THE ACROCALLOSAL SYNDROME IN 1ST COUSINS - WIDENING OF THE SPECTRUM OF CLINICAL-FEATURES AND FURTHER SUPPORT FOR AUTOSOMAL RECESSIVE INHERITANCE

被引：27

作者：

SCHINZEL, A

机构：

来源：

关键词：

D O I：

10.1136/jmg.25.5.332

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

引用

页码：332 / 336

页数：5

共 6 条

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[2] THE ACROCALLOSAL SYNDROME
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[3] DUPLICATION OF HANDS AND FEET, MULTIPLE JOINT DISLOCATIONS, ABSENCE OF CORPUS-CALLOSUM AND HYPSARRHYTHMIA - ACROCALLOSAL SYNDROME
SANCHIS, A
CERVERO, L
MARTINEZ, A
VALVERDE, C
[J]. AMERICAN JOURNAL OF MEDICAL GENETICS, 1985, 20 (01): : 123 - 130
[4] SCHINZEL A, 1979, HELV PAEDIATR ACTA, V34, P141
[5] HALLUX DUPLICATION, POSTAXIAL POLYDACTYLY, ABSENCE OF THE CORPUS-CALLOSUM, SEVERE MENTAL-RETARDATION, AND ADDITIONAL ANOMALIES IN 2 UNRELATED PATIENTS - A NEW SYNDROME
SCHINZEL, A
SCHMID, W
[J]. AMERICAN JOURNAL OF MEDICAL GENETICS, 1980, 6 (03): : 241 - 249
[6] SCHINZEL A, 1986, CLIN GENET, V30, P399