(Q33196614)

English

High-resolution analysis of genetic events in cancer cells using bacterial artificial chromosome arrays and comparative genome hybridization

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

23 July 2017

1 reference

Europe PubMed Central

High-resolution analysis of genetic events in cancer cells using bacterial artificial chromosome arrays and comparative genome hybridization (English)

1 reference

Europe PubMed Central

PubMed publication ID

23 July 2017

1 reference

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author name string

John K Cowell

1

1 reference

Europe PubMed Central

PubMed publication ID

23 July 2017

Norma J Nowak

2

1 reference

Europe PubMed Central

PubMed publication ID

23 July 2017

publication date

1 January 2003

1 reference

Europe PubMed Central

PubMed publication ID

23 July 2017

Advances in Cancer Research

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Europe PubMed Central

PubMed publication ID

23 July 2017

90

1 reference

Europe PubMed Central

PubMed publication ID

23 July 2017

91-125

1 reference

Europe PubMed Central

PubMed publication ID

23 July 2017

Chromosomal assignment of human YAC clones by fluorescence in situ hybridization: use of single-yeast-colony PCR and multiple labeling

1 reference

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Specific genetic predictors of chemotherapeutic response and survival in patients with anaplastic oligodendrogliomas

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7 January 2021

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Chemical differentiation along metaphase chromosomes

1 reference

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7 January 2021

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Expression of recessive alleles by chromosomal mechanisms in retinoblastoma

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7 January 2021

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Genetic origin of mutations predisposing to retinoblastoma

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Rapid detection of allelic losses in brain tumours using microsatellite repeat markers and high-performance liquid chromatography

1 reference

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Double minutes and homogeneously staining regions: gene amplification in mammalian cells

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One hundred years of retinoblastoma research. From the clinic to the gene and back again

1 reference

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Isolation and characterisation of a panel of cosmids which allows unequivocal identification of chromosome deletions involving the RB1 gene using fluorescence in situ hybridisation

1 reference

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Genetic and cytogenetic analysis of patients showing reduced esterase-D levels and mental retardation from a survey of 500 individuals with retinoblastoma.

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The aniridia-Wilms' tumour association: molecular and genetic analysis of chromosome deletions on the short arm of chromosome 11.

1 reference

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Mutations in the PAX6 gene in patients with hereditary aniridia

1 reference

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Quantitative analysis of high-resolution trypsin-giemsa bands on human prometaphase chromosomes

1 reference

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Klinefelter's syndrome as a model of anomalous cerebral laterality: testing gene dosage in the X chromosome pseudoautosomal region using a DNA microarray.

1 reference

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Comparative genomic hybridization and its application to Wilms' tumorigenesis

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Somatic inactivation of genes on chromosome 13 is a common event in retinoblastoma

1 reference

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Perlman and Wiedemann-Beckwith syndromes: two distinct conditions associated with Wilms' tumour

1 reference

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Prenatal diagnosis of 13q- syndrome in a fetus with holoprosencephaly and thumb agenesis

1 reference

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Building 'validated' mouse models of human cancer

1 reference

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7 January 2021

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Integration of the physical and genetic linkage map for human chromosome 13

1 reference

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Molecular classification of familial non-BRCA1/BRCA2 breast cancer

1 reference

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Detection and mapping of amplified DNA sequences in breast cancer by comparative genomic hybridization

1 reference

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Comparative genomic hybridization for molecular cytogenetic analysis of solid tumors

1 reference

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7 January 2021

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Localization of the 8;13 translocation breakpoint associated with myeloproliferative disease to a 1.5 mbp region of chromosome 13

1 reference

https://api.crossref.org/works/10.1016%2FS0065-230X%2803%2990003-0

7 January 2021

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Mutation and cancer: statistical study of retinoblastoma

1 reference

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Use of whole cosmid cloned genomic sequences for chromosomal localization by non-radioactive in situ hybridization

1 reference

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7 January 2021

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CHROMOSOME DELETION IN A CASE OF RETINOBLASTOMA.

1 reference

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7 January 2021

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Detecting gene copy number fluctuations in tumor cells by microarray analysis of genomic representations

1 reference

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7 January 2021

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Neural tube defects and the 13q deletion syndrome: evidence for a critical region in 13q33-34.

1 reference

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Application of spectral karyotyping to the analysis of the human chromosome complement of interspecies somatic cell hybrids

1 reference

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Clustering of aberrations to specific chromosomes in human neoplasms. IV. A survey of 1,871 cases

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Integration of cytogenetic landmarks into the draft sequence of the human genome

1 reference

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Cytogenetic analysis using quantitative, high-sensitivity, fluorescence hybridization

1 reference

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Fluorescence in situ hybridization with human chromosome-specific libraries: detection of trisomy 21 and translocations of chromosome 4.

1 reference

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Microarray analysis reveals a major direct role of DNA copy number alteration in the transcriptional program of human breast tumors

1 reference

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The critical role of chromosome translocations in human leukemias.

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A rapid banding technique for human chromosomes

1 reference

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Assembly of microarrays for genome-wide measurement of DNA copy number

1 reference

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Fine structure physical mapping of a 1.9 Mb region of chromosome 13q12.

1 reference

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THE CHROMOSOME NUMBER OF MAN

1 reference

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High Resolution of Human Chromosomes

1 reference

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Trisomy for the distal end of the short arm of chromosome 3: a syndrome

1 reference

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Identifiers

10.1016/S0065-230X(03)90003-0

1 reference

Europe PubMed Central

PubMed publication ID

23 July 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

23 July 2017

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