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A study on the standardization of muckmelon culture technique

Chung-kuo nung yeh kʿo hsüeh, 1989-06, Vol.22 (3)

1989

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Detection of copy number variation associated with ventriculomegaly in fetuses using single nucleotide polymorphism arrays

Scientific reports, 2021-03, Vol.11 (1), p.5291-5291, Article 5291

2021

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Efficiency of expanded noninvasive prenatal testing in the detection of fetal subchromosomal microdeletion and microduplication in a cohort of 31,256 single pregnancies

Scientific reports, 2022-11, Vol.12 (1), p.19750-19750, Article 19750

2022

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Genetic analysis of chorionic villus tissues in early missed abortions

Scientific reports, 2023-12, Vol.13 (1), p.21719-21719, Article 21719

2023

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Prenatal genetic analysis of fetal aberrant right subclavian artery with or without additional ultrasound anomalies in a third level referral center

Scientific reports, 2023-02, Vol.13 (1), p.3414-3414, Article 3414

2023

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Prenatal genetic diagnosis of fetuses with dextrocardia using whole exome sequencing in a tertiary center

Scientific reports, 2024-07, Vol.14 (1), p.16266-14, Article 16266

2024

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Genetic testing for fetal loss of heterozygosity using single nucleotide polymorphism array and whole-exome sequencing

Scientific reports, 2024-01, Vol.14 (1), p.2190-2190, Article 2190

2024

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Improvement in creep life of a nickel-based single-crystal superalloy via composition homogeneity on the multiscales by magnetic-field-assisted directional solidification

Scientific reports, 2018-01, Vol.8 (1), p.1452-17, Article 1452

2018

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Genetic Diagnostic Yield and Novel Causal Genes of Congenital Heart Disease

Frontiers in genetics, 2022-07, Vol.13

2022

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Inflammatory cytokines via up-regulation of aquaporins deteriorated the pathogenesis of early osteoarthritis

PloS one, 2019-08, Vol.14 (8), p.e0220846-e0220846

2019

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Clinical findings and genetic analysis of patients with copy number variants involving 17p13.3 using a single nucleotide polymorphism array: a single-center experience

BMC medical genomics, 2022-12, Vol.15 (1), p.268-10, Article 268

2022

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Prenatal diagnosis of fetuses with region of homozygosity detected by single nucleotide polymorphism array: a retrospective cohort study

Journal of human genetics, 2022-11, Vol.67 (11), p.629-638

2022

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ALKBH5 targets ACSL4 mRNA stability to modulate ferroptosis in hyperbilirubinemia-induced brain damage

Free radical biology & medicine, 2024-08, Vol.220, p.271-287

2024

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Long-Molecule Sequencing: A New Approach for Identification of Clinically Significant DNA Variants in α-Thalassemia and β-Thalassemia Carriers

The Journal of molecular diagnostics : JMD, 2020-08, Vol.22 (8), p.1087-1095

2020

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Single nucleotide polymorphism array analysis of 102 patients with developmental delay and/or intellectual disability from Fujian, China

Clinica chimica acta, 2020-11, Vol.510, p.638-643

2020

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Prenatal diagnosis of PLP1 duplication by single nucleotide polymorphism array in a family with Pelizaeus-Merzbacher disease

Aging (Albany, NY.), 2021-01, Vol.13 (1), p.1488-1497

2021

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Prenatal diagnosis and molecular cytogenetic identification of small supernumerary marker chromosomes: analysis of three prenatal cases using chromosome microarray analysis

Aging (Albany, NY.), 2020-12, Vol.13 (2), p.2135-2148

2020

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Numerical Investigation of the Dynamic Response of a Sand Cushion with Multiple Rockfall Impacts

Sustainability, 2023-02, Vol.15 (4), p.3554

2023

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Quadruplex real-time polymerase chain reaction assay for molecular diagnosis of Y-chromosomal microdeletions

Fertility and sterility, 2012-04, Vol.97 (4), p.864-869

2012

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Molecular Epidemiology of Group B Streptococcus Isolates from Pregnant Women with Premature Rupture of Membranes in Fuzhou, China

Infection and drug resistance, 2023-01, Vol.16, p.269-278

2023

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Long-Molecule Sequencing

The Journal of molecular diagnostics : JMD, 2020-08, Vol.22 (8), p.1087-1095

2020

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A study on the standardization of muckmelon culture technique

Detection of copy number variation associated with ventriculomegaly in fetuses using single nucleotide polymorphism arrays

Efficiency of expanded noninvasive prenatal testing in the detection of fetal subchromosomal microdeletion and microduplication in a cohort of 31,256 single pregnancies

Genetic analysis of chorionic villus tissues in early missed abortions

Prenatal genetic analysis of fetal aberrant right subclavian artery with or without additional ultrasound anomalies in a third level referral center

Prenatal genetic diagnosis of fetuses with dextrocardia using whole exome sequencing in a tertiary center

Genetic testing for fetal loss of heterozygosity using single nucleotide polymorphism array and whole-exome sequencing

Improvement in creep life of a nickel-based single-crystal superalloy via composition homogeneity on the multiscales by magnetic-field-assisted directional solidification

Genetic Diagnostic Yield and Novel Causal Genes of Congenital Heart Disease

Inflammatory cytokines via up-regulation of aquaporins deteriorated the pathogenesis of early osteoarthritis

Clinical findings and genetic analysis of patients with copy number variants involving 17p13.3 using a single nucleotide polymorphism array: a single-center experience

Prenatal diagnosis of fetuses with region of homozygosity detected by single nucleotide polymorphism array: a retrospective cohort study

ALKBH5 targets ACSL4 mRNA stability to modulate ferroptosis in hyperbilirubinemia-induced brain damage

Long-Molecule Sequencing: A New Approach for Identification of Clinically Significant DNA Variants in α-Thalassemia and β-Thalassemia Carriers

Single nucleotide polymorphism array analysis of 102 patients with developmental delay and/or intellectual disability from Fujian, China

Prenatal diagnosis of PLP1 duplication by single nucleotide polymorphism array in a family with Pelizaeus-Merzbacher disease

Prenatal diagnosis and molecular cytogenetic identification of small supernumerary marker chromosomes: analysis of three prenatal cases using chromosome microarray analysis

Numerical Investigation of the Dynamic Response of a Sand Cushion with Multiple Rockfall Impacts

Quadruplex real-time polymerase chain reaction assay for molecular diagnosis of Y-chromosomal microdeletions

Molecular Epidemiology of Group B Streptococcus Isolates from Pregnant Women with Premature Rupture of Membranes in Fuzhou, China

Long-Molecule Sequencing

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