EVIDENCE FOR MALE X-CHROMOSOMAL MOSAICISM IN X-LINKED AGAMMAGLOBULINEMIA

被引：27

作者：

HENDRIKS, RW

MENSINK, EJBM

KRAAKMAN, MEM

THOMPSON, A

SCHUURMAN, RKB

机构：

[1] LEIDEN STATE UNIV,MED CTR,DEPT IMMUNOBIOL & GENET,2333 AA LEIDEN,NETHERLANDS

[2] LEIDEN STATE UNIV,MED CTR,DEPT IMMUNOHAEMATOL,2333 AA LEIDEN,NETHERLANDS

[3] LEIDEN STATE UNIV,MED CTR,DEPT PEDIAT,2333 AA LEIDEN,NETHERLANDS

来源：

HUMAN GENETICS | 1989年 / 83卷 / 03期

关键词：

D O I：

10.1007/BF00285169

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

引用

页码：267 / 270

页数：4

共 27 条

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[2]

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[6] A PARTIAL DELETION OF THE MUSCULAR-DYSTROPHY GENE TRANSMITTED TWICE BY AN UNAFFECTED MALE [J].

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[7] REPORT OF THE COMMITTEE ON THE GENETIC CONSTITUTION OF THE X-CHROMOSOMES AND Y-CHROMOSOMES [J].

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MANDEL, JL ;

WEISSENBACH, J ;

FELLOUS, M .

CYTOGENETICS AND CELL GENETICS, 1987, 46 (1-4) :277-315

[8] CARRIER DETECTION IN X-LINKED AGAMMAGLOBULINEMIA BY ANALYSIS OF X-CHROMOSOME INACTIVATION [J].

FEARON, ER ;

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CIVIN, CI ;

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[9] MAMMALIAN X-CHROMOSOME INACTIVATION [J].

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ANNUAL REVIEW OF GENETICS, 1983, 17 :155-190

[10]

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