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Role of Fetal Blood Sampling in the Prenatal Diagnosis of Thalassemia

Balkan medical journal, 2023-09, Vol.40 (5), p.380-381

2023

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Prenatal control of nondeletional α-thalassemia: first experience in mainland China

Prenatal diagnosis, 2013-09, Vol.33 (9), p.869-872

2013

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Apparent germline mosaicism for a 15q11-q13 deletion causing recurrent Angelman syndrome in a Chinese family

European journal of obstetrics & gynecology and reproductive biology, 2019-05, Vol.236, p.255-257

2019

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Co-inheritance of α-thalassaemia and β-thalassaemia in a prenatal screening population in mainland China

Journal of medical screening, 2014-12, Vol.21 (4), p.167-171

2014

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Pre Gestational Thalassemia Screening in Mainland China: The First Two Years of a Preventive Program

Hemoglobin, 2017-11, Vol.41 (4-6), p.248-253

2017

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Pathologic evaluation of uterine leiomyoma treated with radiofrequency ablation

International journal of gynecology and obstetrics, 2007-10, Vol.99 (1), p.9-13

2007

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A Krüppel-Like Factor 1 Gene Mutation Ameliorates the Severity of β-Thalassemia: A Case Report

Hemoglobin, 2019-03, Vol.43 (2), p.137-139

2019

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Evidence of Selection for the α-Globin Gene Deletions and Triplications in a Southern Chinese Population

Hemoglobin, 2015-11, Vol.39 (6), p.442-444

2015

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Hb Hornchurch [β43(CD2)Glu→Lys; HBB: c.130G>A] Compromises the Molecular Diagnosis of β-Thalassemia in a Chinese Family

Hemoglobin, 2017-11, Vol.41 (4-6), p.274-277

2017

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Hydrops Fetalis Associated with Compound Heterozygosity for Hb Zurich-Albisrieden (HBA2: C.178G > C) and the Southeast Asian (- -SEA/) Deletion

Hemoglobin, 2016-09, Vol.40 (5), p.353-355

2016

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Consequences of Delayed Prenatal Diagnosis of β-Thalassemia in Mainland China

Hemoglobin, 2016-05, Vol.40 (3), p.191-193

2016

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Analysis Of δ-Globin Gene Mutations in the Chinese Population

Hemoglobin, 2013-01, Vol.37 (1), p.85-93

2013

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Case Report: Prenatal Diagnosis of Hb Hammersmith [β42(CD1)Phe→Ser; HBB: c.128T > C] in a Family with an Adult Male Patient

Hemoglobin, 2014-01, Vol.38 (2), p.142-145

2014

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A New δ-Globin Gene Variant: Hb A2-Fengshun [δ121(GH4)Glu→Lys (HBD: c.364G > A)]

Hemoglobin, 2016-06, Vol.40 (3), p.213-214

2016

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novel mutation of -50 (G[rightward arrow]A) in the direct repeat element of the β-globin gene identified in a patient with severe β-thalassemia

Annals of hematology, 2009-11, Vol.88 (11), p.1149-1150

2009

Volltextzugriff (PDF)

A Novel Frameshift Mutation at Codons 138/139 (HBB: c.417_418insT) on the β-Globin Gene Leads to β-Thalassemia

Hemoglobin, 2017-01, Vol.41 (1), p.59-60

2017

Volltextzugriff (PDF)

Newborn screening for α-thalassaemia by a capillary electrophoresis method

Journal of medical screening, 2012-09, Vol.19 (3), p.159-159

2012

Volltextzugriff (PDF)

Newborn Screening for Hb H Disease by Determination of Hb Bart's Using the Sebia Capillary Electrophoresis System in Southern China

Hemoglobin, 2014-01, Vol.38 (1), p.73-75

2014

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KLF1 Gene Mutations in Chinese Adults with Increased Fetal Hemoglobin

Hemoglobin, 2013-01, Vol.37 (5), p.501-506

2013

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A New Hemoglobin Variant: Hb Henan [β90(F6)Glu → Gln; HBB: c.271G < C]

