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Academic Journal

Identification of Hb Lepore, Hb anti-Lepore, and α-globin gene triplications by long-read single-molecule real-time sequencing.

  • Authors : Xu A; Department of Laboratory Medicine, Peking University Shenzhen Hospital, Shenzhen, China.; Ye Y

Subjects: Hemoglobins, Abnormal*/Hemoglobins, Abnormal*/Hemoglobins, Abnormal*/genetics ; Hemoglobins, Abnormal*/Hemoglobins, Abnormal*/Hemoglobins, Abnormal*/analysis ; Thalassemia*/Thalassemia*/Thalassemia*/genetics

  • Source: American journal of clinical pathology [Am J Clin Pathol] 2024 Apr 03; Vol. 161 (4), pp. 411-417.Publisher: Oxford University Press Country of Publication: England NLM ID: 0370470 Publication Model: Print Cited Medium: Internet ISSN:

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Editorial & Opinion

Misdiagnosis of Hb Bart's disease: prenatal screening and diagnosis of thalassemia in special population.

  • Authors : Gan G; Department of Genetics Laboratory, Women and Children Care Hospital of Guigang, Guigang, Guangxi, P.R. China.; Li Y

Subjects: Hemoglobins, Abnormal*/Hemoglobins, Abnormal*/Hemoglobins, Abnormal*/genetics ; Hemoglobins, Abnormal*/Hemoglobins, Abnormal*/Hemoglobins, Abnormal*/analysis ; Thalassemia*/Thalassemia*/Thalassemia*/diagnosis

  • Source: Clinical chemistry and laboratory medicine [Clin Chem Lab Med] 2023 May 01; Vol. 61 (10), pp. e210-e213. Date of Electronic Publication: 2023 May 01 (Print Publication: Publisher: Walter De Gruyter Country of Publication: Germany NLM ID: 9806306 Publication Model: Electronic-Print Cited Medium: Internet ISSN:

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Academic Journal

Diagnosis and screening of abnormal hemoglobins.

  • Authors : Sani A; School of Sensing Science and Engineering, School of Electronic Information and Electrical Engineering, Shanghai Jiao Tong University, Shanghai, 200240, China.; Idrees Khan M

Subjects: Hemoglobins, Abnormal*/Hemoglobins, Abnormal*/Hemoglobins, Abnormal*/genetics ; Hemoglobins, Abnormal*/Hemoglobins, Abnormal*/Hemoglobins, Abnormal*/analysis ; Hemoglobinopathies*/Hemoglobinopathies*/Hemoglobinopathies*/diagnosis

  • Source: Clinica chimica acta; international journal of clinical chemistry [Clin Chim Acta] 2024 Jan 01; Vol. 552, pp. 117685. Date of Electronic Publication: 2023 Nov 27.Publisher: Elsevier Country of Publication: Netherlands NLM ID: 1302422 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

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Academic Journal

Distribution characteristics and clinical phenotype analyses of hemoglobin variants in the Z region of Central Guangxi, Southern China.

  • Authors : Chen L; Department of Medical Genetics, Liuzhou Key Laboratory of Birth Defects Prevention and Control, Liuzhou Maternity and Child Healthcare Hospital, Liuzhou, People's Republic of China.; Liuzhou Key Laboratory of Reproductive Medicine, Liuzhou, People's Republic of China.

Subjects: Hemoglobins, Abnormal*/Hemoglobins, Abnormal*/Hemoglobins, Abnormal*/genetics ; Hemoglobins, Abnormal*/Hemoglobins, Abnormal*/Hemoglobins, Abnormal*/analysis ; Thalassemia*

  • Source: Hematology (Amsterdam, Netherlands) [Hematology] 2023 Dec; Vol. 28 (1), pp. 2188651.Publisher: Taylor & Francis Country of Publication: England NLM ID: 9708388 Publication Model: Print Cited Medium: Internet ISSN: 1607-8454

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Academic Journal

Hemoglobin variant in disguise.

  • Authors : Higgins V; DynaLIFE Medical Labs, Edmonton, AB, Canada; Department of Laboratory Medicine and Pathology, University of Alberta, Edmonton, AB, Canada. Electronic address: .

Subjects: Hemoglobins, Abnormal*/Hemoglobins, Abnormal*/Hemoglobins, Abnormal*/genetics ; Hemoglobinopathies*/Hemoglobinopathies*/Hemoglobinopathies*/diagnosis ; Hemoglobinopathies*/Hemoglobinopathies*/Hemoglobinopathies*/genetics

  • Source: Clinical biochemistry [Clin Biochem] 2023 Aug; Vol. 118, pp. 110589. Date of Electronic Publication: 2023 May 24.Publisher: Elsevier Science Country of Publication: United States NLM ID: 0133660 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

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Editorial & Opinion

Compound heterozygotes of Hb Constant Spring and Hb Stanleyville II in HbE/β 0 -thalassemia.

