THE ACROCALLOSAL SYNDROME

被引：22

作者：

PHILIP, N

APICELLA, N

LASSMAN, I

AYME, S

MATTEI, JF

GIRAUD, F

机构：

[1] HOP ENFANTS TIMONE,CTR GENET MED,F-13385 MARSEILLE 5,FRANCE

[2] HOP ENFANTS TIMONE,SERV PEDIAT GEN,F-13385 MARSEILLE 5,FRANCE

[3] HOP ENFANTS TIMONE,SERV RADIOL PEDIAT,F-13385 MARSEILLE 5,FRANCE

来源：

关键词：

D O I：

10.1007/BF00442226

中图分类号：

R72 [儿科学];

学科分类号：

100202 ;

摘要：

引用

页码：206 / 208

页数：3

共 10 条

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FONTES, LR
[J]. AMERICAN JOURNAL OF MEDICAL GENETICS, 1985, 22 (01): : 59 - 68
[3] LEGIUS E, 1985, ANN GENET-PARIS, V28, P239
[4] THE ACROCALLOSAL SYNDROME
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[5] DUPLICATION OF HANDS AND FEET, MULTIPLE JOINT DISLOCATIONS, ABSENCE OF CORPUS-CALLOSUM AND HYPSARRHYTHMIA - ACROCALLOSAL SYNDROME
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[6] SCHINZEL A, 1979, HELV PAEDIATR ACTA, V34, P141
[7] HALLUX DUPLICATION, POSTAXIAL POLYDACTYLY, ABSENCE OF THE CORPUS-CALLOSUM, SEVERE MENTAL-RETARDATION, AND ADDITIONAL ANOMALIES IN 2 UNRELATED PATIENTS - A NEW SYNDROME
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SCHMID, W
[J]. AMERICAN JOURNAL OF MEDICAL GENETICS, 1980, 6 (03): : 241 - 249
[8] SCHINZEL A, 1982, HUM GENET, V62, P382, DOI 10.1007/BF00304564
[9] SCHINZEL A, 1986, CLIN GENET, V30, P399
[10] ACROCALLOSAL SYNDROME
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[J]. AMERICAN JOURNAL OF MEDICAL GENETICS, 1982, 12 (02): : 201 - 203