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Chemical studies of several varieties of Hb M.

作者信息

GERALD P S, EFRON M L

出版信息

Proc Natl Acad Sci U S A. 1961 Nov 15;47(11):1758-67. doi: 10.1073/pnas.47.11.1758.

Abstract
摘要

引用本文的文献

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Symposium: Hæmolytic Anæmias.
Proc R Soc Med. 1965 Jul;58(7):514-6. doi: 10.1177/003591576505800718.
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Structure-function relations of human hemoglobins.
Proc (Bayl Univ Med Cent). 2006 Jul;19(3):239-45. doi: 10.1080/08998280.2006.11928171.
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HUMAN HAEMOGLOBINS.
J Med Genet. 1965 Mar;2(1):48-90. doi: 10.1136/jmg.2.1.48.
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[The globins].
Blut. 1961;7:433-43. doi: 10.1007/BF01636097.
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Relations between mutations and base sequences in the amino acid code.
Proc Natl Acad Sci U S A. 1962 Oct 15;48(10):1809-15. doi: 10.1073/pnas.48.10.1809.

本文引用的文献

1
Human haemoglobin E: the chemical effect of gene mutation.
Nature. 1959 Sep 19;184:870-2. doi: 10.1038/184870a0.
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Studies on an abnormal hemoglobin causing hereditary congenital cyanosis.
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The amino-acid sequence x-ray methods, and its correlation with chemical data.
Nature. 1961 May 20;190:666-70. doi: 10.1038/190666a0.
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An improved method for the fingerprinting of human hemoglobin.
Biochim Biophys Acta. 1961 Apr 1;48:392-6. doi: 10.1016/0006-3002(61)90490-5.
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Four adult haemoglobin types in one person.
Nature. 1961 Feb 11;189:465-7. doi: 10.1038/189465a0.
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Identity of the alpha-chains of adult and foetal human haemoglobins.
Nature. 1959 May 16;183(4672):1373-5. doi: 10.1038/1831373a0.
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Second spectroscopically abnormal methemoglobin associated with hereditary cyanosis.
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