Screening Newborns for Hereditary Metabolic Disease-Reference-Cited by-同舟云学术

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Screening Newborns for Hereditary Metabolic Disease

Published:1965-08 Issue:3 Volume:12 Page:807-821
ISSN:0031-3955
Container-title:Pediatric Clinics of North America
language:en
Short-container-title:Pediatric Clinics of North America

Author:

Scriver Charles R.

Publisher

Elsevier BV

Subject

Pediatrics, Perinatology and Child Health

Reference34 articles.

1. Biochemistry;Armstrong,1963

2. Procedures for Testing Urine Specimens Dried on Filter Paper;Berry;Clin. Chem.,1959

3. Procedures for Testing Urine Dried on Filter Paper: A Microbiological Test for Leucine, Valine and Isoleucine;Berry;Clin. Chem.,1962

4. Detection of Metabolic Disorders among Mentally Retarded Children by Means of Paper Spot Tests;Berry;Am. J. Ment. Deficiency,1962

5. New Methods for Detection of Galactosemia and Its Carrier State;Beutler;J. Lab. & Clin. Med.,1964

Cited by 10 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. Neonatal Mass Screening of Hereditary Metabolic Diseases in S. Paulo-Brasil;Pediatrics International;1980-03

2. Screening for metabolic disorders in children-aminoacidopathies;The Indian Journal of Pediatrics;1977-02

3. Genetic screening and allied services: structure, process and objective;Medico-Social Management of Inherited Metabolic Disease;1977

4. Screening in Pediatric Practice;Pediatric Clinics of North America;1974-02

5. On the screening, diagnosis and investigation of hereditary aminoacidopathies;Clinical Biochemistry;1973-03

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