GENETIC IMPLICATIONS FOR NEWBORN SCREENING FOR PHENYLKETONURIA-Reference-Cited by-同舟云学术

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GENETIC IMPLICATIONS FOR NEWBORN SCREENING FOR PHENYLKETONURIA

Published:2001-06 Issue:2 Volume:28 Page:419-424
ISSN:0095-5108
Container-title:Clinics in Perinatology
language:en
Short-container-title:Clinics in Perinatology

Author:

Cruz Felix de la,Koch Richard

Publisher

Elsevier BV

Subject

Obstetrics and Gynecology,Pediatrics, Perinatology and Child Health

Reference25 articles.

1. Maternal phenylketonuria and fetal brain damage: An attempt at prevention by dietary control;Allan,1968

2. Newborn screening fact sheet;American Academy of Pediatrics Committee on Genetics;Pediatrics,1996

3. Intellectual development in 12 year old children treated for phenylketonuria;Azen;Am J Dis Child,1991

4. Influence of phenylalanine intake on phenylketonuria;Bickel;Lancet,1953

5. Expansion of newborn screening programs using automated tandem mass spectrometry;Chace;Ment Retard,1999

Cited by 5 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. From The Cover: Correction of kinetic and stability defects by tetrahydrobiopterin in phenylketonuria patients with certain phenylalanine hydroxylase mutations;Proceedings of the National Academy of Sciences;2004-11-19

2. Future directions;Best Practice & Research Clinical Obstetrics & Gynaecology;2002-10

3. Future Directions;Clinical Obstetrics and Gynecology;2002-09

4. FUTURE DIRECTIONS;Clinics in Perinatology;2001-06

5. Current Awareness;Prenatal Diagnosis;2001

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