Found: 8
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Two distinct truncated variants of ankyrin associated with hereditary spherocytosis.
- Published in:
- American Journal of Hematology, 1998, v. 58, n. 1, p. 36, doi. 10.1002/(SICI)1096-8652(199805)58:1<36::AID-AJH7>3.0.CO;2-1
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- Article
Ankyrin Bugey: A de novo deletional frameshift variant in exon 6 of the ankyrin gene associated with spherocytosis.
- Published in:
- American Journal of Hematology, 1997, v. 54, n. 3, p. 242, doi. 10.1002/(SICI)1096-8652(199703)54:3<242::AID-AJH11>3.0.CO;2-F
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- Article
Spα<sup>1/65</sup> hereditary elliptocytosis in North Africa.
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- American Journal of Hematology, 1986, v. 23, n. 2, p. 113, doi. 10.1002/ajh.2830230205
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- Article
Thalassemia-like abnormalities of the red cell membrane in hemoglobin E trait and disease.
- Published in:
- American Journal of Hematology, 1984, v. 16, n. 3, p. 207, doi. 10.1002/ajh.2830160302
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- Article
Kinetic alterations of the red cell membrane phosphatase in α- and β-Thalassemia.
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- American Journal of Hematology, 1982, v. 13, n. 4, p. 269, doi. 10.1002/ajh.2830130402
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- Article
β<sup>+</sup>-Thalassemia Intermedia.
- Published in:
- Human Heredity, 1980, v. 30, n. 5, p. 324, doi. 10.1159/000153151
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- Article
Ankyrin Napoli: a de novo deletional frameshift mutation in exon 16 of ankyrin gene (ANK1) associated with spherocytosis.
- Published in:
- British Journal of Haematology, 1996, v. 93, n. 4, p. 828, doi. 10.1046/j.1365-2141.1996.d01-1746.x
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- Article
Reduction of membrane band 7 and activation of volume stimulated (K<sup>+</sup>, Cl<sup>−</sup>)-cotransport in a case of congenital stomatocytosis.
- Published in:
- British Journal of Haematology, 1989, v. 71, n. 1, p. 141, doi. 10.1111/j.1365-2141.1989.tb06288.x
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- Article