Molecular diagnosis and inborn errors of metabolism: A practitioner’s view-Reference-Cited by-同舟云学术

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Molecular diagnosis and inborn errors of metabolism: A practitioner’s view

Published:2000-11 Issue:6 Volume:2 Page:345-349
ISSN:1098-3600
Container-title:Genetics in Medicine
language:en
Short-container-title:Genetics in Medicine

Author:

Cederbaum Stephen

Publisher

Elsevier BV

Subject

Genetics (clinical)

Reference15 articles.

1. Polysome immuno-precip- itation of phenylalanine hydroxylase mRNA from rat liver and cloning of its cDNA;Robson;Proc Natl Acad Sa USA,1982

2. Molecular cloning of the cDNA coding for rat ornithine transcarbamylase;Horwich;Proc Natl Acad Sci USA,1983

3. Molecular basis of hyperargininemia: structure-function consequences of mutations in human liver arginase;Ash;Mol Genet Metab,1998

4. α-Antitrypsin deficiency;Cox,1995

5. Outcome of individuals with low-moderate methylmalonic aciduria detected through a neonatal screening programs;Sniderman;J Pediatr,1999

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1. Resetting our Educational Sights: Unconstructing the Public's Dreams and Nightmares of the Genetic Revolution*;The American Journal of Human Genetics;2001-04

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