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Evolution of a Genetic Disease in an Ethnic Isolate: β-Thalassemia in the Jews of Kurdistan

Proceedings of the National Academy of Sciences - PNAS, 1991-01, Vol.88 (1), p.310-314

1991

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Characterization of β-thalassaemia mutations using direct genomic sequencing of amplified single copy DNA

Nature (London), 1987-11, Vol.330 (6146), p.384-386

1987

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Dominant Thalassemia-like Phenotypes Associated With Mutations in Exon 3 of the β-Globin Gene

Blood, 1992-06, Vol.79 (11), p.3014-3018

1992

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Potential influence of a marine heatwave on range extensions of tropical fishes in the eastern Indian Ocean—Invaluable contributions from amateur observers

Regional studies in marine science, 2017-05, Vol.13, p.19-31

2017

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A pseudodeficiency allele common in non-Jewish Tay-Sachs carriers: implications for carrier screening

American journal of human genetics, 1992-10, Vol.51 (4), p.793-801

1992

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Automata for the assessment of knowledge

IEEE transactions on knowledge and data engineering, 2001-05, Vol.13 (3), p.451-461

2001

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The Spectrum of β-Thalassemia Genes in China and Southeast Asia

Blood, 1986-10, Vol.68 (4), p.964-966

1986

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Homozygous β-Thalassemia Without Anemia

Blood, 1989-01, Vol.73 (1), p.324-328

1989

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Characterization of a spontaneous mutation to a β-thalassemia allele

American journal of human genetics, 1986-06, Vol.38 (6), p.860-867

1986

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Hinf I polymorphism 3' to the human β-globin gene detected by the polymerase chain reaction (PCR)

Nucleic acids research, 1989-03, Vol.17 (6), p.2376-2376

1989

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Use of residence-time distribution techniques to analyze industrial-scale froth-flotation circuits

Minerals & metallurgical processing, 1999-02, Vol.16 (1), p.18-26

1999

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On the Irredundant Generation of Knowledge Spaces

Journal of mathematical psychology, 1993-03, Vol.37 (1), p.49-62

Dowling, Cornelia E.

1993

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Applying the Basis of a Knowledge Space for Controlling the Questioning of an Expert

Journal of mathematical psychology, 1993-03, Vol.37 (1), p.21-48

Dowling, Cornelia E.

1993

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Knowledge Structures

Albert, Dietrich

1, 1994

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A RAPID DNA METHOD FOR FIRST‐TRIMESTER PRENATAL DIAGNOSIS

British journal of haematology, 1988-12, Vol.70 (4), p.504-505

1988

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A novel mutation in the invariant AG of the acceptor splice site of intron 4 of the β-hexosaminidase α-subunit gene in two unrelated American black GM2-gangliosidosis (tay-sachs disease) patients

American journal of human genetics, 1991-06, Vol.48 (6), p.1181-1185

1991

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Comparison of deficiency alleles of the beta-globin and factor VIII:C genes: new lessons from a giant gene

Cold Spring Harbor Symposia on Quantitative Biology, 1986, Vol.51 Pt 1, p.371

1986

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β-Thalassemia in China: a Systematic Molecular Characterization of β-Thalassemia Mutations

Hemoglobin, 1988, Vol.12 (5-6), p.621-628

1988

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The spectrum of beta-thalassemia genes in China and Southeast Asia

Blood, 1986-10, Vol.68 (4), p.964-966

1986

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Gene Defects in β-Thalassemia and Their Prenatal Diagnosis

Annals of the New York Academy of Sciences, 1990-12, Vol.612 (1), p.1-14

1990

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Model Discrimination in the Flotation of a Porphyry Copper Ore

Mining, metallurgy & exploration, 1985-05, Vol.2 (2), p.87-101

1985

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Evidence supporting a single origin of the beta(C)-globin gene in blacks

American journal of human genetics, 1985-07, Vol.37 (4), p.771-777

1985

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Hemoglobin Bart's Disease in an Italian Boy: Interaction between α-Thalassemia and Hereditary Persistence of Fetal Hemoglobin

The New England journal of medicine, 1990-07, Vol.323 (3), p.179-182

1990

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The spectrum of β‐thalassaemia mutations in Sicily

British journal of haematology, 1988-07, Vol.69 (3), p.393-397

1988

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Prenatal Diagnosis of Sickle Cell Anemia-1988

Annals of the New York Academy of Sciences, 1989-01, Vol.565 (1), p.44-47

1989

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Evolution of a Genetic Disease in an Ethnic Isolate: β-Thalassemia in the Jews of Kurdistan

Characterization of β-thalassaemia mutations using direct genomic sequencing of amplified single copy DNA

Dominant Thalassemia-like Phenotypes Associated With Mutations in Exon 3 of the β-Globin Gene

Potential influence of a marine heatwave on range extensions of tropical fishes in the eastern Indian Ocean—Invaluable contributions from amateur observers

A pseudodeficiency allele common in non-Jewish Tay-Sachs carriers: implications for carrier screening

Automata for the assessment of knowledge

The Spectrum of β-Thalassemia Genes in China and Southeast Asia

Homozygous β-Thalassemia Without Anemia

Characterization of a spontaneous mutation to a β-thalassemia allele

Hinf I polymorphism 3' to the human β-globin gene detected by the polymerase chain reaction (PCR)

Use of residence-time distribution techniques to analyze industrial-scale froth-flotation circuits

On the Irredundant Generation of Knowledge Spaces

Applying the Basis of a Knowledge Space for Controlling the Questioning of an Expert

Knowledge Structures

A RAPID DNA METHOD FOR FIRST‐TRIMESTER PRENATAL DIAGNOSIS

A novel mutation in the invariant AG of the acceptor splice site of intron 4 of the β-hexosaminidase α-subunit gene in two unrelated American black GM2-gangliosidosis (tay-sachs disease) patients

Comparison of deficiency alleles of the beta-globin and factor VIII:C genes: new lessons from a giant gene

β-Thalassemia in China: a Systematic Molecular Characterization of β-Thalassemia Mutations

The spectrum of beta-thalassemia genes in China and Southeast Asia

Gene Defects in β-Thalassemia and Their Prenatal Diagnosis

Model Discrimination in the Flotation of a Porphyry Copper Ore

Evidence supporting a single origin of the beta(C)-globin gene in blacks

Hemoglobin Bart's Disease in an Italian Boy: Interaction between α-Thalassemia and Hereditary Persistence of Fetal Hemoglobin

The spectrum of β‐thalassaemia mutations in Sicily

Prenatal Diagnosis of Sickle Cell Anemia-1988

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