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Gene expression profiling identifies different sub-types of retinoblastoma

British journal of cancer, 2013-07, Vol.109 (2), p.512-525

2013

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Mutations associated with variant phenotypes in ataxia-telangiectasia

American journal of human genetics, 1996-08, Vol.59 (2), p.320-330

1996

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Neuroblastomas with chromosome 11q loss and single copy MYCN comprise a biologically distinct group of tumours with adverse prognosis

British journal of cancer, 2001-08, Vol.85 (4), p.531-537

2001

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Mutations Revealed by Sequencing the 5′ Half of the Gene for Ataxia Telangiectasia

Human molecular genetics, 1996-01, Vol.5 (1), p.145-149

1996

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Identification and analysis of expression of human VACM-1, a cullin gene family member located on chromosome 11q22-23

Genome research, 1997-01, Vol.7 (1), p.71-75

1997

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Clonal diversity of Ig and T-cell-receptor gene rearrangements identifies a subset of childhood B-precursor acute lymphoblastic leukemia with increased risk of relapse

Blood, 1998-08, Vol.92 (3), p.952-958

1998

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A family showing no evidence of linkage between the ataxia telangiectasia gene and chromosome 11q22-23

Journal of medical genetics, 1993-02, Vol.30 (2), p.135-140

1993

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Genetic and Cellular Features of Ataxia Telangiectasia

International Journal of Radiation Biology [INT. J. RADIAT. BIOL.]. Vol. 65, no. 1. 1994, 1994, Vol.65 (1), p.65-70

1994

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Detection of MYCN Amplification in Neuroblastoma using Competitive PCR Quantitation

Laboratory investigation, 2000-02, Vol.80 (2), p.271-273

2000

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Severe microcephaly with normal intellectual development: the Nijmegen breakage syndrome

Archives of disease in childhood, 1995-11, Vol.73 (5), p.431-434

1995

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Weak linkage at 4p16 to predisposition for human neuroblastoma

Oncogene, 2002-11, Vol.21 (54), p.8356-8360

2002

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Neuroblastoma – a developmental perspective

Cancer letters, 2003-07, Vol.197 (1), p.3-9

2003

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The Order and Orientation of a Cluster of Metalloproteinase Genes, Stromelysin 2, Collagenase, and Stromelysin, Together with D11S385, on Chromosome 11q22-q23

Genomics (San Diego, Calif.), 1993-04, Vol.16 (1), p.289-291

1993

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Analysis of 133 Meioses Places the Genes for Nevoid Basal Cell Carcinoma (Gorlin) Syndrome and Fanconi Anemia Group C in a 2.6-cM Interval and Contributes to the Fine Map of 9q22.3

Genomics (San Diego, Calif.), 1994-09, Vol.23 (2), p.486-489

1994

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Construction of a Transcription Map around the Gene for Ataxia Telangiectasia: Identification of at Least Four Novel Genes

Genomics (San Diego, Calif.), 1997-03, Vol.40 (2), p.267-276

1997

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Analysis of 7 polymorphic markers at chromosome 11q22-23 in 35 ataxia telangiectasia families;further evidence of linkage

Human genetics, 1990-07, Vol.85 (2), p.215-220

1990

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Irradiation Hybrids for Human Chromosome 11: Characterization and Use for Generating Region-Specific Markers in 11q14-q23

Genomics (San Diego, Calif.), 1993-02, Vol.15 (2), p.332-341

1993

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Cancer and DNA processing disorders

British medical bulletin, 1994-07, Vol.50 (3), p.708-717

1994

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A Physical Map across Chromosome 11q22-q23 Containing the Major Locus for Ataxia Telangiectasia

Genomics (San Diego, Calif.), 1994-06, Vol.21 (3), p.612-619

1994

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Molecular analysis of single colonies reveals a diverse origin of initial clonal proliferation in B-precursor acute lymphoblastic leukemia that can precede the t(12;21) translocation

Cancer research (Chicago, Ill.), 2001-12, Vol.61 (23), p.8547-8553

2001

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Paired STSs amplified from radiation hybrids, and from associated YACs, identify highly polymorphic loci flanking the ataxia telangiectasia locus on chromosome 11q22–23

