SYNDROME OF CAMPTODACTYLY, MULTIPLE ANKYLOSES, FACIAL ANOMALIES, AND PULMONARY HYPOPLASIA - LETHAL CONDITION

被引：157

作者：

PENA, SDJ

SHOKEIR, MHK

机构：

[1] UNIV MANITOBA, HLTH SCI CHILDRENS CTR, DIV GENET, WINNIPEG R3E OW1, MANITOBA, CANADA

[2] UNIV MANITOBA, DEPT PEDIAT, WINNIPEG R3E OW1, MANITOBA, CANADA

来源：

关键词：

D O I：

10.1016/S0022-3476(74)80119-8

中图分类号：

R72 [儿科学];

学科分类号：

100202 ;

摘要：

引用

页码：373 / 375

页数：3

共 5 条

[1] CURRARINO G, 1964, J ROENTGENOL, V92, P1312
[2] DENNYBROWN DE, 1957, J NEUROPATHOL EXP NE, V16, P119
[3] CAMPTODACTYLY - OCCURRENCE IN 2 NEW GENETIC SYNDROMES AND ITS RELATIONSHIP TO OTHER SYNDROMES
GOODMAN, RM
BATMIRIA.M
MANOR, E
[J]. JOURNAL OF MEDICAL GENETICS, 1972, 9 (02) : 203 - &
[4] HIGGINS JV, 1972, AM J HUM GENET, V24, pA58
[5] ARTHROGRYPOSIS MULTIPLEX CONGENITA
MEAD, NG
LITHGOW, WC
SWEENEY, HJ
[J]. JOURNAL OF BONE AND JOINT SURGERY-AMERICAN VOLUME, 1958, 40 (06) : 1285 - 1309