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Yvonne K. Kwok

The Chinese University of Hong Kong

27

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409

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

2021 Frontiers in Genetics
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The role of chromosomal microarray analysis among fetuses with normal karyotype and single system anomaly or nonspecific sonographic findings.

2020 Acta Obstetricia et Gynecologica Scandinavica
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Recent Advances in the Noninvasive Prenatal Testing for Chromosomal Abnormalities Using Maternal Plasma DNA

2020 Journal of Fetal Medicine
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Clinical utility of expanded noninvasive prenatal screening and chromosomal microarray analysis in high risk pregnancies

2020 Ultrasound in Obstetrics & Gynecology
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Deciphering the complexity of simple chromosomal insertions by genome sequencing

2020 Human Genetics
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The utility of genome-wide cell-free DNA screening in the prenatal diagnosis of Pallister-Killian syndrome.

2020 Prenatal Diagnosis
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Clinical Significance of Non-Invasive Prenatal Screening for Trisomy 7: Cohort Study and Literature Review.

2020 Genes
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Prenatal Diagnosis of Fetuses with Increased Nuchal Translucency by Genome Sequencing Analysis

2019 Frontiers in Genetics
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Characteristics and mode of inheritance of pathogenic copy number variants in prenatal diagnosis

2019 American Journal of Obstetrics and Gynecology
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Prenatal Diagnosis of Fetuses with Increased Nuchal Translucency by Genome Sequencing Analysis

2019 bioRxiv
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