SCREENING TESTS FOR BIOCHEMICAL DEFECTS IN INFANCY

Author:

Pitt David1

Affiliation:

1. Melbourne

Publisher

AMPCo

Subject

General Medicine

Reference7 articles.

1. Procedures for Testing Urine Specimens Dried on Filter Paper

2. Preliminary Communication

3. Some Problems in the Diagnosis of Phenylketonuria;Danks D.;Med. J. Aust.,1964

4. Guthrie R. andWhitne S.(1964) “Phenylketonuria. Detection in the Newborn Infant as a Routine Hospital Procedure” Children's Bureau Publication No. 419 Washington U.S.A.

Cited by 3 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

1. Phenylketonuria Testing - Its Role in Pediatrics and Public Health;CRC Critical Reviews in Clinical Laboratory Sciences;1971-01

2. Rapid Technique for the Presymptomatic Detection of Inborn Errors of Amino Acid Metabolism;Annals of Clinical Biochemistry: International Journal of Laboratory Medicine;1969-03

3. DETECTION OF URINARY ABNORMALITIES IN A WELL‐BABY POPULATION: RESULTS OF A SURVEY;Medical Journal of Australia;1967-03

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