Citations (8)
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Hareram Pandey, Ravi Ranjan, Kanwaljeet Singh, Amit Sharma, Kamal Kishor, Tulika Seth & Renu Saxena. (2018) Contrasting co-inheritance of alpha and beta mutations in delta beta thalassemia and hereditary persistence of fetal hemoglobin: a study from India. Hematology 23:9, pages 692-696.
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A. D. Adekile. (1997) Historical and Anthropological Correlates of βS Haplotypes and α- and β-Thalassemia Alleles in the Arabian Peninsula. Hemoglobin 21:3, pages 281-296.
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J. S. Waye, B. Eng, M. B. Coleman, M. H. Steinberg & B. P. Alter. (1994) δβ-Thalassemia in an African-American: Identification of the deletion endpoints and PCR-Based diagnosis. Hemoglobin 18:6, pages 389-399.
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Articles from other publishers (5)
Sanjay Pandey, Sweta Pandey, Ravi Ranjan, Rahasyamani Mishra, Monica Sharma & Renu Saxena. (2012) Phenotypic Heterogeneity of Asian Indian Inversion Deletions Gγ(Aγδβ)0 Breakpoint A and Breakpoint B. Indian Journal of Clinical Biochemistry 28:1, pages 98-101.
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Vineeta Sharma, Tulika Seth & Renu Saxena. (2008) Clinical and hematological profile of HbE/Gγ(Aγδβ)0 and Gγ(Aγδβ)0/β0 patients. Clinica Chimica Acta 396:1-2, pages 93-94.
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Supan Fucharoen, Sitthichai Panyasai, Satja Surapot, Goonnapa Fucharoen & Kanokwan Sanchaisuriya. (2005)
Compound heterozygote state for
G
γ
A
γ(δβ)°‐thalassemia and hereditary persistence of fetal hemoglobin
. American Journal of Hematology 80:2, pages 119-123.
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Supan Fucharoen, Yutthana Pengjam, Satja Surapot, Goonnapa Fucharoen & Kanokwan Sanchaisuriya. (2002)
Molecular and hematological characterization of HPFH‐6/Indian deletion–inversion
G
γ(
A
γδβ)
0
‐thalassemia and
G
γ(
A
γδβ)
0
‐thalassemia/HbE in Thai patients
. American Journal of Hematology 71:2, pages 109-113.
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Supan Fucharoen, Yutthana Pengjam, Satja Surapot, Goonnapa Fucharoen & Kanokwan Sanchaisuriya. (2001) Molecular characterization of (δβ)°/β°-thalassemia and (δβ)°-thalassemia/hemoglobin E in Thai patients. European Journal of Haematology 67:4, pages 258-262.
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