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An Extensive Analysis of Y-Chromosomal Microsatellite Haplotypes in Globally Dispersed Human Populations

American journal of human genetics, 2001-04, Vol.68 (4), p.990-1018

2001

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Pre-caucasoid and caucasoid genetic features of the Indian population, revealed by mtDNA polymorphisms

American journal of human genetics, 1996-10, Vol.59 (4), p.927-934

1996

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MOLECULAR SPECTRUM OF β-THALASSEMIA IN THE IRANIAN PROVINCE OF HORMOZGAN

Hemoglobin, 2001-01, Vol.25 (1), p.35-43

2001

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Denaturing gradient gel electrophoresis and direct sequencing of PCR amplified genomic DNA: a rapid and reliable diagnostic approach to beta thalassaemia

British journal of haematology, 1990-10, Vol.76 (2), p.269-274

1990

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Haemoglobinopathy analyses in the Netherlands: a report of an in vitro globin chain biosynthesis survey using a rapid, modified method

Clinical and laboratory haematology, 1999-08, Vol.21 (4), p.247-256

1999

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Adult, fetal, and polycystic kidney expression of polycystin, the polycystic kidney disease-1 gene product

Laboratory investigation, 1996-08, Vol.75 (2), p.221

1996

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Phenotype variability of the dominant β-thalassemia induced in four Dutch families by the rare cd121 (G→T) mutation

Annals of hematology, 1998-12, Vol.77 (6), p.249-255

1998

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Different geographic origins of Hb Constant Spring [alpha(2) codon 142 TAA-->CAA]

Haematologica (Roma), 2001-01, Vol.86 (1), p.36

2001

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Two-colour immunocytochemical staining of gamma (γ) and epsilon (ϵ) type haemoglobin in fetal red cells

Prenatal diagnosis, 1998-11, Vol.18 (11), p.1131-1137

1998

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Characterization and comparison of the human and mouse Dist1/α-globin complex reveals a tightly packed multiple gene cluster containing differentially expressed transcription units

Genomics (San Diego, Calif.), 1996-03, Vol.32 (3), p.341-351

1996

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α-Thalassemia in The Netherlands : a heterogeneous spectrum of both deletions and point mutations

Human genetics, 1997-09, Vol.100 (3-4), p.465-471

1997

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Detection of K-ras mutations by denaturing gradient gel electrophoresis (DGGE): a study on pancreatic cancer

Anticancer research, 1992-09, Vol.12 (5), p.1731

1992

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Localization and Characterization of the Mouse α-Globin Locus Control Region

Genomics (San Diego, Calif.), 1994-05, Vol.21 (2), p.431-433

1994

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Hb Malmö [β-97(FG-4)His→Gln] leading to polycythemia in a Dutch family

Annals of hematology, 1996-10, Vol.73 (4), p.183-188

1996

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Rapid identification by denaturing gradient gel electrophoresis of mutations in the γ‐globin gene promoters in non‐deletion type HPFH

British journal of haematology, 1992-04, Vol.80 (4), p.533-538

1992

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Hb Aghia Sophia [α62(E11)Val→0 (α1)], an "In-Frame" Deletion Causing α-Thalassemia

Hemoglobin, 1999, Vol.23 (4), p.317-324

1999

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mtDNA provides the first known marker distinguishing proto-Indians from the other Caucasoids; it probably predates the diversification between Indians and Orientals

Annals of human biology, 1996-03, Vol.23 (2), p.121-126

1996

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α‐Thalassaemia as a result of a novel splice donor site mutation of the α1‐globin gene

British journal of haematology, 2000-09, Vol.110 (3), p.694-698

2000

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The involvement of Alu repeats in recombination events at the α-globin gene cluster : characterization of two α°-thalassaemia deletion breakpoints

Human genetics, 1997-04, Vol.99 (4), p.528-534

1997

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Structure of the mouse 3-methyladenine DNA glycosylase gene and exact localization upstream of the alpha-globin gene cluster on chromosome 11

