PARTIAL SYNDROME OF MYOTONIC-DYSTROPHY - CLINICAL PRESENTATION AND FOLLOW-UP

被引：8

作者：

MATHIEU, J ^{[1
]}

SIMARD, M ^{[1
]}

DEBRAEKELEER, M ^{[1
]}

BOILY, C ^{[1
]}

DESCHENES, A ^{[1
]}

机构：

[1] HOP CHICOUTIMI,DIV OPHTALMOL,CHICOUTIMI G7H 5H6,QUEBEC,CANADA

来源：

CANADIAN JOURNAL OF NEUROLOGICAL SCIENCES | 1989年 / 16卷 / 01期

关键词：

D O I：

10.1017/S0317167100028614

中图分类号：

R74 [神经病学与精神病学];

学科分类号：

摘要：

引用

页码：99 / 103

页数：5

共 12 条

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CARTER, CO ;

SOOTHILL, JF .

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[2]

Edgington E.S., 1980, RANDOMIZATION TESTS

[3]

HARPER PS, 1973, CLIN GENET, V4, P134

[4]

HARPER PS, 1979, MYOTONIC DYSTROPHY, P14

[5]

LABERGE C, 1985, CYTOGENET CELL GENET, V40, P675

[6]

MARCOZ JP, 1978, J GENET HUM, V3, P237

[7] EARLY DETECTION OF DYSTROPHIA MYOTONICA [J].

POLGAR, JG ;

BRADLEY, WG ;

UPTON, ARM ;

ANDERSON, J ;

HOWAT, JML ;

PETITO, F ;

ROBERTS, DF ;

SCOPA, J .

BRAIN, 1972, 95 :761-776

[8] INCOMPLETE MANIFESTATIONS OF MYOTONIC-DYSTROPHY IN A LARGE KINSHIP IN LABRADOR [J].

PRYSEPHILLIPS, W ;

JOHNSON, GJ ;

LARSEN, B .

ANNALS OF NEUROLOGY, 1982, 11 (06) :582-591

[9]

ROSES AD, 1986, ANN NEUROL, V20, P137

[10]

SHAW DJ, 1985, HUM GENET, V70, P271

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