Literature DB >> 14162582

TESTING OF NEWBORN SIBLINGS IN PHENYLKETONURIC FAMILIES.

H K BERRY, B UMBARGER, B SUTHERLAND.   

Abstract

Keywords:  BLOOD CHEMICAL ANALYSIS; GENETICS, HUMAN; INFANT, NEWBORN; PHENYLACETATES; PHENYLALANINE; PHENYLKETONURIA; URINE

Mesh：

Substances：

Year:  1964        PMID： 14162582     DOI： 10.1001/jama.1964.03070080047018

Source DB:  PubMed          Journal:  JAMA        ISSN： 0098-7484            Impact factor:   56.272


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  4 in total

1.  Population screening by Guthrie test for phenylketonuria in South-east Scotland. Report by the consultant paediatricians and medical officers of health of the S.E. Scotland Hospital Region.

Authors: 
Journal:  Br Med J       Date:  1968-03-16

2.  Phenylketonuria. Early detection, diagnosis and treatment.

Authors:  G C Cunningham
Journal:  Calif Med       Date:  1966-07

3.  Present status of different mass screening procedures for phenylketonuria. Medical Research Council Working Party on phenylketonuria.

Authors: 
Journal:  Br Med J       Date:  1968-10-05

4.  Fifteen-year experience with screening for phenylketonuria with an automated fluorometric method.

Authors:  H N Kirkman; C L Carroll; E G Moore; M S Matheson
Journal:  Am J Hum Genet       Date:  1982-09       Impact factor: 11.025
  4 in total

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