Bilateral neonatal Wilms' tumor with B-C chromosomal translocation.
作者信息
Giangiacomo J, Penchansky L, Monteleone P L, Thompson J
出版信息
J Pediatr. 1975 Jan;86(1):98-102. doi: 10.1016/s0022-3476(75)80715-3.
PMID:162957
Abstract
摘要
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1
Bilateral neonatal Wilms' tumor with B-C chromosomal translocation.伴有B-C染色体易位的双侧新生儿肾母细胞瘤。
J Pediatr. 1975 Jan;86(1):98-102. doi: 10.1016/s0022-3476(75)80715-3.
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Telomeric fusions in a Wilms' tumor.肾母细胞瘤中的端粒融合
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Abnormalities of chromosomes 1 and 11 in Wilms' tumor.肾母细胞瘤中1号和11号染色体的异常。
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Unbalanced translocation of chromosome 3p in Wilms' tumor.肾母细胞瘤中3号染色体短臂的不平衡易位。
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[Genetic events and molecular biology of Wilms' tumor].[肾母细胞瘤的遗传事件与分子生物学]
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Fetal renal hamartoma--a benign tumor to be distinguished from Wilms' tumor. Report of 3 cases.
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[Wilms' tumor and congenital malformations].[肾母细胞瘤与先天性畸形]
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引用本文的文献
1
Wilms' tumor, malformative syndrome, mental retardation and de novo constitutional translocation, t(7;13)(q36;q13).肾母细胞瘤、畸形综合征、智力发育迟缓与新发染色体结构改变，t(7;13)(q36;q13)
Eur J Pediatr. 1984 Jan;141(3):175-7. doi: 10.1007/BF00443220.
2
HRAS1-selected chromosome transfer generates markers that colocalize aniridia- and genitourinary dysplasia-associated translocation breakpoints and the Wilms tumor gene within band 11p13.HRAS1 选择的染色体转移产生了与无虹膜和泌尿生殖系统发育异常相关的易位断点以及位于 11p13 带内的威尔姆斯瘤基因共定位的标记。
Proc Natl Acad Sci U S A. 1987 Aug;84(15):5355-9. doi: 10.1073/pnas.84.15.5355.
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