PRENATAL-DIAGNOSIS OF FRIEDREICH ATAXIA

被引：8

作者：

HANAUER, A

FUJITA, R

TROUILLAS, P

TOMMASIDAVENAS, C

AGID, Y

SECK, A

MANDEL, JL

机构：

[1] HOP NEUROL & NEUROCHIRURG P WERTHEIMER,LYONS,FRANCE

[2] FAC MED STRASBOURG,INSERM,U184,MOLEC BIOL & GENET UNIT,F-67085 STRASBOURG,FRANCE

[3] HOP LA PITIE SALPETRIERE,INSERM,U289,F-75651 PARIS 13,FRANCE

来源：

LANCET | 1990年 / 335卷 / 8697期

关键词：

D O I：

10.1016/0140-6736(90)92679-C

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

引用

页码：1102 / 1102

页数：1

共 5 条

[1]

CHAMBERLAIN S, 1989, AM J HUM GENET, V44, P518

[2] MAPPING OF MUTATION CAUSING FRIEDREICHS ATAXIA TO HUMAN CHROMOSOME-9 [J].

CHAMBERLAIN, S ;

SHAW, J ;

ROWLAND, A ;

WALLIS, J ;

SOUTH, S ;

NAKAMURA, Y ;

VONGABAIN, A ;

FARRALL, M ;

WILLIAMSON, R .

NATURE, 1988, 334 (6179) :248-250

[3] CONFIRMATION OF LINKAGE OF FRIEDREICH ATAXIA TO CHROMOSOME-9 AND IDENTIFICATION OF A NEW CLOSELY LINKED MARKER [J].

FUJITA, R ;

AGID, Y ;

TROUILLAS, P ;

SECK, A ;

TOMMASIDAVENAS, C ;

DRIESEL, AJ ;

OLEK, K ;

GRZESCHIK, KH ;

NAKAMURA, Y ;

MANDEL, JL ;

HANAUER, A .

GENOMICS, 1989, 4 (01) :110-111

[4]

FUJITA R, IN PRESS P NATL ACAD

[5] PRENATAL-DIAGNOSIS OF FRIEDREICH ATAXIA [J].

WALLIS, J ;

SHAW, J ;

WILKES, D ;

FARRALL, M ;

WILLIAMSON, R ;

CHAMBERLAIN, S ;

SKARE, JC ;

MILUNSKY, A .

AMERICAN JOURNAL OF MEDICAL GENETICS, 1989, 34 (03) :458-461

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