CONGENITAL ABSENCE OF PYRAMIDS AND ITS SIGNIFICANCE IN GENETIC-DISEASES

被引：41

作者：

CHOW, CW

HALLIDAY, JL

ANDERSON, RM

DANKS, DM

FORTUNE, DW

机构：

[1] ROYAL CHILDRENS HOSP,BIRTH DEFECTS RES INST,PARKVILLE,VIC 3052,AUSTRALIA

[2] ROYAL WOMENS HOSP,DEPT PATHOL,CARLTON,VIC 3053,AUSTRALIA

来源：

ACTA NEUROPATHOLOGICA | 1985年 / 65卷 / 3-4期

关键词：

D O I：

10.1007/BF00687014

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：313 / 317

页数：5

共 10 条

[1] SYNDROME OF SEX-LINKED HYDROCEPHALUS [J].

EDWARDS, JH .

ARCHIVES OF DISEASE IN CHILDHOOD, 1961, 36 (189) :486-&

[2] SEX-LINKED HYDROCEPHALUS - REPORT OF A FAMILY WITH 15 AFFECTED MEMBERS [J].

EDWARDS, JH ;

ROBERTS, JM ;

NORMAN, RM .

ARCHIVES OF DISEASE IN CHILDHOOD, 1961, 36 (189) :481-&

[3] MECHANISM OF ARREST OF NEURONAL MIGRATION IN ZELLWEGER MALFORMATION - HYPOTHESIS BASED UPON CYTOARCHITECTONIC ANALYSIS [J].

EVRARD, P ;

CAVINESS, VS ;

PRATSVINAS, J ;

LYON, G .

ACTA NEUROPATHOLOGICA, 1978, 41 (02) :109-117

[4]

FAIVRE J, 1976, CHILD BRAIN, V2, P226

[5]

FRIEDE RL, 1975, DEV NEUROPATHOLOGY, P342

[6] The rate of spontaneous mutation of a human gene [J].

Haldane, JBS .

JOURNAL OF GENETICS, 1935, 31 (03) :317-326

[7] A FAMILY STUDY OF HYDROCEPHALUS RESULTING FROM AQUEDUCT STENOSIS [J].

HOWARD, FM ;

TILL, K ;

CARTER, CO .

JOURNAL OF MEDICAL GENETICS, 1981, 18 (04) :252-255

[8]

LANDRIEU P, 1979, DEV MED CHILD NEUROL, V21, P637

[9]

PETRUS M, 1981, J GENET HUM, V29, P155

[10] HYDROCEPHALUS, AGYRIA, PSEUDO-ENCEPHALOCELE, RETINAL DYSPLASIA, AND ANTERIOR-CHAMBER ANOMALIES [J].

WINTER, RM ;

GARNER, A .

JOURNAL OF MEDICAL GENETICS, 1981, 18 (04) :314-317

← 1 →