Search Results

Filter
  • 1-10 of  40 results for ""HEMOGLOBIN genetics""
Item request has been placed! ×
Item request cannot be made. ×
loading  Processing Request
Academic Journal

De-novo ATR-16 syndrome associated with inherited hemoglobin Evanston causing HbH phenotype: a rare occurrence.

  • Authors : Jajodia E; Molecular Genetics, Unipath Specialty Laboratory, Ahmedabad, Gujarat, India.; Menghani H

Subjects: alpha-Thalassemia*/alpha-Thalassemia*/alpha-Thalassemia*/genetics ; alpha-Thalassemia*/alpha-Thalassemia*/alpha-Thalassemia*/complications ; Phenotype*

  • Source: Annals of hematology [Ann Hematol] 2024 Sep; Vol. 103 (9), pp. 3805-3810. Date of Electronic Publication: 2024 Jul 11.Publisher: Springer Verlag Country of Publication: Germany NLM ID: 9107334 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

Record details

×
Academic Journal

The role of molecular diagnostic testing for hemoglobinopathies and thalassemias.

  • Authors : Sabath DE; Department of Laboratory Medicine and Pathology, University of Washington, Seattle, Washington, USA.

Subjects: beta-Thalassemia*/beta-Thalassemia*/beta-Thalassemia*/diagnosis ; beta-Thalassemia*/beta-Thalassemia*/beta-Thalassemia*/genetics ; Hemoglobinopathies*/Hemoglobinopathies*/Hemoglobinopathies*/diagnosis

  • Source: International journal of laboratory hematology [Int J Lab Hematol] 2023 Jun; Vol. 45 Suppl 2, pp. 71-78. Date of Electronic Publication: 2023 May 21.Publisher: Blackwell Scientific Publications Country of Publication: England NLM ID: 101300213 Publication Model: Print-Electronic Cited Medium:

Record details

×
Academic Journal

Clinical significance of mutational variants in beta and alpha genes in patients with hemoglobinopathies from two large Greek centers: a complex interplay between genotype and phenotype.

  • Authors : Diamantidis MD; Thalassemia and Sickle Cell Disease Unit, Department of Hematology, First Department of Internal Medicine, General Hospital of Larissa, Tsakalov St. 1, 41 221, Larissa, Greece. .; Karanikola RA

Subjects: Hemoglobinopathies*/Hemoglobinopathies*/Hemoglobinopathies*/genetics ; beta-Thalassemia*/beta-Thalassemia*/beta-Thalassemia*/epidemiology ; beta-Thalassemia*/beta-Thalassemia*/beta-Thalassemia*/genetics

  • Source: Journal of molecular medicine (Berlin, Germany) [J Mol Med (Berl)] 2023 Sep; Vol. 101 (9), pp. 1073-1082. Date of Electronic Publication: 2023 Jul 07.Publisher: Springer International Country of Publication: Germany NLM ID: 9504370 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

Record details

×
Academic Journal

Does size matter? Two new deletions in the HBB gene cause β 0 -thalassemia.

  • Authors : Ropero P; Hematology Service, Hospital Clínico San Carlos, C/Profesor Martín Lagos s/n, 28040, Madrid, Spain. .; Instituto de Investigación Sanitaria Hospital Clínico San Carlos, Madrid, Spain. .

Subjects: alpha-Thalassemia*/alpha-Thalassemia*/alpha-Thalassemia*/genetics ; beta-Thalassemia*/beta-Thalassemia*/beta-Thalassemia*/diagnosis ; beta-Thalassemia*/beta-Thalassemia*/beta-Thalassemia*/genetics

  • Source: Annals of hematology [Ann Hematol] 2022 Jul; Vol. 101 (7), pp. 1465-1471. Date of Electronic Publication: 2022 Apr 25.Publisher: Springer Verlag Country of Publication: Germany NLM ID: 9107334 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

Record details

×
Academic Journal

Early genetic screening uncovered a high prevalence of thalassemia among 18 309 neonates in Guizhou, China.

  • Authors : Tan M; Department of Pediatrics, Affiliated Hospital of Zunyi Medical University, Zunyi, China.; Bai Y

Subjects: Genetic Testing*; alpha-Thalassemia/alpha-Thalassemia/alpha-Thalassemia/*epidemiology ; beta-Thalassemia/beta-Thalassemia/beta-Thalassemia/*epidemiology

  • Source: Clinical genetics [Clin Genet] 2021 May; Vol. 99 (5), pp. 704-712. Date of Electronic Publication: 2021 Mar 09.Publisher: Munksgaard Country of Publication: Denmark NLM ID: 0253664 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1399-0004

Record details

×
Academic Journal

Newborn Screening Practices and Alpha-Thalassemia Detection - United States, 2016.

Subjects: *HYDROPS fetalis; *NEWBORN screening; *ALPHA-Thalassemia

  • Source: MMWR: Morbidity & Mortality Weekly Report. 9/11/2020, Vol. 69 Issue 36, p1269-1272. 4p.

Record details

×
  • 1-10 of  40 results for ""HEMOGLOBIN genetics""