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HEMOGLOBIN-Q-INDIA (64 (E13) ASP-HIS) AND BETA THALASSEMIA: A CASE REPORT FROM PUNJAB (NORTH INDIA): To the Editor

European journal of haematology, 1988-03, Vol.40 (3), p.281-281

1988

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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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Radioimmunoassay for Abnormal Hemoglobins

Science (American Association for the Advancement of Science), 1977-06, Vol.196 (4296), p.1334-1336

1977

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Molecular analysis of the high-hemoglobin-F phenotype in Saudi Arabian sickle cell anemia

The New England journal of medicine, 1987-01, Vol.316 (5), p.244

1987

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To the Readers of the Journal Hemoglobin

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

Huisman, Titus H. J.

1998

Volltextzugriff (PDF)

Formation of Ferrihæmoglobin of Isolated Human Hæmoglobin Types by Sodium Nitrite

Nature (London), 1963-11, Vol.200 (4909), p.898-899

1963

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Genetic Aspects of Two Different Minor Hæmoglobin Components found in Cord Blood Samples of Negro Babies

Nature (London), 1960-11, Vol.188 (4750), p.589-590

HUISMAN, TITUS H. J

1960

Volltextzugriff (PDF)

Molecular characterization of β-thalassemia in Czechoslovakia

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

1992

Volltextzugriff (PDF)

Usefulness of cation exchange high performance liquid chromatography as a testing procedure

Pediatrics (Evanston), 1989-05, Vol.83 (5 Pt 2), p.849

Huisman, T H

1989

Volltextzugriff (PDF)

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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Identity of the α-Chains of the Minor Human Hæmoglobin Components A 2 and A 2 ′ with the α-Chains of Human Hæmoglobin A and F

Nature (London), 1961-04, Vol.190 (4773), p.357-358

1961

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Difference in Gross Structure of Two Electrophoretically Identical 'Minor' Hæmoglobin Components

Nature (London), 1962-02, Vol.193 (4814), p.489-491

1962

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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

Volltextzugriff (PDF)

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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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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Polymorphisms in the Human Haptoglobin Gene Cluster: Chromosomes with Multiple Haptoglobin-Related (Hpr) Genes

Proceedings of the National Academy of Sciences - PNAS, 1986-10, Vol.83 (19), p.7395-7399

1986

Volltextzugriff (PDF)

Normal fetal hemoglobin levels in the sudden infant death syndrome

The New England journal of medicine, 1989-11, Vol.321 (20), p.1359

1989

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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

Volltextzugriff (PDF)

Introduction

Hemoglobin, 1984-01, Vol.8 (1), p.83-83

Huisman, Titus H. J.

1984

Volltextzugriff (PDF)

Introduction

Hemoglobin, 1984-01, Vol.8 (1), p.83-83

Huisman, Titus H. J.

1984

Volltextzugriff (PDF)

Percentages of abnormal hemoglobins in adults with a heterozygosity for an α‐chain and/or a β‐chain variant

American journal of hematology, 1983-06, Vol.14 (4), p.393-404

Huisman, Titus H. J.

1983

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

The detection of hemoglobin variants by isoelectrofocusing using EDTA-collected and filter paper-dried cord blood specimens

American journal of clinical pathology, 1990-08, Vol.94 (2), p.199-202

1990

Volltextzugriff (PDF)

Detection of a new hybrid ?2 globin gene among American Blacks

Human genetics, 1988-05, Vol.79 (1), p.68-72

1988

Volltextzugriff (PDF)

Hemoglobin St Luke's or α95Arg2 (G2) β2

European journal of biochemistry, 1972-09, Vol.29 (2), p.301-307

1972

Volltextzugriff (PDF)

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HEMOGLOBIN-Q-INDIA (64 (E13) ASP-HIS) AND BETA THALASSEMIA: A CASE REPORT FROM PUNJAB (NORTH INDIA): To the Editor

Low pulse oximeter‐measured hemoglobin oxygen saturations with hemoglobin Cheverly

Radioimmunoassay for Abnormal Hemoglobins

Molecular analysis of the high-hemoglobin-F phenotype in Saudi Arabian sickle cell anemia

To the Readers of the Journal Hemoglobin

Formation of Ferrihæmoglobin of Isolated Human Hæmoglobin Types by Sodium Nitrite

Genetic Aspects of Two Different Minor Hæmoglobin Components found in Cord Blood Samples of Negro Babies

Molecular characterization of β-thalassemia in Czechoslovakia

Usefulness of cation exchange high performance liquid chromatography as a testing procedure

Haemoglobin Hammersmith precludes monitoring with conventional pulse oximetry

Identity of the α-Chains of the Minor Human Hæmoglobin Components A 2 and A 2 ′ with the α-Chains of Human Hæmoglobin A and F

Difference in Gross Structure of Two Electrophoretically Identical 'Minor' Hæmoglobin Components

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

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

Pseudoautosomal repeat displays higher variability in Blacks than in Caucasians

Polymorphisms in the Human Haptoglobin Gene Cluster: Chromosomes with Multiple Haptoglobin-Related (Hpr) Genes

Normal fetal hemoglobin levels in the sudden infant death syndrome

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

Introduction

Introduction

Percentages of abnormal hemoglobins in adults with a heterozygosity for an α‐chain and/or a β‐chain variant

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

The detection of hemoglobin variants by isoelectrofocusing using EDTA-collected and filter paper-dried cord blood specimens

Detection of a new hybrid ?2 globin gene among American Blacks

Hemoglobin St Luke's or α95Arg2 (G2) β2

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