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Molecular characterization of thalassemia and hemoglobinopathy in Southeastern China

Scientific reports, 2019-03, Vol.9 (1), p.3493-3493, Article 3493

2019

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The clinical value of hsa-miR-190b-5p in peripheral blood of pediatric β-thalassemia and its regulation on BCL11A expression

PloS one, 2023-10, Vol.18 (10), p.e0292031-e0292031

2023

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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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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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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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A survey of numerical methods for nonlinear filtering problems

Physica. D, 2007-06, Vol.230 (1), p.27-36

2007

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Molecular analysis and prenatal diagnosis of seven Chinese families with genetic epilepsy

Frontiers in neuroscience, 2023-05, Vol.17, p.1165601-1165601

2023

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Estimation under unknown correlation: covariance intersection revisited

IEEE transactions on automatic control, 2002-11, Vol.47 (11), p.1879-1882

2002

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Prenatal diagnosis of BACs‐on‐Beads assay in 1520 cases from Fujian Province, China

Molecular genetics & genomic medicine, 2020-10, Vol.8 (10), p.e1446-n/a

2020

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How to Tell a Bad Filter Through Monte Carlo Simulations

IEEE transactions on automatic control, 2007-07, Vol.52 (7), p.1302-1307

2007

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Comment on "One-Step Solution for the Multistep Out-of-Sequence-Measurement Problem in Tracking

IEEE transactions on aerospace and electronic systems, 2011-07, Vol.47 (3), p.2285-2288

2011

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Adaptive Control Design for Nonaffine Models Arising in Flight Control

Journal of guidance, control, and dynamics, 2004-03, Vol.27 (2), p.209-217

2004

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Comparing antenna conical scan algorithms for spacecraft position estimation

Journal of guidance, control, and dynamics, 2007-07, Vol.30 (4), p.1186-1189

2007

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The clinical value of hsa-miR-190b-5p in peripheral blood of pediatric [beta]-thalassemia and its regulation on BCL11A expression

PloS one, 2023-10, Vol.18 (10), p.e0292031

2023

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Mutation analysis of GJB2, SLC26A4, GJB3 and mtDNA12SrRNA genes in 251 non-syndromic hearing loss patients in Fujian, China

International journal of pediatric otorhinolaryngology, 2024-01, Vol.176, p.111777-111777, Article 111777

2024

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Diagnostic accuracy and value of chromosomal microarray analysis for chromosomal abnormalities in prenatal detection: A prospective clinical study

Medicine (Baltimore), 2021-05, Vol.100 (20), p.e25999-e25999

2021

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Identification of a novel 91.5 kb-deletion (αα) FJ in the α-globin gene cluster using single-molecule real-time (SMRT) sequencing

The journal of maternal-fetal & neonatal medicine, 2023-12, Vol.36 (2), p.2254890-2254890

2023

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Prenatal diagnosis of thalassemia in 695 pedigrees from southeastern China: a 10‐year follow‐up study

Journal of clinical laboratory analysis, 2021-10, Vol.35 (10), p.e23982-n/a

2021

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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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Application of the prenatal BACs-on-Beads™ assay for rapid prenatal detection of sex chromosome mosaicism

Molecular genetics and genomics : MGG, 2022-09, Vol.297 (5), p.1423-1438

2022

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Genetic research and clinical analysis of β‐globin gene cluster deletions in the Chinese population of Fujian province: A 14‐year single‐center experience

Journal of clinical laboratory analysis, 2022-02, Vol.36 (2), p.e24181-n/a

2022

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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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First report of the spectrum of δ‐globin gene mutations among women of reproductive age in Fujian area—Discrimination of δ‐thalassemia, α‐thalassemia, and Iron Deficiency Anemia

Journal of clinical laboratory analysis, 2020-11, Vol.34 (11), p.e23479-n/a

2020

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A novel PLS1 c.981+1G>A variant causes autosomal‐dominant hereditary hearing loss in a family

Clinical genetics, 2023-04, Vol.103 (4), p.413-423

2023

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Analysis of genotype–phenotype correlation in patients with α‐thalassemia from Fujian province, Southeastern China

Journal of clinical laboratory analysis, 2022-10, Vol.36 (10), p.e24696-n/a

2022

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Molecular characterization of thalassemia and hemoglobinopathy in Southeastern China

The clinical value of hsa-miR-190b-5p in peripheral blood of pediatric β-thalassemia and its regulation on BCL11A expression

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

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

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

A survey of numerical methods for nonlinear filtering problems

Molecular analysis and prenatal diagnosis of seven Chinese families with genetic epilepsy

Estimation under unknown correlation: covariance intersection revisited

Prenatal diagnosis of BACs‐on‐Beads assay in 1520 cases from Fujian Province, China

How to Tell a Bad Filter Through Monte Carlo Simulations

Comment on "One-Step Solution for the Multistep Out-of-Sequence-Measurement Problem in Tracking

Adaptive Control Design for Nonaffine Models Arising in Flight Control

Comparing antenna conical scan algorithms for spacecraft position estimation

The clinical value of hsa-miR-190b-5p in peripheral blood of pediatric [beta]-thalassemia and its regulation on BCL11A expression

Mutation analysis of GJB2, SLC26A4, GJB3 and mtDNA12SrRNA genes in 251 non-syndromic hearing loss patients in Fujian, China

Diagnostic accuracy and value of chromosomal microarray analysis for chromosomal abnormalities in prenatal detection: A prospective clinical study

Identification of a novel 91.5 kb-deletion (αα) FJ in the α-globin gene cluster using single-molecule real-time (SMRT) sequencing

Prenatal diagnosis of thalassemia in 695 pedigrees from southeastern China: a 10‐year follow‐up study

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

Application of the prenatal BACs-on-Beads™ assay for rapid prenatal detection of sex chromosome mosaicism

Genetic research and clinical analysis of β‐globin gene cluster deletions in the Chinese population of Fujian province: A 14‐year single‐center experience

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

First report of the spectrum of δ‐globin gene mutations among women of reproductive age in Fujian area—Discrimination of δ‐thalassemia, α‐thalassemia, and Iron Deficiency Anemia

A novel PLS1 c.981+1G>A variant causes autosomal‐dominant hereditary hearing loss in a family

Analysis of genotype–phenotype correlation in patients with α‐thalassemia from Fujian province, Southeastern China

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