Peer Reviewedhttp://deepblue.lib.umich.edu/bitstream/2027.42/73251/1/j.1365-2141.1976.tb00918.x.pd
investigated in heterozygotes and homozygotes for the sickle cell haemoglobin (Hb S). ID the heteroz...
Thesis (Ph.D.)--Boston UniversityPLEASE NOTE: Boston University Libraries did not receive an Authori...
Alpha-thalassaemia is inherited as an autosomal recessive disorder characterised by a microcytic hyp...
a-thalassemia syndromes the production of a-chain of normal hemoglobin is decreased relative to that...
Two unrelated families are reported in which a β-thalassemia trait occurred with a heterozygosity fo...
The proportion of some a chain variants in the peripheral blood of heterozygotes has been a most use...
Hemoglobinopathies, the disorders of hemoglobin structure and synthesis, can be divided into two for...
Hemoglobin (Hb) Grey Lynn is a Hb variant caused by a substitution of Phe for Leu at position 91 of ...
Peer Reviewedhttp://deepblue.lib.umich.edu/bitstream/2027.42/75046/1/j.1749-6632.1965.tb54045.x.pd
Introduction: Interactions of different hemoglobin variants with thalassemia alleles can result in ...
Summary. An investigation was undertaken to find the incidence of a-thalas-saemia in Egypt. Blood wa...
The presence of Hb New York was confirmed in a Chinese family in which affected members have occasio...
A2 fl-thalassemia trait, the synthesis of P-chains of adult hemoglobin in the peripheral blood is ap...
Hb P-Nilotic which is produced by a hybrid of β and δ genes was found in several members of a Sudane...
Summary The haemoglobinopathies refer to a diverse group of inherited disorders characterized by a r...
investigated in heterozygotes and homozygotes for the sickle cell haemoglobin (Hb S). ID the heteroz...
Thesis (Ph.D.)--Boston UniversityPLEASE NOTE: Boston University Libraries did not receive an Authori...
Alpha-thalassaemia is inherited as an autosomal recessive disorder characterised by a microcytic hyp...
a-thalassemia syndromes the production of a-chain of normal hemoglobin is decreased relative to that...
Two unrelated families are reported in which a β-thalassemia trait occurred with a heterozygosity fo...
The proportion of some a chain variants in the peripheral blood of heterozygotes has been a most use...
Hemoglobinopathies, the disorders of hemoglobin structure and synthesis, can be divided into two for...
Hemoglobin (Hb) Grey Lynn is a Hb variant caused by a substitution of Phe for Leu at position 91 of ...
Peer Reviewedhttp://deepblue.lib.umich.edu/bitstream/2027.42/75046/1/j.1749-6632.1965.tb54045.x.pd
Introduction: Interactions of different hemoglobin variants with thalassemia alleles can result in ...
Summary. An investigation was undertaken to find the incidence of a-thalas-saemia in Egypt. Blood wa...
The presence of Hb New York was confirmed in a Chinese family in which affected members have occasio...
A2 fl-thalassemia trait, the synthesis of P-chains of adult hemoglobin in the peripheral blood is ap...
Hb P-Nilotic which is produced by a hybrid of β and δ genes was found in several members of a Sudane...
Summary The haemoglobinopathies refer to a diverse group of inherited disorders characterized by a r...
investigated in heterozygotes and homozygotes for the sickle cell haemoglobin (Hb S). ID the heteroz...
Thesis (Ph.D.)--Boston UniversityPLEASE NOTE: Boston University Libraries did not receive an Authori...
Alpha-thalassaemia is inherited as an autosomal recessive disorder characterised by a microcytic hyp...
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