Human molecular genetics, 1993-07, Vol.2 (7), p.969-974

1993

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A Haplotype Common to Intermediate Radiosensitivity Variants of Ataxia-telangiectasia in the UK

International journal of radiation biology, 1994, Vol.66 (6), p.S35-S41

1994

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Genetic and Physical Mapping of the Ataxia-telangiectasia Locus on Chromosome 11q22-q23

International journal of radiation biology, 1994, Vol.66 (6), p.S45-S56

1994

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Clonal Diversity of Ig and T-cell Receptor Gene Rearrangements in Childhood B-Precursor Acute Lymphoblastic Leukaemia

Leukemia & lymphoma, 2000, Vol.36 (3-4), p.213-224

2000

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Fine mapping of the chromosome 11q22-23 region using PFGE, linkage and haplotype analysis ; localization of the gene for ataxia telangiectasia to a 5cM region flanked by NCAM/DRD2 and STMY/CJ52.75, Ø2.22

Nucleic acids research, 1990-08, Vol.18 (15), p.4335-4343

1990

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Gene expression profiling identifies different sub-types of retinoblastoma

Mutations associated with variant phenotypes in ataxia-telangiectasia

Neuroblastomas with chromosome 11q loss and single copy MYCN comprise a biologically distinct group of tumours with adverse prognosis

Mutations Revealed by Sequencing the 5′ Half of the Gene for Ataxia Telangiectasia

Identification and analysis of expression of human VACM-1, a cullin gene family member located on chromosome 11q22-23

Clonal diversity of Ig and T-cell-receptor gene rearrangements identifies a subset of childhood B-precursor acute lymphoblastic leukemia with increased risk of relapse

A family showing no evidence of linkage between the ataxia telangiectasia gene and chromosome 11q22-23

Genetic and Cellular Features of Ataxia Telangiectasia

Detection of MYCN Amplification in Neuroblastoma using Competitive PCR Quantitation

Severe microcephaly with normal intellectual development: the Nijmegen breakage syndrome

Weak linkage at 4p16 to predisposition for human neuroblastoma

Neuroblastoma – a developmental perspective

The Order and Orientation of a Cluster of Metalloproteinase Genes, Stromelysin 2, Collagenase, and Stromelysin, Together with D11S385, on Chromosome 11q22-q23

Analysis of 133 Meioses Places the Genes for Nevoid Basal Cell Carcinoma (Gorlin) Syndrome and Fanconi Anemia Group C in a 2.6-cM Interval and Contributes to the Fine Map of 9q22.3

Construction of a Transcription Map around the Gene for Ataxia Telangiectasia: Identification of at Least Four Novel Genes

Analysis of 7 polymorphic markers at chromosome 11q22-23 in 35 ataxia telangiectasia families;further evidence of linkage

Irradiation Hybrids for Human Chromosome 11: Characterization and Use for Generating Region-Specific Markers in 11q14-q23

Cancer and DNA processing disorders

A Physical Map across Chromosome 11q22-q23 Containing the Major Locus for Ataxia Telangiectasia

Molecular analysis of single colonies reveals a diverse origin of initial clonal proliferation in B-precursor acute lymphoblastic leukemia that can precede the t(12;21) translocation

Paired STSs amplified from radiation hybrids, and from associated YACs, identify highly polymorphic loci flanking the ataxia telangiectasia locus on chromosome 11q22–23

A Haplotype Common to Intermediate Radiosensitivity Variants of Ataxia-telangiectasia in the UK

Genetic and Physical Mapping of the Ataxia-telangiectasia Locus on Chromosome 11q22-q23

Clonal Diversity of Ig and T-cell Receptor Gene Rearrangements in Childhood B-Precursor Acute Lymphoblastic Leukaemia

Fine mapping of the chromosome 11q22-23 region using PFGE, linkage and haplotype analysis ; localization of the gene for ataxia telangiectasia to a 5cM region flanked by NCAM/DRD2 and STMY/CJ52.75, Ø2.22

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