(Q35200406)

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Extensive restriction site polymorphism at the human phenylalanine hydroxylase locus and application in prenatal diagnosis of phenylketonuria

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11 November 2019

Extensive restriction site polymorphism at the human phenylalanine hydroxylase locus and application in prenatal diagnosis of phenylketonuria (English)

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9556654%20AND%20SRC:MED&resulttype=core&format=json

11 November 2019

phenylketonuria

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Stephen P. Daiger

5

object named as

S P Daiger

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7 August 2017

author name string

A S Lidsky

1

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11 November 2019

F D Ledley

2

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11 November 2019

A G DiLella

3

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11 November 2019

S C Kwok

4

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11 November 2019

K J Robson

6

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11 November 2019

S L Woo

7

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11 November 2019

S P Daiger

5

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11 November 2019

language of work or name

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publication date

1 July 1985

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11 November 2019

American Journal of Human Genetics

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11 November 2019

37

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11 November 2019

619-634

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11 November 2019

4

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11 November 2019

Studies on phenylketonuria. I. Restricted phenylalanine intake in phenylketonuria

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684630

13 July 2018

A SIMPLE PHENYLALANINE METHOD FOR DETECTING PHENYLKETONURIA IN LARGE POPULATIONS OF NEWBORN INFANTS

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684630

13 July 2018

Polysome immunoprecipitation of phenylalanine hydroxylase mRNA from rat liver and cloning of its cDNA.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684630

13 July 2018

The PKU locus in man is on chromosome 12.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684630

13 July 2018

A polymorphic DNA marker genetically linked to Huntington's disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684630

13 July 2018

Molecular genetics of human serum albumin: restriction enzyme fragment length polymorphisms and analbuminemia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684630

13 July 2018

Linkage of beta-thalassaemia mutations and beta-globin gene polymorphisms with DNA polymorphisms in human beta-globin gene cluster.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684630

13 July 2018

Construction of a genetic linkage map in man using restriction fragment length polymorphisms

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684630

13 July 2018

Nucleotide sequence of a full-length complementary DNA clone and amino acid sequence of human phenylalanine hydroxylase

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684630

13 July 2018

Detection of specific sequences among DNA fragments separated by gel electrophoresis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684630

13 July 2018

Nucleotide sequence of the rightward operator of phage lambda

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684630

13 July 2018

Effect of stopping low-phenylalanine diet on intellectual progress of children with phenylketonuria

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684630

13 July 2018

DNA sequence variants in the G gamma-, A gamma-, delta- and beta-globin genes of man

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684630

13 July 2018

The influence of phenylalanine intake on the chemistry and behaviour of a phenyl-ketonuric child.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684630

26 September 2018

Phenylpyruvic oligophrenia deficiency of phenylalanine-oxidizing system.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684630

26 September 2018

Cloned human phenylalanine hydroxylase gene allows prenatal diagnosis and carrier detection of classical phenylketonuria

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684630

26 September 2018

Quantification of the close association between DNA haplotypes and specific β-thalassaemia mutations in Mediterraneans

1 reference

https://pubmed.ncbi.nlm.nih.gov/9556654

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Frequency of inborn errors of metabolism, especially PKU, in some representative newborn screening centers around the world: a collaborative study

1 reference

https://pubmed.ncbi.nlm.nih.gov/9556654

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Restriction sites containing CpG show a higher frequency of polymorphism in human DNA

1 reference

https://pubmed.ncbi.nlm.nih.gov/9556654

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Linkage relationship of a cloned DNA sequence on the short arm of the X chromosome to Duchenne muscular dystrophy

1 reference

https://pubmed.ncbi.nlm.nih.gov/9556654

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Prenatal diagnosis of classic phenylketonuria by DNA analysis

1 reference

https://pubmed.ncbi.nlm.nih.gov/9556654

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Diet discontinuation policies and practices of PKU clinics in the United States

1 reference

https://pubmed.ncbi.nlm.nih.gov/9556654

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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11 November 2019

1 reference

Europe PubMed Central

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11 November 2019

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