Hb E/Hb LeporeHollandia in a family from Bangladesh von Waye, John S., Eng, Barry, Patterson, Margaret, Chui, David H. K., Chang, Lebe S., Cogionis, Bessie, Poon, Annette O., Olivieri, Nancy F.

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An α-Globin Gene Initiation Codon Mutation in a Black Family With HbH Disease von Olivieri, Nancy F., Chang, Lebe S., Poon, AnnetteO, Michelson, Alan M., Orkin, Stuart H.

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Hb E/Hb lepore Hollandia in a family from Bangladesh von WAYE, J. S, ENG, B, PATTERSON, M, CHUI, D. H. K, CHANG, L. S, COGIONIS, B, POON, A. O, OLIVIERI, N. F

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AN INITIATION CODON MUTATION IN THE α1 GLOBIN GENE OF A BLACK FAMILY WITH HbH DISEASE von Olivieri, Nancy F, Poon, Annette O, Chang, Lebe S, Michelson, Alan M, Orkin, Stuart H

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Serum creatine kinase and pyruvate kinase in duchenne muscular dystrophy carrier detection von Percy, Maire E., Chang, Lebe S., Murphy, E. Gordon, Oss, Irina, Verellen-Dumoulin, Christine, Thompson, Margaret W.

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Localization of the Carbohydrate Units in a Human Immunoglobulin Light Chain, Protein Sm λ von GARVER, Fred A., KIEFER, Charles R., CHANG, Lebe S., MENDICINO, Joseph, CHANDRASEKARAN, E. V., ISOBE, Takashi, OSSERMAN, Elliott F.

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Creatine kinase isozyme transition in chicks with hereditary muscular dystrophy von Stewart, Patricia A., Percy, Maire E., Chang, Lebe S., Thompson, Margaret W.

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Physicochemical and immunochemical properties of γ1 heavy chain disease protein baz von Smith, Linda L., Barton, Betty P., Garver, Fred A., Chang, Lebe S., McGuire, Byron, Faguet, Guy B., Lutcher, C. Lawrence

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Structural characterization of γ 1-heavy chain disease protein BAZ: Heterogeneity of the constant region von Garver, Fred A., Chang, Lebe S., McGuire, Byron, Smith, Linda L., Barton, Betty P., Faguet, G.B.

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Structural characterization of γ1-heavy chain disease protein BAZ: Heterogeneity of the constant region von Garver, Fred A., Chang, Lebe S., McGuire, Byron, Smith, Linda L., Barton, Betty P., Faguet, G.B.

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Serum myoglobin in Duchenne muscular dystrophy carrier detection: A comparison with creatine kinase and hemopexin using logistic discrimination von Percy, Maire E., Pichora, Geoffrey A., Chang, Lebe S., Manchester, Kathryn E., Andrews, David F., Opitz, John M.

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Elimination of Transfusions Through Induction of Fetal Hemoglobin Synthesis in Cooley's Anemia von OLIVIERI, NANCY F., REES, DAVID C., GINDER, GORDON D., THEIN, SWEE LAY, WAYE, JOHN S., CHANG, LEBE, BRITTENHAM, GARY M., WEATHERALL, DAVID J.

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Valproic acid and augmentation of fetal hemoglobin in individuals with and without sickle cell disease von Selby, R, Nisbet-Brown, E, Basran, R K, Chang, L, Olivieri, N F

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Incomplete removal of labile fraction when measuring hemoglobin A1c with Bio-Rad Variant analyzer von Ellis, G, Chang, L, Cogionis, B, Daneman, D

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Valproic Acid and Augmentation of Fetal Hemoglobin in Individuals With and Without Sickle Cell Disease von Selby, Rita, Nisbet-Brown, Eric, Basran, Raveen K., Chang, Lebe, Olivieri, Nancy F.

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Elimination of Transfusions Through Induction of Fetal Hemoglobin Synthesis in Cooley's Anemiaa von OLIVIERI, NANCY F., REES, DAVID C., GINDER, GORDON D., THEIN, SWEE LAY, WAYE, JOHN S., CHANG, LEBE, BRITTENHAM, GARY M., WEATHERALL, DAVID J.

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IDENTIFICATION OF TWO NEW α-THALASSEMIA MUTATIONS IN EXON 2 OF THE α1-GLOBIN GENE von Waye, John S., Eng, Barry, Patterson, Margaret, Carcao, Manuel D., Chang, Lebe, Olivieri, Nancy F., Chui, David H. K.

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Primary Structure of a Deleted Human Lambda Type Immunoglobulin Light Chain Containing Carbohydrate: Protein Sm λ von Garver, Fred A., Chang, Lebe, Mendicino, Joseph, Isobe, Takashi, Osserman, Elliott F.

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