenic variant triple-negative breast cancer.
Journal: Journal of translational medicine
Published: April 11, 2025
Fetal Hyperthyroidism with Maternal Hypothyroidism: Two Cases of Intrauterine Therapy.
Journal: Diagnostics (Basel, Switzerland)
Published: November 07, 2023
Application of Prenatal Whole Exome Sequencing for Structural Congenital Anomalies-Experience from a Local Prenatal Diagnostic Laboratory.
Journal: Healthcare (Basel, Switzerland)
Published: October 27, 2022
Evaluating the Clinical Utility of Genome Sequencing for Cytogenetically Balanced Chromosomal Abnormalities in Prenatal Diagnosis.
Journal: Frontiers in genetics
Published: October 22, 2020
Increasing prenatal diagnosis of chimeras with the use of noninvasive prenatal screening: Report of two cases.
Journal: Prenatal diagnosis
Published: September 27, 2020
The KLHL40 c.1516A>C is a Chinese-specific founder mutation causing nemaline myopathy 8: Report of six patients with pre- and postnatal phenotypes.
Journal: Molecular genetics & genomic medicine
Published: February 02, 2020
A Small-Molecule AIE Chromosome Periphery Probe for Cytogenetic Studies.
Journal: Angewandte Chemie (International ed. in English)
Published: December 30, 2019
Cost-effectiveness analysis of chromosomal microarray as a primary test for prenatal diagnosis in Hong Kong.
Journal: BMC pregnancy and childbirth
Published: April 08, 2019
Prenatal diagnosis of 5p deletion syndrome: Report of five cases.
Journal: The journal of obstetrics and gynaecology research
Published: August 27, 2018
Last Updated: 09/26/2026