TRANSLOCATION BREAKPOINT IN T(11-14) IN B-CELL LEUKEMIA IS NOT AT THE RARE FRAGILE SITE AT 11Q13.3

被引：11

作者：

PUSPURS, AH ^{[1
]}

BAKER, E ^{[1
]}

CALLEN, DF ^{[1
]}

FRATINI, A ^{[1
]}

SUTHERLAND, GR ^{[1
]}

机构：

[1] ADELAIDE CHILDRENS HOSP,CYTOGENET UNIT,N ADELAIDE,SA 5006,AUSTRALIA

来源：

CANCER GENETICS AND CYTOGENETICS | 1988年 / 31卷 / 01期

关键词：

D O I：

10.1016/0165-4608(88)90006-4

中图分类号：

R73 [肿瘤学];

学科分类号：

100214 ;

摘要：

引用

页码：25 / 30

页数：6

共 18 条

[1]

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[2]

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[7] LOCALIZATION OF THE HUMAN HAPTOGLOBIN GENES DISTAL TO THE FRAGILE SITE AT 16Q22 USING IN SITU HYBRIDIZATION [J].

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[8] FRAGILE SITES AT 16Q22 ARE NOT AT THE BREAKPOINT OF THE CHROMOSOMAL REARRANGEMENT IN AMMOL [J].

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[9]

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[10] NO STATISTICAL ASSOCIATION BETWEEN COMMON FRAGILE SITES AND NONRANDOM CHROMOSOME BREAKPOINTS IN CANCER-CELLS [J].

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CANCER GENETICS AND CYTOGENETICS, 1988, 31 (01) :9-15

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