A CASE OF PURE RED-CELL APLASIA WITH A HIGH-INCIDENCE OF SPONTANEOUS CHROMOSOME BREAKAGE - A POSSIBLE X-RAY SENSITIVE SYNDROME

被引:13
作者
ISKANDAR, O
JAGER, MJ
WILLENZE, R
NATARAJAN, AT
机构
[1] STATE UNIV LEIDEN,SYLVIUS LABS,DEPT RADIAT GENET & CHEM MUTAGENESIS,LEIDEN,NETHERLANDS
[2] ACAD HOSP LEIDEN,DEPT HAEMATOL,LEIDEN,NETHERLANDS
[3] JA COHEN INST RADIAT PATHOL & RADIAT PROTECT,LEIDEN,NETHERLANDS
关键词
D O I
10.1007/BF00290214
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
引用
收藏
页码:337 / 340
页数:4
相关论文
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