LINKAGE STUDIES IN X-LINKED ALPORT SYNDROME

被引：35

作者：

SZPIROTAPIA, S

BOBRIE, G

GUILLOUDBATAILLE, M

HEUERTZ, S

JULIER, C

FREZAL, J

GRUNFELD, JP

HORSCAYLA, MC

机构：

[1] HOP NECKER ENFANTS MALAD, INSERM, U12, UNITE RECH GENET MED, 149 RUE SEVRES, F-75743 PARIS 15, FRANCE

[2] HOP NECKER ENFANTS MALAD, DEPT NEPHROL, F-75743 PARIS 15, FRANCE

[3] INSERM, U155, UNITE RECH GENET EPIDEMIOL, F-75016 PARIS, FRANCE

[4] CHU HENRI MONDOR, INSERM, U91, UNITE RECH GENET MOLEC & HEMATOL, F-94010 CRETEIL, FRANCE

来源：

HUMAN GENETICS | 1988年 / 81卷 / 01期

关键词：

D O I：

10.1007/BF00283736

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

引用

页码：85 / 87

页数：3

共 19 条

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