Advances in the identification of molecular markers for bone neoplasia.

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Advances in the identification of molecular markers for bone neoplasia.

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Advances in the identification of molecular markers for bone neoplasia.

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Advances in the identification of molecular markers for bone neoplasia.

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Advances in the identification of molecular markers for bone neoplasia.

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P1476

Advances in the identification of molecular markers for bone neoplasia.

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P2093

Brendan C Dickson

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Rita A Kandel

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P2860

A novel zinc finger gene is fused to EWS in small round cell tumor

Cloning of the putative tumour suppressor gene for hereditary multiple exostoses (EXT1)

USP6 and CDH11 oncogenes identify the neoplastic cell in primary aneurysmal bone cysts and are absent in so-called secondary aneurysmal bone cysts

Genotype-phenotype correlation in hereditary multiple exostoses

EWS-FLI1 fusion transcript structure is an independent determinant of prognosis in Ewing's sarcoma.

The NFATc2 gene is involved in a novel cloned translocation in a Ewing sarcoma variant that couples its function in immunology to oncology

Clonal karyotypic abnormalities of the hereditary multiple exostoses chromosomal loci 8q24.1 (EXT1) and 11p11-12 (EXT2) in patients with sporadic and hereditary osteochondromas

Rearrangement of the COL12A1 and COL4A5 genes in subungual exostosis: molecular cytogenetic delineation of the tumor-specific translocation t(X;6)(q13-14;q22)

The EXT2 multiple exostoses gene defines a family of putative tumour suppressor genes

Syndrome Characterized by Osteitis Fibrosa Disseminata, Areas of Pigmentation and Endocrine Dysfunction, with Precocious Puberty in Females

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429-438

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P31

scholarly article

P356

10.1517/17530059.2010.496849

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P407

English

P433

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P478

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P577

2010-07-15T00:00:00Z

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P698

23496199

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