Yvonne K. Kwok

Sar, China

Last Updated: 09/26/2026

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Found 20 publications

Genetic Investigation of X-Linked Defects with Optimized Targeted Long-Read Sequencing.

Genetic Investigation of X-Linked Defects with Optimized Targeted Long-Read Sequencing.

Journal: Clinical chemistry

Published: April 02, 2026

Mate-pair low-pass genome sequencing for prenatal diagnosis of fetuses with ultrasound anomalies: abridged secondary publication.

Mate-pair low-pass genome sequencing for prenatal diagnosis of fetuses with ultrasound anomalies: abridged secondary publication.

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

Published: November 07, 2025

Amniotic fluid gamma-glutamyl transferase for prediction of biliary atresia in cases of non-visualisation of the fetal gallbladder: a retrospective study using a validated analytical platform and local reference range.

Amniotic fluid gamma-glutamyl transferase for prediction of biliary atresia in cases of non-visualisation of the fetal gallbladder: a retrospective study using a validated analytical platform and local reference range.

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

Published: June 04, 2024

Low-Pass Genome Sequencing-Based Detection of Paternity: Validation in Clinical Cytogenetics.

Low-Pass Genome Sequencing-Based Detection of Paternity: Validation in Clinical Cytogenetics.

Journal: Genes

Published: May 12, 2023

Mate-pair genome sequencing reveals structural variants for idiopathic male infertility.

Mate-pair genome sequencing reveals structural variants for idiopathic male infertility.

Journal: Human genetics

Published: October 28, 2022

TEDD: a database of temporal gene expression patterns during multiple developmental periods in human and model organisms.

TEDD: a database of temporal gene expression patterns during multiple developmental periods in human and model organisms.

Journal: Nucleic acids research

Published: August 09, 2022

Investigation of the genetic etiology in male infertility with apparently balanced chromosomal structural rearrangements by genome sequencing.

Investigation of the genetic etiology in male infertility with apparently balanced chromosomal structural rearrangements by genome sequencing.

Journal: Asian journal of andrology

Published: January 12, 2022

Trio-Based Low-Pass Genome Sequencing Reveals Characteristics and Significance of Rare Copy Number Variants in Prenatal Diagnosis.

Trio-Based Low-Pass Genome Sequencing Reveals Characteristics and Significance of Rare Copy Number Variants in Prenatal Diagnosis.

Journal: Frontiers in genetics

Published: July 16, 2021

Low-pass genome sequencing-based detection of absence of heterozygosity: validation in clinical cytogenetics.

Low-pass genome sequencing-based detection of absence of heterozygosity: validation in clinical cytogenetics.

Journal: Genetics in medicine : official journal of the American College of Medical Genetics

Published: October 07, 2020

The role of chromosomal microarray analysis among fetuses with normal karyotype and single system anomaly or nonspecific sonographic findings.

The role of chromosomal microarray analysis among fetuses with normal karyotype and single system anomaly or nonspecific sonographic findings.

Journal: Acta obstetricia et gynecologica Scandinavica

Published: June 18, 2020

Deciphering the complexity of simple chromosomal insertions by genome sequencing.

Deciphering the complexity of simple chromosomal insertions by genome sequencing.

Journal: Human genetics

Published: June 09, 2020

Low-pass genome sequencing: a validated method in clinical cytogenetics.

Low-pass genome sequencing: a validated method in clinical cytogenetics.

Journal: Human genetics

Published: March 11, 2020

Showing 1-12 of 20

Last Updated: 09/26/2026