DYGGVE-MELCHIOR-CLAUSEN SYNDROME

被引：41

作者：

SPRANGER, J

MAROTEAUX, P

DERKALOUSTIAN, VM

机构：

[1] UNIV KIEL,DEPT PEDIAT,KIEL,FED REP GER

[2] HOP ENFANTS MALAD,DEPT MED GENET,PARIS,FRANCE

[3] AMER UNIV,SCH MED,DEPT PEDIAT,BEIRUT,LEBANON

来源：

RADIOLOGY | 1975年 / 114卷 / 02期

关键词：

D O I：

10.1148/114.2.415

中图分类号：

R8 [特种医学]; R445 [影像诊断学];

学科分类号：

1002 ; 100207 ; 1009 ;

摘要：

引用

页码：415 / 421

页数：7

共 18 条

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[2] CHEMICAL AND ENZYMIC STUDIES OF A FAMILY WITH SKELETAL ABNORMALITIES ASSOCIATED WITH MENTAL RETARDATION [J].

CLAUSEN, J ;

DYGGVE, HV ;

MELCHIOR, JC .

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[3] MUCOPOLYSACCHARIDOSIS - PAPER ELECTROPHORETIC AND INFRA-RED ANALYSIS OF URINE IN GARGOYLISM AND MORQUIO-ULLRICHS DISEASE [J].

CLAUSEN, J ;

DYGGVE, HV ;

MELCHIOR, JC .

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[4] MORQUIO-ULLRICHS DISEASE - AN INBORN ERROR OF METABOLISM [J].

DYGGVE, HV ;

MELCHIOR, JC ;

CLAUSEN, J .

ARCHIVES OF DISEASE IN CHILDHOOD, 1962, 37 (195) :525-&

[5]

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[6]

Giedion A, 1968, ERGB MED RADIOL, V1, P59

[7] RADIOLOGICAL CASE OF MONTH - MORQUIO-BRAILSFORD DISEASE [J].

GWINN, JL ;

BARNES, GR .

AMERICAN JOURNAL OF DISEASES OF CHILDREN, 1968, 115 (03) :347-&

[8]

HOBAEK A, 1961, PROBLEMS HEREDITARY, P64

[9]

KAUFMAN R L, 1971, Birth Defects Original Article Series, V7, P144

[10]

LANGER LO, 1966, AMER J ROENTGENOL RA, V97, P1

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