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International Journal of Hematology, ISSN 0925-5710, 10/2018, Volume 108, Issue 4, pp. 384 - 389
Genotypes of 260 individuals with hemoglobin H (Hb H) disease originating from various provinces in southern Thailand were characterized by multiplex PCR... 
Oncology | Southern Thailand | Hb H disease | Medicine & Public Health | Hematology | Molecular | THALASSEMIA POINT MUTATIONS | DIAGNOSIS | DETERMINANTS | ALPHA-THALASSEMIA | PREVALENCE | COMMON ALPHA | BETA-THALASSEMIA | HEMATOLOGY | RAPID DETECTION | PCR | NORTHERN THAILAND | Hemoglobin | Genotypes | Mutation | Hybridization
Journal Article
Journal of Clinical Laboratory Analysis, ISSN 0887-8013, 09/2019, Volume 33, Issue 7, pp. e22949 - n/a
Journal Article
Hemoglobin, ISSN 0363-0269, 01/2019, Volume 43, Issue 1, pp. 69 - 72
The α + -thal deletion of 3.557 kb (NG_000006.1: g.32745_36301del, -α MAL3.5 ), involving the entire α2-globin gene, was identified in a Chinese family by... 
α-Globin gene cluster | Hb H disease | MAL3.5 | α-thalassemia (α-thal)
Journal Article
by Li, YQ and Liang, L and Tian, M and Qin, T and Wu, X
JOURNAL OF CLINICAL LABORATORY ANALYSIS, ISSN 0887-8013, 09/2019, Volume 33, Issue 7
Background Hb H disease is a serious type of alpha-thalassemia which cause moderate anemia while misdiagnosis by routine genetic analysis in a rare or novel Hb... 
thalassemia | GENE | novel mutation | Hb H disease | MEDICAL LABORATORY TECHNOLOGY | capillary electrophoresis
Journal Article
by Zhao, Y and Lou, JW and Sun, MN and Fu, YQ and Ye, WL and Li, YJ and Dai, YS and Liu, YH
HEMOGLOBIN, ISSN 0363-0269, 01/2019, Volume 43, Issue 1, pp. 69 - 72
The alpha(+)-thal deletion of 3.557kb (NG_000006.1: g.32745_36301del, -alpha(MAL3.5)), involving the entire alpha 2-globin gene, was identified in a Chinese... 
BIOCHEMISTRY & MOLECULAR BIOLOGY | THALASSEMIA | ALPHA | Hb H disease | alpha(MAL3) | HEMATOLOGY | alpha-Globin gene cluster | alpha-thalassemia (alpha-thal)
Journal Article
Hemoglobin, ISSN 0363-0269, 05/2017, Volume 41, Issue 3, pp. 189 - 192
Thalassemia is the most common monogenic disease, with the highest incidence in Guangxi Zhuang Autonomous Region, People's Republic of China (PRC). The blood... 
Hb H disease | α-Thalassemia (α-thal) | multiple mutations | polyadenylation (poly A) signal site | Gene Frequency | Humans | Erythrocyte Indices | Genotype | Poly A - genetics | Sequence Analysis, DNA | Codon | alpha-Globins - genetics | Alleles | Polyadenylation | Hemoglobin H - genetics | alpha-Thalassemia - diagnosis | Adult | Female | Mutation | alpha-Thalassemia - genetics
Journal Article
Clinical Laboratory, ISSN 1433-6510, 2018, Volume 64, Issue 3, pp. 371 - 374
Hb H disease is a form of α-thalassemia. The high clinical variability is influenced by the exact combination of mutations. Here we report on a 29-year-old... 
α-thalassemia | Genetics | Hb H disease
Journal Article
Hemoglobin, ISSN 0363-0269, 11/2018, Volume 42, Issue 5-6, pp. 306 - 309
The aim of this study was to determine the hematological characteristics in a large group of Hb H (beta 4) patients with or without a coexisting... 
genetic association | β-thalassemia (β-thal) | Hb H disease | α-Thalassemia (α-thal) | DIAGNOSIS | POPULATION | ALPHA-THALASSEMIA | BIOCHEMISTRY & MOLECULAR BIOLOGY | DELTA-GLOBIN GENE | IDENTIFICATION | alpha-Thalassemia (alpha-thal) | REVERSE DOT-BLOT | beta-thalassemia (beta-thal) | SPECTRUM | HEMATOLOGY
Journal Article
Hemoglobin, ISSN 0363-0269, 11/2017, Volume 41, Issue 4-6, pp. 293 - 296
Hb H disease is generally a moderate form of α-thalassemia (α-thal) that rarely requires regular blood transfusions. In this study, two Chinese families with... 
HBA1 | transfusion-dependent Hb H disease | Hb Zürich-Albisrieden | Hb Sichuan
Journal Article
Journal Article
HEMOGLOBIN, ISSN 0363-0269, 2017, Volume 41, Issue 4-6, pp. 293 - 296
Hb H disease is generally a moderate form of alpha-thalassemia (alpha-thal) that rarely requires regular blood transfusions. In this study, two Chinese... 
