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Prenatal diagnosis and molecular cytogenetic characterization of fetuses with central nervous system anomalies using chromosomal microarray analysis: a seven-year single-center retrospective study

Scientific reports, 2024-01, Vol.14 (1), p.2271-2271, Article 2271

2024

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Molecular characterization of similar Hb Lepore Boston-Washington in four Chinese families using third generation sequencing

Scientific reports, 2024-04, Vol.14 (1), p.9966-8, Article 9966

2024

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Catalytic Degradation of Triphenylmethane Dyes with an Iron Porphyrin Complex as a Cytochrome P450 Model

Molecules (Basel, Switzerland), 2023-07, Vol.28 (14), p.5401

2023

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Prenatal diagnosis of fetuses with 15q11.2 BP1-BP2 microdeletion in the Chinese population: a seven-year single-center retrospective study

Molecular cytogenetics, 2024-09, Vol.17 (1), p.20-8, Article 20

2024

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Case Report: Prenatal Whole-Exome Sequencing Identified a Novel Nonsense Mutation of the KCNH2 Gene in a Fetus With Familial 2q14.2 Duplication

Frontiers in genetics, 2022-07, Vol.13

2022

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Case Report: Prenatal Diagnosis of a Novel Variant c.251dupT (p.N87Kfs6) in BCOR Resulting in Oculofaciocardiodental Syndrome Using Whole-Exome Sequencing

Frontiers in genetics, 2022-03, Vol.13, p.829613

2022

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Case Report: Novel compound heterozygous variants in CHRNA1 gene leading to lethal multiple pterygium syndrome: A case report

Frontiers in genetics, 2022-08, Vol.13

2022

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Prenatal whole exome sequencing identified two rare compound heterozygous variants in EVC2 causing Ellis-van Creveld syndrome

Molecular genetics & genomic medicine, 2023-10, Vol.11 (10), p.e2242-e2242

2023

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Etiological identification of recurrent male fatality due to a novel NSDHL gene mutation using trio whole‐exome sequencing: A rare case report and literature review

Molecular genetics & genomic medicine, 2023-03, Vol.11 (3), p.e2121-n/a

2023

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Identification of a Rare Variant of c.1777G>A (p.G593S) in the COL1A1 Gene as the Etiology of Recurrent Osteogenesis Imperfecta by Whole-Exome Sequencing

Frontiers in pediatrics, 2022-04, Vol.10, p.816090-816090

2022

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The Genetic Etiology Diagnosis of Fetal Growth Restriction Using Single-Nucleotide Polymorphism-Based Chromosomal Microarray Analysis

Frontiers in pediatrics, 2021-10, Vol.9, p.743639-743639

2021

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A surface-fluorinated-TiO2-KMnO4 photocatalytic system for determination of chemical oxygen demand

Analytica chimica acta, 2006-07, Vol.571 (2), p.242-247

2006

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Research on Building the Preference Model of Seamless Badminton Sportswear Based on the Conjoint Analysis

Advanced materials research, 2013, Vol.796, p.462-467

2013

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A First Clinical and Molecular Study of Rare IVS-II-806 (G > C) (HBB:c.316-45G > C) Variant in the β-globin Gene: A Possibly Benign Variant

Indian journal of hematology & blood transfusion, 2023-01, Vol.39 (1), p.102-106

2023

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Third‐generation sequencing identified two rare α‐chain variants leading to hemoglobin variants in Chinese population

Molecular genetics & genomic medicine, 2024-01, Vol.12 (1), p.e2365-n/a

2024

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A surface-fluorinated-TiO sub(2)-KMnO sub(4) photocatalytic system for determination of chemical oxygen demand

Analytica chimica acta, 2006-07, Vol.571 (2), p.242-247

2006

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Preparation method and industrialization of Ta-based ultra high temperature ceramic Tujia jar tea baking jar materials

Materials express, 2024-06, Vol.14 (6), p.914-921

2024

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Case Report: Prenatal Whole-Exome Sequencing Identified a Novel Nonsense Mutation of the KCNH2 Gene in a Fetus With Familial 2q14.2 Duplication

Frontiers in genetics, 2022, Vol.13, p.924573-924573

2022

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Case Report: Prenatal Diagnosis of a Novel Variant c.251dupT (p.N87Kfs6) in BCOR Resulting in Oculofaciocardiodental Syndrome Using Whole-Exome Sequencing

Frontiers in genetics, 2022, Vol.13, p.829613-829613

2022

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Case Report: Novel compound heterozygous variants in CHRNA1 gene leading to lethal multiple pterygium syndrome: A case report

Frontiers in genetics, 2022, Vol.13, p.964098-964098

2022

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A surface-fluorinated-TiO 2–KMnO 4 photocatalytic system for determination of chemical oxygen demand

