PHENYLKETONURIA - MASS SCREENING OF NEWBORNS IN IRELAND

被引:40
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CAHALANE, SF
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10.1136/adc.43.228.141
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R72 [儿科学];
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100202 ;
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页码:141 / &
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[1]   ATYPICAL PHENYLKETONURIC HETEROZYGOTE [J].
ANDERSON, JA ;
FISCH, R ;
MILLER, E ;
DOEDEN, D .
JOURNAL OF PEDIATRICS, 1966, 68 (03) :351-+
[2]  
AUERBACH VH, 1966, P SOC PEDIAT RES, V108
[3]  
BAKER JR, 1964, J MENT DEFIC RES, V8, P176
[4]  
CAHALANE S F, 1964, J Ir Med Assoc, V54, P88
[5]   BIRTHPLACES OF PARENTS AND GRANDPARENTS OF A SRIES OF PATIENTS WITH PHENYLKETONURIA IN SOUTH-EAST ENGLAND [J].
CARTER, CO ;
WOOLF, LI .
ANNALS OF HUMAN GENETICS, 1961, 25 (01) :57-&
[6]  
CENTERWALL WR, 1963, PHENYLKETONURIA, P115
[7]  
COHEN BE, 1966, ISRAEL J MED SCI, V2, P156
[8]   SIMPLE CHROMATOGRAPHIC SCREENING TEST FOR DETECTION OF DISORDERS OF AMINO ACID METABOLISM [J].
EFRON, ML ;
MACCREADY, RA ;
YOUNG, D ;
MOSER, HW .
NEW ENGLAND JOURNAL OF MEDICINE, 1964, 270 (26) :1378-+
[9]  
GUTHRIE R, 1963, PEDIATRICS, V32, P338
[10]  
GUTHRIE R, 1964, PHENYLKETONURIA DETE, P33