Hemoglobin, 2014-01, Vol.38 (2), p.127-129

2014

Volltextzugriff (PDF)

Implementation of Newborn Screening for Hemoglobin H Disease in Mainland China

Indian journal of hematology & blood transfusion, 2015-06, Vol.31 (2), p.242-246

2015

Volltextzugriff (PDF)

Screening for Hb Constant Spring in the Guangdong Province, South China, Using the Sebia Capillary Electrophoresis System

Hemoglobin, 2011-02, Vol.35 (1), p.87-90

2011

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Detection of Hb Constant Spring by a Capillary Electrophoresis Method

Hemoglobin, 2010-04, Vol.34 (2), p.175-178

2010

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Screening for mutations in the α-globin genes leading to abnormal hemoglobin variants with high resolution melting analysis

Clinical chemistry and laboratory medicine, 2012-02, Vol.50 (2), p.273-277

2012

Volltextzugriff (PDF)

Mild hemoglobin H-constant spring disease with β-thalassemia—a case report

Annals of hematology, 2011, Vol.90 (1), p.123-124

2011

Volltextzugriff (PDF)

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Role of Fetal Blood Sampling in the Prenatal Diagnosis of Thalassemia

Prenatal control of nondeletional α-thalassemia: first experience in mainland China

Apparent germline mosaicism for a 15q11-q13 deletion causing recurrent Angelman syndrome in a Chinese family

Co-inheritance of α-thalassaemia and β-thalassaemia in a prenatal screening population in mainland China

Pre Gestational Thalassemia Screening in Mainland China: The First Two Years of a Preventive Program

Pathologic evaluation of uterine leiomyoma treated with radiofrequency ablation

A Krüppel-Like Factor 1 Gene Mutation Ameliorates the Severity of β-Thalassemia: A Case Report

Evidence of Selection for the α-Globin Gene Deletions and Triplications in a Southern Chinese Population

Hb Hornchurch [β43(CD2)Glu→Lys; HBB: c.130G>A] Compromises the Molecular Diagnosis of β-Thalassemia in a Chinese Family

Hydrops Fetalis Associated with Compound Heterozygosity for Hb Zurich-Albisrieden (HBA2: C.178G > C) and the Southeast Asian (- -SEA/) Deletion

Consequences of Delayed Prenatal Diagnosis of β-Thalassemia in Mainland China

Analysis Of δ-Globin Gene Mutations in the Chinese Population

Case Report: Prenatal Diagnosis of Hb Hammersmith [β42(CD1)Phe→Ser; HBB: c.128T > C] in a Family with an Adult Male Patient

A New δ-Globin Gene Variant: Hb A2-Fengshun [δ121(GH4)Glu→Lys (HBD: c.364G > A)]

novel mutation of -50 (G[rightward arrow]A) in the direct repeat element of the β-globin gene identified in a patient with severe β-thalassemia

A Novel Frameshift Mutation at Codons 138/139 (HBB: c.417_418insT) on the β-Globin Gene Leads to β-Thalassemia

Newborn screening for α-thalassaemia by a capillary electrophoresis method

Newborn Screening for Hb H Disease by Determination of Hb Bart's Using the Sebia Capillary Electrophoresis System in Southern China

KLF1 Gene Mutations in Chinese Adults with Increased Fetal Hemoglobin

A New Hemoglobin Variant: Hb Henan [β90(F6)Glu → Gln; HBB: c.271G < C]

Implementation of Newborn Screening for Hemoglobin H Disease in Mainland China

Screening for Hb Constant Spring in the Guangdong Province, South China, Using the Sebia Capillary Electrophoresis System

Detection of Hb Constant Spring by a Capillary Electrophoresis Method

Screening for mutations in the α-globin genes leading to abnormal hemoglobin variants with high resolution melting analysis

Mild hemoglobin H-constant spring disease with β-thalassemia—a case report

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