Search Results - "KENDALL, A. G"

Two Novel β-Thalassemia Mutations in the 5’ and 3’ Noncoding Regions of the β-Globin Gene by Cai, Shi-Ping, Eng, Barry, Francombe, William H., Olivieri, Nancy F., Kendall, Alan G., Waye, John S., Chui, David H.K.

“…Two novel β-thalassemia mutations are described. The first mutation, found in an Italian family, is a G→A substitution in nucleotide (nt) +22 relative to the…”
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Molecular characterization of an atypical β-thalassemia caused by a large deletion in the 5'β-globin gene region by POPOVICH, B. W, ROSENBLATT, D. S, KENDALL, A. G, NISHIOKA, Y

“…We describe a Canadian family of Czechoslovakian descent that came to our attention because of an HbA2 percentage approximately twice that of an average case…”
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Clinical importance of the rare erythrocyte antibody anti-Jra by Kendall, A G

“…Alloantibodies to high-frequency antigens create serious problems for a transfusion service. It is obviously important to know the clinical significance of…”
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Warfarin-carbamazepine interaction by Kendall, A G, Boivin, M

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Rapid analysis of labeled globin chains without acetone precipitation or dialysis by high-pressure liquid chromatography and ion-exchange chromatography by Congote, L F, Kendall, A G

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Hemoglobin Kenya, the product of a gamma-beta fusion gene: studies of the family by Kendall, A G, Ojwang, P J, Schroeder, W A, Huisman, T H

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Deletional beta-thalassemia with high Hb A2 by Kendall, A G, Popovich, B W, Rosenblatt, D S, Nishioka, Y

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Radiological changes in haemoglobin SO disease by Kendall, A G, Calder, J F

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Inherited variants of human red cell carbonic anhydrases by Tashian, R E, Kendall, A G, Carter, N D

“…The present state of knowledge concerning the genetic control of human red cell carbonic anhydrases I and II (CA I and CA II) is reviewed. A total of 25…”
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The Kenya haemoglobin by Kendall, A G, Ojwang, P J

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Hemoglobin Variants in Western Kenya by Kendall, A. G., de Leeuw, N. K. M., Ouna, N., Hira, P.

“…The bloods of 1800 western Kenyans were screened for hemoglobin variants by electrophoresis on cellulose acetate. Variants encountered, besides Hb S, included…”
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The blood coagulation and fibrinolytic enzyme systems in healthy adult Africans and Europeans--a comparative study by Barr, R D, Ouna, N, Kendall, A G

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The hemorrhagic diathesis in renal disease (with special reference to acute uremia) by KENDALL, A G, LOWENSTEIN, L, MORGEN, R O

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Generalized Shwartzman reaction due to gram-negative septicemia after abortion: recovery after bilateral cortical necrosis by Mookerjee, B K, Bilefsky, R, Kendall, A G, Dossetor, J B

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Transplants of glandular tissues for the development of tolerance in birds by Kendall, A G, Jerome, F N

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Acute leukaemia in Kenya by Barr, R D, McCulloch, P B, Mehta, S, Kendall, A G

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Hemoglobin Bart's Disease in an Italian Boy: Interaction between α-Thalassemia and Hereditary Persistence of Fetal Hemoglobin by Chui, David H.K, Patterson, Margaret, Dowling, Carol E, Kazazian, Haig H, Kendall, Alan G

“…HEMOGLOBIN is a tetramer consisting of two pairs of globin chains, each of which is associated with a heme group. In adults, the predominant hemoglobin —…”
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Haemoglobinopathies in Kenya by Kendall, A G, Barr, R D

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Erythrocyte Carbonic Anhydrase I: Inherited Deficiency in Humans by Kendall, Alan G., Tashian, Richard E.

“…The virtually complete absence of erythrocyte carbonic anhydrase I is reported in three members of a family from the Greek island of Icaria. Two members with…”
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Acute leukaemia with mastocytosis by Barr, R D, Kendall, A G

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