PRENATAL DIAGNOSIS OF INBORN ERRORS OF METABOLISM

被引:34
作者
MILUNSKY, A
LITTLEFIELD, JW
机构
来源
ANNUAL REVIEW OF MEDICINE | 1972年 / 23卷 / 05期
关键词
D O I
10.1146/annurev.me.23.020172.000421
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
引用
收藏
页码:57 / +
页数:1
相关论文
共 189 条
[61]  
HOLTZ AI, 1964, FED PROC, V23, P128
[62]  
HORSCAYLA MC, 1968, ANN GENET-PARIS, V11, P265
[63]   TYPE-IV GLYCOGEN STORAGE DISEASE - BRANCHING ENZYME DEFICIENCY IN SKIN FIBROBLASTS AND POSSIBLE HETEROZYGOTE DETECTION [J].
HOWELL, RR ;
KABACK, MM ;
BROWN, BI .
JOURNAL OF PEDIATRICS, 1971, 78 (04) :638-+
[64]  
HOWELL RR, 1967, B JOHNS HOPKINS HOSP, V120, P81
[65]  
HSIA YE, 1969, LANCET, V1, P757
[66]   INHERITED PROPIONYL-COA CARBOXYLASE DEFICIENCY IN KETOTIC-HYPERGLYCINEMIA [J].
HSIA, YE ;
SCULLY, KJ ;
ROSENBERG, LE .
JOURNAL OF CLINICAL INVESTIGATION, 1971, 50 (01) :127-+
[67]  
HUG G, 1971, AM PEDIAT SOC SOC PE, P118
[68]  
HUIJING F, 1968, ACTA GENET STAT MED, V18, P128
[69]   HUMAN CYSTINOSIS - INTRACELLULAR DEPOSITION OF CYSTINE [J].
HUMMELER, K ;
ZAJAC, BA ;
GENEL, M ;
HOLTZAPPLE, PG ;
SEGAL, S .
SCIENCE, 1970, 168 (3933) :859-+
[70]  
JACOBY LB, TO BE PUBLISHED