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Co-inheritance of G6PD deficiency and 211 G to a variation of UGT1A1 in neonates with hyperbilirubinemia in eastern Guangdong

BMC pediatrics, 2021-12, Vol.21 (1), p.564-564, Article 564

2021

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Molecular epidemiological characterization and health burden of thalassemia in Jiangxi Province, P. R. China

PloS one, 2014-07, Vol.9 (7), p.e101505-e101505

2014

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Phenotype and Genotype Analysis in Two Pedigrees with Hereditary Coagulation Factor Ⅺ Deficiency

Sichuan da xue xue bao. Journal of Sichuan University. Yi xue ban, 2020-03, Vol.51 (2), p.252-256

2020

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Human serum albumin variants in China: a molecular epidemiological investigation and literature review

Journal of international medical research, 2021-12, Vol.49 (12), p.3000605211064225-3000605211064225

2021

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Hemoglobinopathy: molecular epidemiological characteristics and health effects on Hakka people in the Meizhou region, southern China

PloS one, 2013-02, Vol.8 (2), p.e55024-e55024

2013

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High resolution melting analysis: a rapid screening and typing tool for common β-thalassemia mutation in Chinese population

PloS one, 2014-08, Vol.9 (8), p.e102243-e102243

2014

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Gene variants in four pedigrees with hereditary coagulation factor XI deficiency and one novel mutation identification

Blood coagulation & fibrinolysis, 2020-03, Vol.31 (2), p.160

2020

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Hepatitis B virus infection and replication in primarily cultured human fetal hepatocytes

World journal of gastroenterology : WJG, 2007-02, Vol.13 (7), p.1027

2007

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Development and evaluation of a reverse dot blot assay for the simultaneous detection of common alpha and beta thalassemia in Chinese

Blood cells, molecules, & diseases, 2012-02, Vol.48 (2), p.86-90

2012

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Molecular Epidemiological Characterization and Health Burden of Thalassemias in the Chaoshan Region, People's Republic of China

Hemoglobin, 2016-03, Vol.40 (2), p.138-142

2016

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Genital human papillomavirus screening by gene chip in Chinese women of Guangdong province

Australian & New Zealand journal of obstetrics & gynaecology, 2008-04, Vol.48 (2), p.189-194

2008

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Hb CS-H disease combined with β-thalassemia-a case report

Blood cells, molecules, & diseases, 2010-04, Vol.44 (4), p.215-216

2010

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Clinical and molecular characterization of a rare 2.4kb deletion causing α+ thalassemia in a Chinese family

Blood cells, molecules, & diseases, 2012-08, Vol.49 (2), p.83-84

2012

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Molecular Epidemiological Survey of Hemoglobinopathies in the Wuxi Region of Jiangsu Province, Eastern China

Hemoglobin, 2013-01, Vol.37 (5), p.454-466

2013

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Hb Q-H disease: Two cases in a Cantonese family

Blood cells, molecules, & diseases, 2008-11, Vol.41 (3), p.259-260

2008

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Molecular and clinical characteristics of hemoglobin Ottawa detected in a Chinese population

Molecular medicine reports, 2011-05, Vol.4 (3), p.581-583

2011

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Three cases of the hemoglobin G-Chinese variant detected in patients of southern Chinese origin

Molecular medicine reports, 2010-05, Vol.3 (3), p.459-461

2010

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Hb G-Waimanalo: occurrence in combination with alpha-thalassemia-1 Southeast Asian deletion

Blood cells, molecules, & diseases, 2009, Vol.42 (1), p.36-37

2009

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High Resolution Melting Analysis: A Rapid Screening and Typing Tool for Common [beta]-Thalassemia Mutation in Chinese Population

PloS one, 2014-08, Vol.9 (8)

2014

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Clinical and molecular characterization of a rare 2.4 kb deletion causing α+ thalassemia in a Chinese family

Blood cells, molecules, & diseases, 2012-08, Vol.49 (2), p.83-84

2012

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Molecular characteristics of three hemoglobin variants observed in a Chinese population: Hb Ube-1 [β98 (FG5) Val→Met], Hb Ube‑2 [α68 (E17) Asn→Asp] and Hb Ube‑4 [α116 (GH4) Glu→Ala]

Molecular medicine reports, 2011-07, Vol.4 (4), p.681-685

2011

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Karyotype Stability and Unbiased Fractionation in the Paleo-Allotetraploid Cucurbita Genomes

Molecular plant, 2017-10, Vol.10 (10), p.1293-1306

2017

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Distributed dynamic backup servo control for satcom-on-the-move systems

Journal of physics. Conference series, 2024-05, Vol.2746 (1), p.12043

2024

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Hb CS-H disease combined with beta-thalassemia--a case report

Blood cells, molecules & diseases, 2010, Vol.44 (4), p.215-216

2010

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Water-trapping and drag-reduction effects of fish Ctenopharyngodon idellus scales and their simulations

Science China. Technological sciences, 2017-07, Vol.60 (7), p.1111-1117

2017

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Co-inheritance of G6PD deficiency and 211 G to a variation of UGT1A1 in neonates with hyperbilirubinemia in eastern Guangdong

Molecular epidemiological characterization and health burden of thalassemia in Jiangxi Province, P. R. China

Phenotype and Genotype Analysis in Two Pedigrees with Hereditary Coagulation Factor Ⅺ Deficiency

Human serum albumin variants in China: a molecular epidemiological investigation and literature review

Hemoglobinopathy: molecular epidemiological characteristics and health effects on Hakka people in the Meizhou region, southern China

High resolution melting analysis: a rapid screening and typing tool for common β-thalassemia mutation in Chinese population

Gene variants in four pedigrees with hereditary coagulation factor XI deficiency and one novel mutation identification

Hepatitis B virus infection and replication in primarily cultured human fetal hepatocytes

Development and evaluation of a reverse dot blot assay for the simultaneous detection of common alpha and beta thalassemia in Chinese

Molecular Epidemiological Characterization and Health Burden of Thalassemias in the Chaoshan Region, People's Republic of China

Genital human papillomavirus screening by gene chip in Chinese women of Guangdong province

Hb CS-H disease combined with β-thalassemia-a case report

Clinical and molecular characterization of a rare 2.4kb deletion causing α+ thalassemia in a Chinese family

Molecular Epidemiological Survey of Hemoglobinopathies in the Wuxi Region of Jiangsu Province, Eastern China

Hb Q-H disease: Two cases in a Cantonese family

Molecular and clinical characteristics of hemoglobin Ottawa detected in a Chinese population

Three cases of the hemoglobin G-Chinese variant detected in patients of southern Chinese origin

Hb G-Waimanalo: occurrence in combination with alpha-thalassemia-1 Southeast Asian deletion

High Resolution Melting Analysis: A Rapid Screening and Typing Tool for Common [beta]-Thalassemia Mutation in Chinese Population

Clinical and molecular characterization of a rare 2.4 kb deletion causing α+ thalassemia in a Chinese family

Molecular characteristics of three hemoglobin variants observed in a Chinese population: Hb Ube-1 [β98 (FG5) Val→Met], Hb Ube‑2 [α68 (E17) Asn→Asp] and Hb Ube‑4 [α116 (GH4) Glu→Ala]

Karyotype Stability and Unbiased Fractionation in the Paleo-Allotetraploid Cucurbita Genomes

Distributed dynamic backup servo control for satcom-on-the-move systems

Hb CS-H disease combined with beta-thalassemia--a case report

Water-trapping and drag-reduction effects of fish Ctenopharyngodon idellus scales and their simulations

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