意大利一个家族中的血红蛋白G圣何塞型 - Suppr

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Haemoglobin G St. José in an Italian family.

作者信息

Ricco G, Gallo E, Pich P G, Rossi G, Miniero R, Mazza U

出版信息

Acta Haematol. 1974;52(3):180-8. doi: 10.1159/000208238.

DOI:10.1159/000208238

PMID:4214182

Abstract

摘要

相似文献

Haemoglobin G St. José in an Italian family.

Acta Haematol. 1974;52(3):180-8. doi: 10.1159/000208238.

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引用本文的文献

Hemoglobin G San José [beta 2 7 (A4) Glu to Gly alpha 2], beta thalassemia, and alpha thalassemia in a Sicilian family.

Hum Genet. 1979 Nov;52(2):239-47. doi: 10.1007/BF00271579.

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Haemoglobin G St. José in an Italian family.

作者信息

Ricco G, Gallo E, Pich P G, Rossi G, Miniero R, Mazza U

出版信息

Acta Haematol. 1974;52(3):180-8. doi: 10.1159/000208238.

DOI:10.1159/000208238

PMID:4214182

Abstract

摘要

相似文献

Haemoglobin G St. José in an Italian family.

Acta Haematol. 1974;52(3):180-8. doi: 10.1159/000208238.

Haemoglobin Constant Spring--a chain termination mutant?

Nature. 1971 Dec 10;234(5328):337-40. doi: 10.1038/234337a0.

Haemoglobin Shepherds Bush (beta 74 [E 18] Gly leads to Asp) in an Italian family.

Acta Haematol. 1977;57(2):102-8. doi: 10.1159/000207866.

Hb Volga or alpha 2 beta 2 27(B9)Ala----Asp in an Italian family.

Hemoglobin. 1985;9(1):91-3. doi: 10.3109/03630268508996988.

A case of homozygous haemoglobin Lepore Boston in Iran.

Acta Haematol. 1975;53(1):60-4. doi: 10.1159/000208157.

Haemoglobin North Shore-Caracas beta 134 (H12) valine replaced by glutamic acid.

FEBS Lett. 1977 Aug 15;80(2):261-5. doi: 10.1016/0014-5793(77)80453-5.

Hereditary persistence of foetal haemoglobin associated with a gamma beta fusion variant, haemoglobin Kenya.

Nat New Biol. 1973 Dec 12;246(154):184-6. doi: 10.1038/newbio246184a0.

Haemoglobin Lepore trait: haematological and structural studies on the Italian population.

Br J Haematol. 1979 Aug;42(4):557-65. doi: 10.1111/j.1365-2141.1979.tb01168.x.

Haemoglobin Stanleyville II (alpha75 [EF 7] Asn yeilds Lys) found in France.

Acta Haematol. 1975;53(1):56-9. doi: 10.1159/000208156.

Hemoglobin Constant Spring, and unusual alpha-chain variant involved in the etiology of hemoglobin H disease.

Ann N Y Acad Sci. 1974;232(0):168-78. doi: 10.1111/j.1749-6632.1974.tb20582.x.

引用本文的文献

Hemoglobin G San José [beta 2 7 (A4) Glu to Gly alpha 2], beta thalassemia, and alpha thalassemia in a Sicilian family.

Hum Genet. 1979 Nov;52(2):239-47. doi: 10.1007/BF00271579.