Typing of families with classical phenylketonuria using three alleles of the Hindlll linked restriction fragment polymorphism, detectable with a phenylalanine hydroxylase cDNA probe-Reference-Cited by-同舟云学术

Typing of families with classical phenylketonuria using three alleles of the Hindlll linked restriction fragment polymorphism, detectable with a phenylalanine hydroxylase cDNA probe

Published:2008-04-23 Issue:6 Volume:29 Page:491-495
ISSN:0009-9163
Container-title:Clinical Genetics
language:en
Short-container-title:

Author:

Speer A.,Dahl H.-H.,Riess O.,Cobet G.,Hanke R.,Cotton R. G. H.,Coutelle Ch.

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.1986.tb00549.x/fullpdf

Reference9 articles.

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3. A simple phenylalanine method for the detection of phenylketonuria in a large population of newborn infants.;Guthrie;Pediatrics,1963

4. Nucleotide sequence of a full-length complementary DNA clone and aminoacid sequence of human phenylalanine hydroxylase.;Kwok;Biochemistry,1985

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1. Haplotype analysis of the phenylalanine hydroxylase gene in Turkish phenylketonuria families;Clinical Genetics;2008-06-28

2. Introduction of genomic diagnosis of classical phenylketonuria to the health care system of the German Democratic Republic;Clinical Genetics;2008-06-28

3. 6 Molecular Genetics of Phenylketonuria: From Molecular Anthropology to Gene Therapy;Advances in Genetics;1995

4. Heterogeneity of phenylketonuria at the clinical, protein and DNA levels;Journal of Inherited Metabolic Disease;1990-09

5. Genomics in the German Democratic Republic;Genomics;1990-09