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Radiation-induced Genomic Instability: Delayed Cytogenetic Aberrations and Apoptosis in Primary Human Bone Marrow Cells

International journal of radiation biology, 1995, Vol.67 (3), p.287-293

1995

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DNA looping in the α-globin locus

Blood cells, molecules, & diseases, 2007-03, Vol.38 (2), p.129-129

2007

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Localization of the human dopamine beta hydroxylase (DBH) gene to chromosome 9q34

Cytogenetics and cell genetics, 1988, Vol.48 (1), p.48

1988

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α-particle-induced chromosomal instability in human bone marrow cells

The Lancet (British edition), 1994-10, Vol.344 (8928), p.987-988

1994

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Genes upregulated during erythroid differentiation occupy common regions of the nucleus which involve multiple transcription factories

Blood cells, molecules, & diseases, 2007-03, Vol.38 (2), p.128-129

2007

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Dissecting the centromere of the human Y chromosome with cloned telomeric DNA

Human molecular genetics, 1994-08, Vol.3 (8), p.1227-1237

1994

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Chromosomal variation in man: A catalog of chromosomal variants and anomalies, 5th edn

Trends in biochemical sciences (Amsterdam. Regular ed.), 1990-01, Vol.15 (1), p.34

Buckle, V.J.

1990

Volltextzugriff (PDF)

Molecular Mapping of Uncharacteristically Small 5q Deletions in Two Patients with the 5q- Syndrome: Delineation of the Critical Region on 5q and Identification of a 5q- Breakpoint

Genomics (San Diego, Calif.), 1994-02, Vol.19 (3), p.425-432

1994

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New methods in cytogenetics

Current opinion in genetics & development, 1994-06, Vol.4 (3), p.374-382

1994

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Targeted breakage of a human chromosome mediated by cloned human telomeric DNA

Nature genetics, 1992-12, Vol.2 (4), p.283-287

1992

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The identification of a third fragile site, FRAXF, in Xq27 — q28 distal to both FRAXA and FRAXE

Human molecular genetics, 1993-02, Vol.2 (2), p.197-200

1993

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Isolation and characterization of an alphoid centromeric repeat family from the human Y chromosome

Journal of molecular biology, 1985-01, Vol.182 (4), p.477-485

1985

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α-Thalassemia Caused by a Large (62 kb) Deletion Upstream of the Human α Globin Gene Cluster

Blood, 1990-07, Vol.76 (1), p.221-227

1990

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Localisation of a dystrophin-related autosomal gene to 6q24 in man, and to mouse chromosome 10 in the region of the dystrophia muscularis (dy) locus

Human genetics, 1990-08, Vol.85 (3), p.324-326

1990

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Loss of Both CSF1R (FMS) Alleles in Patients with Myelodysplasia and a Chromosome 5 Deletion

Proceedings of the National Academy of Sciences - PNAS, 1991-07, Vol.88 (14), p.6176-6180

1991

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Characterization of three de novo derivative chromosomes 16 by reverse chromosome painting and molecular analysis

American journal of human genetics, 1993-05, Vol.52 (5), p.987-997

1993

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X-linked [alpha]-thalassemia/mental retardation (ATR-X) syndrome: Localization to Xq12-q21. 31 by X inactivation and linkage analysis

American journal of human genetics, 1992-11, Vol.51:5

1992

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Chromosome maps of man and mouse, III

Genomics (San Diego, Calif.), 1987-09, Vol.1 (1), p.3-18

1987

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DETECTION OF BREAKPOINTS IN SUBMICROSCOPIC CHROMOSOMAL TRANSLOCATION, ILLUSTRATING AN IMPORTANT MECHANISM FOR GENETIC DISEASE

The Lancet (British edition), 1989-10, Vol.334 (8667), p.819-824

1989

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A YAC contig across the fragile X site defines the region of fragility

Nucleic acids research, 1991-06, Vol.19 (12), p.3283-3288

1991

Volltextzugriff (PDF)

Molecular mapping of uncharacteristically small 5q deletions in two patients with the 5q-syndrome: Delineation of the critical region on 5q and identification of a 5q-breakout