Analytica chimica acta, 2006, Vol.571 (2), p.242-247

2006

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Identification of a Ubiquitin-Binding Structure in the S-Locus F-Box Protein Controlling S-RNase-Based Self-Incompatibility

遗传学报, 2012, Vol.39 (2), p.93-102

Guang Chen BinZhang Lijing Liu Qun Li Yu＇e Zhang Qi Xie Yongbiao Xue

2012

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Combination of modified nitrogen fertilizers and water saving irrigation can reduce greenhouse gas emissions and increase rice yield

Geoderma, 2018-04, Vol.315, p.1-10

2018

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Covert Communications in D2D Underlaying Cellular Networks With Antenna Array Assisted Artificial Noise Transmission

IEEE transactions on vehicular technology, 2020-03, Vol.69 (3), p.2980-2992

2020

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STRONG COMMUTATIVITY PRESERVING MAPS OF UPPER TRIANGULAR MATRIX LIE ALGEBRAS OVER A COMMUTATIVE RING

Taehan Suhakhoe hoebo, 2021, Vol.58 (4), p.973-981

2021

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Prenatal diagnosis and molecular cytogenetic characterization of fetuses with central nervous system anomalies using chromosomal microarray analysis: a seven-year single-center retrospective study

Molecular characterization of similar Hb Lepore Boston-Washington in four Chinese families using third generation sequencing

Catalytic Degradation of Triphenylmethane Dyes with an Iron Porphyrin Complex as a Cytochrome P450 Model

Prenatal diagnosis of fetuses with 15q11.2 BP1-BP2 microdeletion in the Chinese population: a seven-year single-center retrospective study

Case Report: Prenatal Whole-Exome Sequencing Identified a Novel Nonsense Mutation of the KCNH2 Gene in a Fetus With Familial 2q14.2 Duplication

Case Report: Prenatal Diagnosis of a Novel Variant c.251dupT (p.N87Kfs6) in BCOR Resulting in Oculofaciocardiodental Syndrome Using Whole-Exome Sequencing

Case Report: Novel compound heterozygous variants in CHRNA1 gene leading to lethal multiple pterygium syndrome: A case report

Prenatal whole exome sequencing identified two rare compound heterozygous variants in EVC2 causing Ellis-van Creveld syndrome

Etiological identification of recurrent male fatality due to a novel NSDHL gene mutation using trio whole‐exome sequencing: A rare case report and literature review

Identification of a Rare Variant of c.1777G>A (p.G593S) in the COL1A1 Gene as the Etiology of Recurrent Osteogenesis Imperfecta by Whole-Exome Sequencing

The Genetic Etiology Diagnosis of Fetal Growth Restriction Using Single-Nucleotide Polymorphism-Based Chromosomal Microarray Analysis

A surface-fluorinated-TiO2-KMnO4 photocatalytic system for determination of chemical oxygen demand

Research on Building the Preference Model of Seamless Badminton Sportswear Based on the Conjoint Analysis

A First Clinical and Molecular Study of Rare IVS-II-806 (G > C) (HBB:c.316-45G > C) Variant in the β-globin Gene: A Possibly Benign Variant

Third‐generation sequencing identified two rare α‐chain variants leading to hemoglobin variants in Chinese population

A surface-fluorinated-TiO sub(2)-KMnO sub(4) photocatalytic system for determination of chemical oxygen demand

Preparation method and industrialization of Ta-based ultra high temperature ceramic Tujia jar tea baking jar materials

Case Report: Prenatal Whole-Exome Sequencing Identified a Novel Nonsense Mutation of the KCNH2 Gene in a Fetus With Familial 2q14.2 Duplication

Case Report: Prenatal Diagnosis of a Novel Variant c.251dupT (p.N87Kfs6) in BCOR Resulting in Oculofaciocardiodental Syndrome Using Whole-Exome Sequencing

Case Report: Novel compound heterozygous variants in CHRNA1 gene leading to lethal multiple pterygium syndrome: A case report

A surface-fluorinated-TiO 2–KMnO 4 photocatalytic system for determination of chemical oxygen demand

Identification of a Ubiquitin-Binding Structure in the S-Locus F-Box Protein Controlling S-RNase-Based Self-Incompatibility

Combination of modified nitrogen fertilizers and water saving irrigation can reduce greenhouse gas emissions and increase rice yield

Covert Communications in D2D Underlaying Cellular Networks With Antenna Array Assisted Artificial Noise Transmission

STRONG COMMUTATIVITY PRESERVING MAPS OF UPPER TRIANGULAR MATRIX LIE ALGEBRAS OVER A COMMUTATIVE RING

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