NEONATAL MANIFESTATIONS OF SCHWARTZ-JAMPEL SYNDROME

被引：25

作者：

FARRELL, SA ^{[1
]}

DAVIDSON, RG ^{[1
]}

THORP, P ^{[1
]}

机构：

[1] MCMASTER UNIV,MED CTR,DEPT PEDIAT,HAMILTON L8S 4L8,ONTARIO,CANADA

来源：

AMERICAN JOURNAL OF MEDICAL GENETICS | 1987年 / 27卷 / 04期

关键词：

D O I：

10.1002/ajmg.1320270409

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

引用

页码：799 / 805

页数：7

共 18 条

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[4] SCHWARTZ-JAMPEL SYNDROME - CLINICAL, ELECTROPHYSIOLOGICAL AND HISTOPATHOLOGICAL STUDY OF A SEVERE VARIANT
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[5] CHONDRODYSTROPHIC MYOTONIA (SCHWARTZ-JAMPEL SYNDROME) - REPORT OF A NEW CASE AND FOLLOW-UP OF PATIENTS INITIALLY REPORTED IN 1969
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[J]. AMERICAN JOURNAL OF MEDICAL GENETICS, 1982, 13 (01): : 51 - 56
[6] CASE OF SCHWARTZ-JAMPEL SYNDROME WITH UNUSUAL MUSCLE BIOPSY FINDINGS
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[J]. ANNALS OF NEUROLOGY, 1978, 3 (01) : 93 - 96
[7] FERGUSON SD, 1981, DEV MED CHILD NEUROL, V23, P237
[8] SCHWARTZ-JAMPEL SYNDROME WITH AUTOSOMAL-DOMINANT INHERITANCE
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[J]. EUROPEAN NEUROLOGY, 1982, 21 (03) : 137 - 146
[9] FOWLER WM, 1974, J NEUROL SCI, V22, P127
[10] ORTHOPEDIC ASPECTS OF SCHWARTZ SYNDROME
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[J]. JOURNAL OF BONE AND JOINT SURGERY-AMERICAN VOLUME, 1975, A 57 (04) : 542 - 544

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