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Detection of common deletional α‐thalassemia‐2 determinants by PCR

American journal of hematology, 1994-07, Vol.46 (3), p.208-213

1994

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The limitation of genetic testing in diagnosing patients suspected for congenital platelet defects

American journal of hematology, 2020-01, Vol.95 (1), p.E26-E28

2020

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Low pulse oximeter‐measured hemoglobin oxygen saturations with hemoglobin Cheverly

American journal of hematology, 1998-11, Vol.59 (3), p.181-184

1998

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Gamma chain abnormal human fetal hemoglobin variants

American journal of hematology, 1997-07, Vol.55 (3), p.159-163

Huisman, T.H.J.

1997

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Variability in the fetal hemoglobin level of the normal adult

American journal of hematology, 1996-10, Vol.53 (2), p.59-65

1996

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mRNA analysis in reticulocytes of subjects with Hb D, Hb Porto Alegre, Hb E, and different types of unstable hemoglobin variants

American journal of hematology, 1996-08, Vol.52 (4), p.258-263

1996

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Molecular characterization of Hb S(C) β‐thalassemia in American blacks

American journal of hematology, 1991-09, Vol.38 (1), p.9-14

1991

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Polymorphic pattern of the (AT)x(T)y motif at −530 5′ to the β‐globin gene in over 40 patients homozygous for various β‐thalassemia mutations

American journal of hematology, 1994-01, Vol.45 (1), p.51-57

1994

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Isobutyramide therapy in patients with sickle cell anemia

American journal of hematology, 1995-07, Vol.49 (3), p.244-246

1995

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A new α‐thalassemia‐2 deletion resulting in microcytosis and hypochromia and in vitro chain imbalance in the heterozygote

American journal of hematology, 1993-06, Vol.43 (2), p.144-145

1993

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Black β‐thalassemia homozygotes with specific sequence variations in the 5′ hypersensitive site‐2 of the locus control region have high levels of fetal hemoglobin

American journal of hematology, 1992-10, Vol.41 (2), p.97-101

1992

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A novel α‐thalassemia‐2 (−2.7‐kb) observed in a chinese patient with Hb H disease

American journal of hematology, 1991-11, Vol.38 (3), p.248-249

1991

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Clinical, hematological, and molecular features in sicilians with Hb S‐β‐thalassemia

American journal of hematology, 1992-12, Vol.41 (4), p.264-269

1992

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Hb adana or α259(E8)Gly→Aspβ2, A severely unstable α1‐globin variant, observed in combination with the ‐(α)20.5 KB α‐thal‐1 deletion in two Turkish patients

American journal of hematology, 1993-12, Vol.44 (4), p.270-275

1993

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Genetic heterogeneity of β‐thalassemia in southeast sicily

American journal of hematology, 1995-01, Vol.48 (1), p.5-11

1995

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Compound heterozygosity for two α‐globin gene defects, Hb taybe (α1; 38 or 39 minus thr) and a poly a mutation (α2; AATAAA → AATAAG), results in a severe hemolytic anemia

American journal of hematology, 1994-11, Vol.47 (3), p.198-202

1994

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A mild type of Hb S‐β+‐thalassemia [‐92(C→T)] in a sicilian family

American journal of hematology, 1993-02, Vol.42 (2), p.225-226

1993

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Two different mutations in codon 68 are observed in Hb G‐Philadelphia heterozygotes

American journal of hematology, 1994-04, Vol.45 (4), p.345-346

1994

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Spleen in sickle cell anemia: Comparative studies of Nigerian and U.S. patients

American journal of hematology, 1993-03, Vol.42 (3), p.316-321

1993

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Hb lulu island (α2β2107[G9]Gly→Asp)‐β°‐thalassemia (codon 15; TGG → TAG), a form of thalassemia intermedia

American journal of hematology, 1995-09, Vol.50 (1), p.26-29

1995

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Quantities of αQ chain variants in heterozygotes with and without a concomitant β‐thalassemia trait

American journal of hematology, 1994-01, Vol.45 (1), p.91-93

1994

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Quantitation of hemoglobin components by high‐performance cation‐exchange liquid chromatography: Its use in diagnosis and in the assessment of cellular distribution of hemoglobin variants

American journal of hematology, 1984-07, Vol.17 (1), p.39-53

1984

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β‐thalassemia alleles and unstable hemoglobin types among russian pediatric patients

American journal of hematology, 1994-08, Vol.46 (4), p.329-332

1994

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Variation in the level of fetal hemoglobin in (δβ)°‐thalassemia heterozygotes with different numbers of α‐globin genes

American journal of hematology, 1990-07, Vol.34 (3), p.230-231

1990

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A new gene deletion involving the α2‐, α1 ‐, and 81‐globin genes in a black family with Hb H disease

American journal of hematology, 1992-04, Vol.39 (4), p.299-303

1992

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Detection of common deletional α‐thalassemia‐2 determinants by PCR

The limitation of genetic testing in diagnosing patients suspected for congenital platelet defects

Low pulse oximeter‐measured hemoglobin oxygen saturations with hemoglobin Cheverly

Gamma chain abnormal human fetal hemoglobin variants

Variability in the fetal hemoglobin level of the normal adult

mRNA analysis in reticulocytes of subjects with Hb D, Hb Porto Alegre, Hb E, and different types of unstable hemoglobin variants

Molecular characterization of Hb S(C) β‐thalassemia in American blacks

Polymorphic pattern of the (AT)x(T)y motif at −530 5′ to the β‐globin gene in over 40 patients homozygous for various β‐thalassemia mutations

Isobutyramide therapy in patients with sickle cell anemia

A new α‐thalassemia‐2 deletion resulting in microcytosis and hypochromia and in vitro chain imbalance in the heterozygote

Black β‐thalassemia homozygotes with specific sequence variations in the 5′ hypersensitive site‐2 of the locus control region have high levels of fetal hemoglobin

A novel α‐thalassemia‐2 (−2.7‐kb) observed in a chinese patient with Hb H disease

Clinical, hematological, and molecular features in sicilians with Hb S‐β‐thalassemia

Hb adana or α259(E8)Gly→Aspβ2, A severely unstable α1‐globin variant, observed in combination with the ‐(α)20.5 KB α‐thal‐1 deletion in two Turkish patients

Genetic heterogeneity of β‐thalassemia in southeast sicily

Compound heterozygosity for two α‐globin gene defects, Hb taybe (α1; 38 or 39 minus thr) and a poly a mutation (α2; AATAAA → AATAAG), results in a severe hemolytic anemia

A mild type of Hb S‐β+‐thalassemia [‐92(C→T)] in a sicilian family

Two different mutations in codon 68 are observed in Hb G‐Philadelphia heterozygotes

Spleen in sickle cell anemia: Comparative studies of Nigerian and U.S. patients

Hb lulu island (α2β2107[G9]Gly→Asp)‐β°‐thalassemia (codon 15; TGG → TAG), a form of thalassemia intermedia

Quantities of αQ chain variants in heterozygotes with and without a concomitant β‐thalassemia trait

Quantitation of hemoglobin components by high‐performance cation‐exchange liquid chromatography: Its use in diagnosis and in the assessment of cellular distribution of hemoglobin variants

β‐thalassemia alleles and unstable hemoglobin types among russian pediatric patients

Variation in the level of fetal hemoglobin in (δβ)°‐thalassemia heterozygotes with different numbers of α‐globin genes

A new gene deletion involving the α2‐, α1 ‐, and 81‐globin genes in a black family with Hb H disease

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