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Presence or absence of trisomy 11 is correlated with histologic subtype in congenital mesoblastic nephroma.

作者信息

Mascarello J T, Cajulis T R, Krous H F, Carpenter P M

机构信息

Genetic Services, Children's Hospital-San Diego, CA 92123.

出版信息

Cancer Genet Cytogenet. 1994 Oct;77(1):50-4. doi: 10.1016/0165-4608(94)90148-1.

DOI:10.1016/0165-4608(94)90148-1
PMID:7923083
Abstract

Fluorescence in situ hybridization utilizing a probe for the alpha satellite repeat sequence on chromosome 11 was used to detect variations in the number of chromosomes 11 in 24 formalin-fixed, paraffin-embedded congenital mesoblastic nephromas. Evidence of trisomy 11 was found in nearly half of the tumors. More importantly, the presence of trisomy 11 was associated with the cellular histologic variant of this tumor.

摘要

相似文献

1
Presence or absence of trisomy 11 is correlated with histologic subtype in congenital mesoblastic nephroma.
Cancer Genet Cytogenet. 1994 Oct;77(1):50-4. doi: 10.1016/0165-4608(94)90148-1.
2
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引用本文的文献

1
Congenital mesoblastic nephroma t(12;15) is associated with ETV6-NTRK3 gene fusion: cytogenetic and molecular relationship to congenital (infantile) fibrosarcoma.先天性中胚层肾瘤t(12;15)与ETV6-NTRK3基因融合相关：与先天性（婴儿型）纤维肉瘤的细胞遗传学及分子关系
Am J Pathol. 1998 Nov;153(5):1451-8. doi: 10.1016/S0002-9440(10)65732-X.