Identification of five rare mutations including a novel frameshift mutation causing β0-thalassemia in Thai patients with β0-thalassemia/hemoglobin E disease

Birth Defects: Original Article Series.

Annals of Internal Medicine · 1971 · 1.4K citations

Medicine, Obstetrics, Pediatrics +14

Diagnosis of Sickle Cell Anemia and β-Thalassemia with Enzymatically Amplified DNA and Nonradioactive Allele-Specific Oligonucleotide Probes

Randall K. Saiki, C. C. Chang, Corey Levenson et al. · New England Journal of Medicine · 1988 · 293 citations

Medicine, Genetics, Molecular Genetics +17

The molecular basis of alpha‐thalassaemia in Thailand.

Pranee Winichagoon, Douglas R. Higgs, S. E. Y. Goodbourn et al. · The EMBO Journal · 1984 · 141 citations · Full text

Medicine, Genetics, Molecular Genetics +8

Molecular Analysis of the High-Hemoglobin-F Phenotype in Saudi Arabian Sickle Cell Anemia

Barbara A. Miller, Nancy F. Olivieri, Mohammed Salameh et al. · New England Journal of Medicine · 1987 · 119 citations

Life Sciences, Genetics, Molecular Genetics +13

Molecular characterization of β‐globin gene mutations in Malay patients with Hb E‐β‐thalassaemia and thalassaemia major

K. G. Yang, F. Kutlar, Elizabeth George et al. · British Journal of Haematology · 1989 · 104 citations

Life Sciences, Genetics, Hematology +11