MONOGENIC DISORDERS

被引:77
作者
CARTER, CO [1 ]
机构
[1] INST CHILD HLTH,MRC,CLIN GENET UNIT INST CHILD HLTH,LONDON WC1N 1EH,ENGLAND
关键词
D O I
10.1136/jmg.14.5.316
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
引用
收藏
页码:316 / 320
页数:5
相关论文
共 42 条
[1]  
Beighton P, 1970, EHLERS DANLOS SYNDRO
[2]   POLYCYSTIC DISEASE OF KIDNEYS AND LIVER PRESENTING IN CHILDHOOD [J].
BLYTH, H ;
OCKENDEN, BG .
JOURNAL OF MEDICAL GENETICS, 1971, 8 (03) :257-+
[3]  
BORBERG A, 1951, ACTA PSYCHIATRIC S71
[4]   FAMILIAL HYPERCHOLESTEROLEMIA - DEFECTIVE BINDING OF LIPOPROTEINS TO CULTURED FIBROBLASTS ASSOCIATED WITH IMPAIRED REGULATION OF 3-HYDROXY-3-METHYLGLUTARYL COENZYME A REDUCTASE-ACTIVITY [J].
BROWN, MS ;
GOLDSTEIN, JL .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1974, 71 (03) :788-792
[5]  
CARTER CO, 1973, J BIOSOC SCI, V5, P261
[6]  
CERVENKA J, 1967, AM J HUM GENET, V19, P416
[7]  
CHUNG CS, 1958, ANN HUM GENET, V23, P357
[8]  
CROWE FW, 1956, CLINICAL PATHOLOGICA
[9]  
DALGAARD OZ, 1957, ACTA MEDICA SCA S328
[10]  
FRASER GR, 1967, CAUSES BLINDNESS CHI