GENETICS AND DISEASES OF MUSCLE

被引:19
作者
BOYER, SH
FAINER, DC
机构
关键词
D O I
10.1016/0002-9343(63)90134-7
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
引用
收藏
页码:622 / +
页数:1
相关论文
共 89 条
[61]   COLOUR BLINDNESS AND THE DUCHENNE-TYPE MUSCULAR DYSTROPHY [J].
PHILIP, U ;
WALTON, JN .
ANNALS OF HUMAN GENETICS, 1956, 21 (02) :155-156
[62]   A THIRD TYPE OF PERIODIC PARALYSIS, WITH NORMOKALEMIA AND FAVOURABLE RESPONSE TO SODIUM CHLORIDE [J].
POSKANZER, D ;
KERR, DNS .
AMERICAN JOURNAL OF MEDICINE, 1961, 31 (03) :328-&
[64]   NAIL-PATELLA SYNDROME - EVIDENCE FOR MODIFICATION BY ALLELES AT THE MAIN LOCUS [J].
RENWICK, JH .
ANNALS OF HUMAN GENETICS, 1956, 21 (02) :159-169
[65]  
RICHTERICH R, 1963, AM J HUM GENET, V15, P133
[66]  
ROBBINS PW, 1960, FED PROC, V19, P193
[67]  
ROSSIFANELLI A, 1959, CIBA F S BIOCHEM HUM, P144
[68]  
ROWLEY P, 1960, RES PUBL A NERV MENT, V38, P274
[69]   CHRONIC PROGRESSIVE MYOPATHY WITH MYOGLOBINURIA - DEMONSTRATION OF A GLYCOGENOLYTIC DEFECT IN THE MUSCLE [J].
SCHMID, R ;
MAHLER, R .
JOURNAL OF CLINICAL INVESTIGATION, 1959, 38 (11) :2044-2058
[70]   HEREDITARY ABSENCE OF MUSCLE PHOSPHORYLASE (MCARDLES SYNDROME) [J].
SCHMID, R ;
HAMMAKER, L .
NEW ENGLAND JOURNAL OF MEDICINE, 1961, 264 (05) :223-+