Genomics (San Diego, Calif.), 1994-02, Vol.19:3

1994

Volltextzugriff (PDF)

Characterisation of molecular DNA rearrangements within the Xq12 – q13.1 region, in three patients with X-linked hypohidrotic ectodermal dysplasia (EDA)

Human molecular genetics, 1993-10, Vol.2 (10), p.1679-1685

1993

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A New Translocation, t(l;3) (p36;q21), in Myelodysplastic Disorders

Blood, 1984-08, Vol.64 (2), p.553-555

1984

Volltextzugriff (PDF)

Chromosomal variation in man: A catalog of chromosomal variants and anomalies, 5th edn: by Digamber S. Borgaonkar, Alan R. Liss, 1989. $96.00 (xiix + 803 pages) ISBN 0 8451 4275 5

Trends in Biochemical Sciences, 1990, Vol.15 (1), p.34-34

Buckle, V.J.

1990

Volltextzugriff (PDF)

Localization of the human tyrosine hydroxylase gene to 11p15: gene duplication and evolution of metabolic pathways

Cytogenetics and cell genetics, 1986, Vol.42 (1-2), p.29

1986

Volltextzugriff (PDF)

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Radiation-induced Genomic Instability: Delayed Cytogenetic Aberrations and Apoptosis in Primary Human Bone Marrow Cells

DNA looping in the α-globin locus

Localization of the human dopamine beta hydroxylase (DBH) gene to chromosome 9q34

α-particle-induced chromosomal instability in human bone marrow cells

Genes upregulated during erythroid differentiation occupy common regions of the nucleus which involve multiple transcription factories

Dissecting the centromere of the human Y chromosome with cloned telomeric DNA

Chromosomal variation in man: A catalog of chromosomal variants and anomalies, 5th edn

Molecular Mapping of Uncharacteristically Small 5q Deletions in Two Patients with the 5q- Syndrome: Delineation of the Critical Region on 5q and Identification of a 5q- Breakpoint

New methods in cytogenetics

Targeted breakage of a human chromosome mediated by cloned human telomeric DNA

The identification of a third fragile site, FRAXF, in Xq27 — q28 distal to both FRAXA and FRAXE

Isolation and characterization of an alphoid centromeric repeat family from the human Y chromosome

α-Thalassemia Caused by a Large (62 kb) Deletion Upstream of the Human α Globin Gene Cluster

Localisation of a dystrophin-related autosomal gene to 6q24 in man, and to mouse chromosome 10 in the region of the dystrophia muscularis (dy) locus

Loss of Both CSF1R (FMS) Alleles in Patients with Myelodysplasia and a Chromosome 5 Deletion

Characterization of three de novo derivative chromosomes 16 by reverse chromosome painting and molecular analysis

X-linked [alpha]-thalassemia/mental retardation (ATR-X) syndrome: Localization to Xq12-q21. 31 by X inactivation and linkage analysis

Chromosome maps of man and mouse, III

DETECTION OF BREAKPOINTS IN SUBMICROSCOPIC CHROMOSOMAL TRANSLOCATION, ILLUSTRATING AN IMPORTANT MECHANISM FOR GENETIC DISEASE

A YAC contig across the fragile X site defines the region of fragility

Molecular mapping of uncharacteristically small 5q deletions in two patients with the 5q-syndrome: Delineation of the critical region on 5q and identification of a 5q-breakout

Characterisation of molecular DNA rearrangements within the Xq12 – q13.1 region, in three patients with X-linked hypohidrotic ectodermal dysplasia (EDA)

A New Translocation, t(l;3) (p36;q21), in Myelodysplastic Disorders

Chromosomal variation in man: A catalog of chromosomal variants and anomalies, 5th edn: by Digamber S. Borgaonkar, Alan R. Liss, 1989. $96.00 (xiix + 803 pages) ISBN 0 8451 4275 5

Localization of the human tyrosine hydroxylase gene to 11p15: gene duplication and evolution of metabolic pathways

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