SPONDYLOMETEPIPHYSEAL DYSPLASIA, STRUDWICK TYPE

被引：44

作者：

ANDERSON, CE

SILLENCE, DO

LACHMAN, RS

TOOMEY, K

BULL, M

DORST, J

RIMOIN, DL

机构：

[1] UNIV SYDNEY,DEPT SOCIAL & PREVENT MED,SYDNEY,NSW 2006,AUSTRALIA

[2] UNIV CALIF LOS ANGELES,DEPT RADIOL & PEDIAT,LOS ANGELES,CA 90024

[3] UNIV CALIF LOS ANGELES,DEPT PEDIAT & MED,LOS ANGELES,CA 90024

[4] UNIV CALIF LOS ANGELES,LOS ANGELES CTY HARBOR MED CTR,DEPT PEDIAT,TORRANCE,CA 90509

[5] GEORGE WASHINGTON UNIV,CHILDRENS HOSP,NATL MED CTR,DEPT PEDIAT,WASHINGTON,DC 20010

[6] INDIANA UNIV,DEPT PEDIAT,INDIANAPOLIS,IN 46204

[7] JOHNS HOPKINS UNIV,DEPT RADIOL,BALTIMORE,MD 21218

来源：

AMERICAN JOURNAL OF MEDICAL GENETICS | 1982年 / 13卷 / 03期

关键词：

D O I：

10.1002/ajmg.1320130304

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

引用

页码：243 / 256

页数：14

共 11 条

[1]

DIAMOND L, 1974, SKELETAL DYSPLASIAS, P412

[2] COMBINED METAPHYSEAL AND EPIPHYSEAL DYSOSTOSIS - REPORT OF 2 CASES - ONE IN WHICH METAPHYSEAL CHANGES PREDOMINATE AND A SECOND ONE IN WHICH EPIPHYSEAL CHANGES ARE MORE MARKED [J].

KOZLOWSK.K ;

BUDZINSK.A .

AMERICAN JOURNAL OF ROENTGENOLOGY RADIUM THERAPY AND NUCLEAR MEDICINE, 1966, 97 (01) :21-&

[3]

LACHMAN RS, 1977, DISORDERS CONNECTIVE

[4]

Lee M M, 1968, Invest Radiol, V3, P96, DOI 10.1097/00004424-196803000-00007

[5]

MCKUSICK VA, 1978, MENDELIAN INHERITANC, P357

[6]

MURDOCH LG, 1969, SKELETAL DYSPLASIA 4, P368

[7]

RIMOIN DL, 1975, ADV HUMAN GENETICS, P10

[8]

SILLENCE DO, 1979, AM J PATHOL, V96, P812

[9]

SUTCLIFFE J, 1966, ANN RADIOL, V9, P215

[10]

WILLIAMS BR, 1974, SKELETAL DYSPLASIAS, P75

← 1 2 →