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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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Hemoglobinopathies Affecting Maternal-Fetal Oxygen Gradient During Pregnancy: Molecular, Biochemical and Clinical Studies

American journal of perinatology, 1998-06, Vol.15 (6), p.389-393

1998

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Electronic access to sequence alignments, experimental results, and human mutations as an aid to studying globin gene regulation

Genomics (San Diego, Calif.), 1998-02, Vol.47 (3), p.429-437

1998

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To the Readers of the Journal Hemoglobin

Hemoglobin, 1998, Vol.22 (3), p.iii-iv

Huisman, Titus H. J.

1998

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Combinations of β chain abnormal hemoglobins with each other or with β-thalassemia determinants with known mutations : influence on phenotype

Clinical chemistry (Baltimore, Md.), 1997-10, Vol.43 (10), p.1850-1856

HUISMAN, T. H. J

1997

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Hb Lepore Washington-Boston in two Mexican mestizo families

Revista de investigacion clinica, 1997-05, Vol.49 (3), p.221

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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Identification of several alpha-globin gene variations in a small Laotian family

Acta haematologica, 1995-01, Vol.94 (3), p.144-147

1995

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Sickle cell anemia identified in a multiple-transfused patient through analysis of mRNA with an RT-PCR-based technique

Acta haematologica, 1995, Vol.93 (2-4), p.105-107

1995

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Factors associated with hypochromia and microcytosis among high school students in the southeastern United States

Southern medical journal (Birmingham, Ala.), 1994-11, Vol.87 (11), p.1132-1137

1994

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Haemoglobin Hammersmith precludes monitoring with conventional pulse oximetry

Canadian journal of anesthesia, 1994-10, Vol.41 (10), p.965-968

1994

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Sickle cell anemia, sickle cell β-thalassemia, and thalassemia major in Albania : characterization of mutations

Human genetics, 1994-02, Vol.93 (2), p.182-187

1994

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Binding of nuclear factors to the proximal and distal CACCC motifs of the beta-globin gene promoter: implications for the -101 (C-->T) 'silent' beta-thalassemia mutation

Acta haematologica, 1994, Vol.91 (1), p.16-20

1994

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The T-->C mutation at position +96 of the untranslated region 3' to the terminating codon of the beta-globin gene is a rare polymorphism that does not cause a beta-thalassemia as previously ascribed

Human genetics, 1994-01, Vol.93 (1), p.77-78

1994

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Level of fetal hemoglobin in children with sickle cell anemia: influence of gender, haplotype and alpha-thalassemia-2 trait

Acta haematologica, 1993, Vol.90 (1), p.34-38

1993

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Heterozygosity for the IVS-I-5(G→C) mutation with a G→A change at codon 18 (Val→Met; Hb Baden) in cis and a T→G mutation at codon 126 (Val→Gly; Hb Djonburi) in trans resulting in a thalassemia intermedia

Biochimica et biophysica acta. Molecular basis of disease, 1992-12, Vol.1180 (2), p.173-179

1992

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Molecular characterization of β-thalassemia in Azerbaijan

Human genetics, 1992-12, Vol.90 (4), p.417-419

1992

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Heterogeneity of the hemoglobin of the Ohrid trout (Salmo L. typicus)

Biochemical genetics, 1992-08, Vol.30 (7-8), p.385-399

1992

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Pseudoautosomal repeat displays higher variability in Blacks than in Caucasians

Human genetics, 1992-03, Vol.88 (5), p.573-578

1992

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Molecular characterization of β-thalassemia in Czechoslovakia

Human genetics, 1992-02, Vol.88 (4), p.399-404

1992

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Combinations of three different forms of alpha-thalassemia in a large Indian family from Durban, South Africa: hematological observations

Acta haematologica, 1992, Vol.87 (1-2), p.11-15

1992

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Hb H Disease Caused by a Homozygosity for the AATAAA→ AATAAG Mutation in the Polyadenylation Site of the α2-Globin Gene: Hematological Observations

Acta haematologica, 1992, Vol.88 (2-3), p.82-85

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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Quantities of adult, fetal and embryonic globin chains in the blood of eighteen- to twenty-week-old human fetuses

Journal of chromatography. Biomedical applications, 1991-07, Vol.567 (2), p.359-368

1991

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The linkage of Hb valletta [α2β287 (F3)Thr→Pro] and Hb f-malta-I [α2Gγ2117(G19)His→Arg] in the maltese population

Human genetics, 1991-04, Vol.86 (6), p.591-594

1991

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Low pulse oximeter‐measured hemoglobin oxygen saturations with hemoglobin Cheverly

Hemoglobinopathies Affecting Maternal-Fetal Oxygen Gradient During Pregnancy: Molecular, Biochemical and Clinical Studies

Electronic access to sequence alignments, experimental results, and human mutations as an aid to studying globin gene regulation

To the Readers of the Journal Hemoglobin

Combinations of β chain abnormal hemoglobins with each other or with β-thalassemia determinants with known mutations : influence on phenotype

Hb Lepore Washington-Boston in two Mexican mestizo families

Variability in the fetal hemoglobin level of the normal adult

Identification of several alpha-globin gene variations in a small Laotian family

Sickle cell anemia identified in a multiple-transfused patient through analysis of mRNA with an RT-PCR-based technique

Factors associated with hypochromia and microcytosis among high school students in the southeastern United States

Haemoglobin Hammersmith precludes monitoring with conventional pulse oximetry

Sickle cell anemia, sickle cell β-thalassemia, and thalassemia major in Albania : characterization of mutations

Binding of nuclear factors to the proximal and distal CACCC motifs of the beta-globin gene promoter: implications for the -101 (C-->T) 'silent' beta-thalassemia mutation

The T-->C mutation at position +96 of the untranslated region 3' to the terminating codon of the beta-globin gene is a rare polymorphism that does not cause a beta-thalassemia as previously ascribed

Level of fetal hemoglobin in children with sickle cell anemia: influence of gender, haplotype and alpha-thalassemia-2 trait

Heterozygosity for the IVS-I-5(G→C) mutation with a G→A change at codon 18 (Val→Met; Hb Baden) in cis and a T→G mutation at codon 126 (Val→Gly; Hb Djonburi) in trans resulting in a thalassemia intermedia

Molecular characterization of β-thalassemia in Azerbaijan

Heterogeneity of the hemoglobin of the Ohrid trout (Salmo L. typicus)

Pseudoautosomal repeat displays higher variability in Blacks than in Caucasians

Molecular characterization of β-thalassemia in Czechoslovakia

Combinations of three different forms of alpha-thalassemia in a large Indian family from Durban, South Africa: hematological observations

Hb H Disease Caused by a Homozygosity for the AATAAA→ AATAAG Mutation in the Polyadenylation Site of the α2-Globin Gene: Hematological Observations

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

Quantities of adult, fetal and embryonic globin chains in the blood of eighteen- to twenty-week-old human fetuses

The linkage of Hb valletta [α2β287 (F3)Thr→Pro] and Hb f-malta-I [α2Gγ2117(G19)His→Arg] in the maltese population

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