ZURICH-ALBISRIEDEN | HYDROPS-FETALIS | ADANA | Hb Zurich-Albisrieden | transfusion-dependent Hb H disease | ALPHA-THALASSEMIA | BIOCHEMISTRY & MOLECULAR BIOLOGY | Hb Sichuan | HBA1 | HEMATOLOGY | VARIANT | DELETION
Journal Article
Hemoglobin, ISSN 0363-0269, 2019, Volume 42, Issue 5-6, pp. 336 - 338
Hb D-Los Angeles (or Hb D-Punjab) (HBB: c.364G > C) is found worldwide and is derived from a point mutation in the beta-globin gene prevalent in the Punjab... 
α-Thalassemia (α-thal) | Hb D-Los Angeles (HBB: c.364G>C) | MOLECULAR CHARACTERIZATION | HEMOGLOBIN-D | BIOCHEMISTRY & MOLECULAR BIOLOGY | HEMATOLOGY | alpha-Thalassemia (alpha-thal) | HETEROZYGOSITY | PUNJAB BETA-THALASSEMIA | FAMILY
Journal Article
Hemoglobin, ISSN 0363-0269, 2/2014, Volume 38, Issue 1, pp. 76 - 78
Journal Article
Hemoglobin, ISSN 0363-0269, 03/2018, Volume 42, Issue 2, pp. 122 - 125
The choice of acceptor splice site during exon-exon splicing by the spliceosome is determined by a variety of factors. We report here a family with a novel... 
mutation | Hb H disease | Acceptor splice site | α-globin gene | RNA splicing | RNA Splice Sites - genetics | alpha-Globins - genetics | Gene Deletion | Hemoglobins, Abnormal - genetics | Humans | RNA, Messenger - genetics | Child, Preschool | Female | Mutation | alpha-Thalassemia - genetics
Journal Article
by Zhang, Q and Fan, X and Xu, ML and Zhang, YJ and Xu, HL and Wen, XJ and Zhou, WJ
HEMOGLOBIN, ISSN 0363-0269, 2017, Volume 41, Issue 3, pp. 189 - 192
Thalassemia is the most common monogenic disease, with the highest incidence in Guangxi Zhuang Autonomous Region, People's Republic of China (PRC). The blood... 
SOUTHERN CHINA | DIAGNOSIS | BIOCHEMISTRY & MOLECULAR BIOLOGY | Hb H disease | THALASSEMIA MUTATIONS | alpha-Thalassemia (alpha-thal) | multiple mutations | polyadenylation (poly A) signal site | ALPHA-THALASSEMIA-1 | REGION | PROVINCE | SPECTRUM | HEMATOLOGY
Journal Article
HEMOGLOBIN, ISSN 0363-0269, 2018, Volume 42, Issue 2, pp. 122 - 125
The choice of acceptor splice site during exon-exon splicing by the spliceosome is determined by a variety of factors. We report here a family with a novel... 
mutation | Acceptor splice site | ALPHA-THALASSEMIA | BIOCHEMISTRY & MOLECULAR BIOLOGY | CATALYTIC STEP | Hb H disease | HEMATOLOGY | globin gene | RNA splicing
Journal Article
by He, XH and Zhang, R and Mai, GX and Ren, LR and Li, DZ
HEMOGLOBIN, ISSN 0363-0269, 11/2018, Volume 42, Issue 5-6, pp. 344 - 346
In this report, we describe a prenatal case with cardiomegaly and increased middle cerebral artery-peak systolic velocity (MCA-PSV) at 22 weeks' gestation.... 
nondeletional Hb H disease | BIOCHEMISTRY & MOLECULAR BIOLOGY | THALASSEMIA | MUTATION | fetal anemia | HEMATOLOGY | alpha-Thalassemia (alpha-thal) | DELETION
Journal Article
Hemoglobin, ISSN 0363-0269, 11/2018, Volume 42, Issue 5-6, pp. 344 - 346
In this report, we describe a prenatal case with cardiomegaly and increased middle cerebral artery-peak systolic velocity (MCA-PSV) at 22 weeks' gestation.... 
α-Thalassemia (α-thal) | fetal anemia | nondeletional Hb H disease
Journal Article
Hemoglobin, ISSN 0363-0269, 05/2017, Volume 41, Issue 3, pp. 209 - 212
Hb Helsinki [HBB: c.248A>T; β82(EF6)Lys→Met] is a high oxygen affinity hemoglobin (Hb) causing polycythemia, whereas Hb H (β4) disease causes mild to severe... 
high oxygen affinity | Diagnosis | Hb H disease | electrophoresis | Hb Helsinki | Humans | Middle Aged | Genotype | Male | beta-Globins - genetics | Inheritance Patterns | DNA Mutational Analysis | Hemoglobins, Abnormal - genetics | Alleles | alpha-Thalassemia - diagnosis | Mutation | alpha-Thalassemia - genetics | Amino Acid Substitution
Journal Article
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