  • Authors : Chen L; Department of Clinical Laboratory, People's Hospital of Baise City, Baise, Guangxi Zhuang Autonomous Region, P.R. China.; Liang L

Subjects: Hemoglobins, Abnormal*/Hemoglobins, Abnormal*/Hemoglobins, Abnormal*/genetics ; Thalassemia* ; beta-Thalassemia*/beta-Thalassemia*/beta-Thalassemia*/genetics

  • Source: Clinical chemistry and laboratory medicine [Clin Chem Lab Med] 2021 Apr 07; Vol. 59 (9), pp. e374-e376. Date of Electronic Publication: 2021 Apr 07 (Print Publication: Publisher: Walter De Gruyter Country of Publication: Germany NLM ID: 9806306 Publication Model: Electronic-Print Cited Medium: Internet ISSN:

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Academic Journal

A novel mutation Hb jiangnan[β3(NA3) Leu→Lys, HBB :c.10-_11delinsAA] causing elevated Hb A 2 level.

  • Authors : Liang L; Center for Medical Genetics and Prenatal Diagnosis, People's Hospital of Guangxi Zhuang Autonomous Region, Nanning, Guangxi, People's Republic of China.; Ning S

Subjects: Hemoglobins, Abnormal*/Hemoglobins, Abnormal*/Hemoglobins, Abnormal*/genetics ; Thalassemia*/Thalassemia*/Thalassemia*/genetics; Adult

  • Source: Hematology (Amsterdam, Netherlands) [Hematology] 2022 Dec; Vol. 27 (1), pp. 772-777.Publisher: Taylor & Francis Country of Publication: England NLM ID: 9708388 Publication Model: Print Cited Medium: Internet ISSN: 1607-8454

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Academic Journal

Identification of Three Families Carrying Hb Anti-Lepore Hong Kong Variant in Guangxi, China, and Analysis of Their Hematological Data.

  • Authors : Long J; School of Basic Medical Sciences, Xi'an Jiaotong University Health Science Center, Xi'an, Shanxi Province, People's Republic of China.; Laboratory of Medical Genetics, Qinzhou Maternal and Child Health Care Hospital, Qinzhou, Guangxi Province, People's Republic of China.

Subjects: Hemoglobins, Abnormal*/Hemoglobins, Abnormal*/Hemoglobins, Abnormal*/genetics ; Thalassemia*/Thalassemia*/Thalassemia*/genetics ; Hematology*

  • Source: Hemoglobin [Hemoglobin] 2022 Nov; Vol. 46 (6), pp. 325-329. Date of Electronic Publication: 2023 Jan 11.Publisher: Informa Healthcare Country of Publication: England NLM ID: 7705865 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

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Academic Journal

Micromapping of Thalassemia and Hemoglobinopathies Among Laos, Khmer, Suay and Yer Ethnic Groups Residing in Lower Northeastern Thailand.

  • Authors : Bunthupanich R; Biomedical Sciences Program, College of Medicine and Public Health, Ubon Ratchathani University, Ubon Ratchathani, Thailand.; Karnpean R

Subjects: Ethnicity*/Ethnicity*/Ethnicity*/genetics ; Mutation*; Hemoglobinopathies/Hemoglobinopathies/Hemoglobinopathies/*epidemiology

  • Source: Hemoglobin [Hemoglobin] 2020 May; Vol. 44 (3), pp. 162-167. Date of Electronic Publication: 2020 Jun 26.Publisher: Informa Healthcare Country of Publication: England NLM ID: 7705865 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

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Academic Journal

Homozygous Hemoglobin Lepore: A Rare Condition Seen in a Bangladeshi Family.

  • Authors : Aziz MA; Md Abdul Aziz, Scientific Officer, Department of Biochemistry and Molecular Biology, Dhaka Shishu (Children) Hospital, Dhaka, Bangladesh; E-mail: .

Subjects: Hemoglobins, Abnormal*/Hemoglobins, Abnormal*/Hemoglobins, Abnormal*/analysis ; Hemoglobins, Abnormal*/Hemoglobins, Abnormal*/Hemoglobins, Abnormal*/genetics ; Thalassemia*

  • Source: Mymensingh medical journal : MMJ [Mymensingh Med J] 2021 Oct; Vol. 30 (4), pp. 1172-1176.Publisher: Mymensingh Medical College Country of Publication: Bangladesh NLM ID: 9601799 Publication Model: Print Cited Medium: Internet ISSN:

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  • 1-10 of  2,013 results for ""Thalassemia""