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Article

Loh at 16p 13 is a novel chromosomal alteration detected in benign and malignant microdissected papillary neoplasms of the breast

1 Oct 1998

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 9781650
DOI: 10.1016/s0046-8177(98)90422-1

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Loh at 16p 13 is a novel chromosomal alteration detected in benign and malignant microdissected papillary neoplasms of the breastPMID 9781650Read ↗

Loss of heterozygosity is detected at chromosomes 1p35-36 (NB), 3p25 (VHL), 16p13 (TSC2/PKD1), and 17p13 (TP53) in microdissected apocrine carcinomas of the breast.Semantic proximity Read ↗

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Genome-wide analysis of DNA copy number changes and LOH in CLL using high-density SNP arrays.Semantic proximity Read ↗

Partial allelotype of carcinoma in situ of the human bladder.Semantic proximity Read ↗

Integrated genomic profiling of chronic lymphocytic leukemia identifies subtypes of deletion 13q14.Semantic proximity Read ↗

17p13 (TP53) Deletions Are Associated With an Aggressive Phenotype but Unrelated to Patient Prognosis in Urothelial Bladder Carcinomas.Semantic proximity Read ↗

Integrative genomics analyses reveal molecularly distinct subgroups of B-cell chronic lymphocytic leukemia patients with 13q14 deletion.Semantic proximity Read ↗

Genetic alterations in ?normal? luminal and myoepithelial cells of the breastSemantic proximity Read ↗

Evaluation of 13q14 status in multiple myeloma by digital single nucleotide polymorphism technology.Semantic proximity Read ↗

An 800-kb region of deletion at 13q14 in human prostate and other carcinomas.Semantic proximity Read ↗

Molecular genetic changes in human epithelial ovarian malignancies.Semantic proximity Read ↗

Gene expression and single nucleotide polymorphism array analyses of spindle cell lipomas and conventional lipomas with 13q14 deletion.Semantic proximity Read ↗

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