DYGGVE-MELCHIOR-CLAUSEN SYNDROME

被引:29
作者
BEIGHTON, P
机构
[1] MRC Res. U. Inherited Skeletal D., Department of Human Genetics, Univ. of Cape Town Medical School, Cape Town
关键词
D O I
10.1136/jmg.27.8.512
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
[No abstract available]
引用
收藏
页码:512 / 515
页数:4
相关论文
共 17 条
[1]   DYGGVE-MELCHIOR-CLAUSEN SYNDROME - NORMAL DEGRADATION OF PROTEODERMATAN SULFATE, PROTEOKERATAN SULFATE AND HEPARAN-SULFATE [J].
BECK, M ;
LUCKE, R ;
KRESSE, H .
CLINICA CHIMICA ACTA, 1984, 141 (01) :7-15
[2]  
Beemer F A, 1984, Tijdschr Kindergeneeskd, V52, P103
[3]  
BONAFEDE RP, 1978, CLIN GENET, V14, P24
[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]   CASE REPORT-431 - DYGGVE-MELCHIOR-CLAUSEN SYNDROME (DMCS) [J].
HALLCRAGGS, MA ;
CHAPMAN, M .
SKELETAL RADIOLOGY, 1987, 16 (05) :422-424
[6]  
HOBAEK A, 1961, PROBLEMS HEREDITARY
[7]  
MCKUSICK VA, 1989, MENDELIAN INHERITANC
[8]  
NAFFAH J, 1976, AM J HUM GENET, V28, P607
[9]  
NAFFAH J, 1974, ARCH FR PEDIATR, V31, P985
[10]  
RASTOGI SC, 1977, ACTA NEUROL SCAND, V56, P389