Mammalian genome, 1995-08, Vol.6 (8), p.499-504

1995

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A novel polyadenylation signal mutation in the α2‐globin gene causing α thalassaemia

British journal of haematology, 1994-05, Vol.87 (1), p.139-143

1994

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Hb Nijkerk: a new mutation at codons 138/139 of the beta-globin gene inducing severe hemolytic anemia in a Dutch girl

Hemoglobin, 1999-05, Vol.23 (2), p.135-144

1999

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Homozygous beta+ thalassaemia owing to a mutation in the cleavage-polyadenylation sequence of the human beta globin gene

Journal of medical genetics, 1991-04, Vol.28 (4), p.252-255

1991

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Haplotype analysis of two new, independent cases of Hb osu-christiansborg

Hemoglobin, 1999, Vol.23 (2), p.193-195

1999

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Rapid detection of the highly polymorphic beta globin framework by denaturing gradient gel electrophoresis

Journal of medical genetics, 1992-08, Vol.29 (8), p.574-577

1992

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An Extensive Analysis of Y-Chromosomal Microsatellite Haplotypes in Globally Dispersed Human Populations

Pre-caucasoid and caucasoid genetic features of the Indian population, revealed by mtDNA polymorphisms

MOLECULAR SPECTRUM OF β-THALASSEMIA IN THE IRANIAN PROVINCE OF HORMOZGAN

Denaturing gradient gel electrophoresis and direct sequencing of PCR amplified genomic DNA: a rapid and reliable diagnostic approach to beta thalassaemia

Haemoglobinopathy analyses in the Netherlands: a report of an in vitro globin chain biosynthesis survey using a rapid, modified method

Adult, fetal, and polycystic kidney expression of polycystin, the polycystic kidney disease-1 gene product

Phenotype variability of the dominant β-thalassemia induced in four Dutch families by the rare cd121 (G→T) mutation

Different geographic origins of Hb Constant Spring [alpha(2) codon 142 TAA-->CAA]

Two-colour immunocytochemical staining of gamma (γ) and epsilon (ϵ) type haemoglobin in fetal red cells

Characterization and comparison of the human and mouse Dist1/α-globin complex reveals a tightly packed multiple gene cluster containing differentially expressed transcription units

α-Thalassemia in The Netherlands : a heterogeneous spectrum of both deletions and point mutations

Detection of K-ras mutations by denaturing gradient gel electrophoresis (DGGE): a study on pancreatic cancer

Localization and Characterization of the Mouse α-Globin Locus Control Region

Hb Malmö [β-97(FG-4)His→Gln] leading to polycythemia in a Dutch family

Rapid identification by denaturing gradient gel electrophoresis of mutations in the γ‐globin gene promoters in non‐deletion type HPFH

Hb Aghia Sophia [α62(E11)Val→0 (α1)], an "In-Frame" Deletion Causing α-Thalassemia

mtDNA provides the first known marker distinguishing proto-Indians from the other Caucasoids; it probably predates the diversification between Indians and Orientals

α‐Thalassaemia as a result of a novel splice donor site mutation of the α1‐globin gene

The involvement of Alu repeats in recombination events at the α-globin gene cluster : characterization of two α°-thalassaemia deletion breakpoints

Structure of the mouse 3-methyladenine DNA glycosylase gene and exact localization upstream of the alpha-globin gene cluster on chromosome 11

A novel polyadenylation signal mutation in the α2‐globin gene causing α thalassaemia

Hb Nijkerk: a new mutation at codons 138/139 of the beta-globin gene inducing severe hemolytic anemia in a Dutch girl

Homozygous beta+ thalassaemia owing to a mutation in the cleavage-polyadenylation sequence of the human beta globin gene

Haplotype analysis of two new, independent cases of Hb osu-christiansborg

Rapid detection of the highly polymorphic beta globin framework by denaturing gradient gel electrophoresis

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