Study of abnormal hemoglobin in Ehime, Japan: Two structural variants of hemoglobin A (Hb I and Hb J iran) and structural and synthetic variants of delta chain
Author:
Publisher
Springer Science and Business Media LLC
Subject
Genetics (clinical)
Link
http://www.nature.com/articles/jhg198431.pdf
Reference42 articles.
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2. Baur, E.W. 1968. Hb α2 Glu β2 (Hb I) in a Caucasian family: Independent mutation or common origin?Humangenetik 6: 368–372.
3. Beale, D. and Lehmann, H. 1965. Abnormal haemoglobins and the genetic code.Nature 207: 259–261.
4. Bernard, R. and Flavell, R.A. 1980. Physical mapping of the globin gene deletion in hereditary persistence of foetal haemoglobin (HPFH).Nucl. Acids Res. 8: 1521–1534.
5. Betke, K. and Kleihauer, E. 1958. Fetaler und bleibender Blutfarbstoff von Erythrozyten und Erythroblasten von menschlichen Fötus und Neugeborenen.Blut 4: 241–249.
Cited by 2 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
1. HB A2Yokoshima, α2δ225(B7)G1→AsP, A new δ Chain Variant Found in a Japanese Family;Hemoglobin;1985-01
2. Hemoglobin A2Honai (α2δ290(F6)GLU—VAL): A new Delta Chain Variant;Hemoglobin;1985-01
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