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المؤلفون: Martin H. Steinberg, M Plonczynski, M. B. Coleman, Z H Lu, C M Smith nd, J G Adams rd, A Harrell
المصدر: The Journal of clinical investigation. 95(2)
مصطلحات موضوعية: Hemolytic anemia, Male, Erythrocytes, Glutamine, Hemoglobins, Abnormal, Molecular Sequence Data, Erythrocytes, Abnormal, Biology, medicine.disease_cause, Polymerase Chain Reaction, Methionine, Reticulocyte Count, Leucine, hemic and lymphatic diseases, medicine, Missense mutation, Humans, Point Mutation, Globin, Amino Acid Sequence, DNA Primers, Sequence Tagged Sites, Genetics, Mutation, Polymorphism, Genetic, Base Sequence, Point mutation, beta-Thalassemia, Beta thalassemia, Infant, Valine, General Medicine, medicine.disease, Molecular biology, Globins, Hemoglobinopathy, Female, Hemoglobin, Research Article
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8565ab5db2c660ce4a2f952a6bd510b4Test
https://pubmed.ncbi.nlm.nih.gov/7860732Test -
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المؤلفون: J G Adams rd, M. B. Coleman, F E Cash, Martin H. Steinberg, Stephen A. Liebhaber
المصدر: The Journal of clinical investigation. 80(1)
مصطلحات موضوعية: Genotype, Mutant, Nonsense mutation, Alpha (ethology), Black People, Alpha-thalassemia, Biology, Gene product, Gene mapping, hemic and lymphatic diseases, medicine, Humans, Globin, RNA, Messenger, Cloning, Molecular, Codon, Gene, Aged, Genetics, Aged, 80 and over, Base Sequence, General Medicine, medicine.disease, Globins, Pedigree, Phenotype, Protein Biosynthesis, Mutation, Thalassemia, Female, Research Article
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::81615506c442756cabf2fc0e0d6abb6cTest
https://pubmed.ncbi.nlm.nih.gov/3597771Test