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Linkage disequilibrium between mutation and RFLP haplotype at the phenylalanine hydroxylase locus in the German population (Q69916655)

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scientific article published on 01 April 1988

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English	Linkage disequilibrium between mutation and RFLP haplotype at the phenylalanine hydroxylase locus in the German population	scientific article published on 01 April 1988

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scholarly article

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2896156%20AND%20SRC:MED&resulttype=core&format=json

6 October 2019

Linkage disequilibrium between mutation and RFLP haplotype at the phenylalanine hydroxylase locus in the German population (English)

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2896156%20AND%20SRC:MED&resulttype=core&format=json

6 October 2019

1 reference

based on heuristic

inferred from title

linkage disequilibrium

1 reference

based on heuristic

inferred from title

author name string

U Lichter-Konecki

1

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2896156%20AND%20SRC:MED&resulttype=core&format=json

6 October 2019

M Schlotter

2

1 reference

Europe PubMed Central

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6 October 2019

D S Konecki

3

1 reference

Europe PubMed Central

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6 October 2019

S Labeit

4

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2896156%20AND%20SRC:MED&resulttype=core&format=json

6 October 2019

S L Woo

5

1 reference

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6 October 2019

F K Trefz

6

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6 October 2019

publication date

1 April 1988

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6 October 2019

language of work or name

0 references

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2896156%20AND%20SRC:MED&resulttype=core&format=json

6 October 2019

78

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Europe PubMed Central

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6 October 2019

4

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6 October 2019

347-352

1 reference

Europe PubMed Central

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6 October 2019

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/2896156

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/2896156

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Base composition-independent hybridization in tetramethylammonium chloride: a method for oligonucleotide screening of highly complex gene libraries

1 reference

https://pubmed.ncbi.nlm.nih.gov/2896156

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Polymorphic DNA haplotypes at the human phenylalanine hydroxylase locus and their relationship with phenylketonuria

1 reference

https://pubmed.ncbi.nlm.nih.gov/2896156

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Polymer support oligonucleotide synthesis XVIII: use of beta-cyanoethyl-N,N-dialkylamino-/N-morpholino phosphoramidite of deoxynucleosides for the synthesis of DNA fragments simplifying deprotection and isolation of the final product

1 reference

https://pubmed.ncbi.nlm.nih.gov/2896156

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Correlation between polymorphic DNA haplotypes at phenylalanine hydroxylase locus and clinical phenotypes of phenylketonuria

1 reference

https://pubmed.ncbi.nlm.nih.gov/2896156

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Sensitive in vivo assay of the phenylalanine hydroxylating system with a small intravenous dose of heptadeutero l-phenylalanine using high pressure liquid chromatography and capillary gas chromatography/mass fragmentography

1 reference

https://pubmed.ncbi.nlm.nih.gov/2896156

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/2896156

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Phenylalaninaemia. Differential diagnosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/2896156

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Enzymatic amplification of beta-globin genomic sequences and restriction site analysis for diagnosis of sickle cell anemia

1 reference

https://pubmed.ncbi.nlm.nih.gov/2896156

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Patterns of polymorphism and linkage disequilibrium suggest independent origins of the human growth hormone gene cluster

1 reference

https://pubmed.ncbi.nlm.nih.gov/2896156

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/2896156

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Tight linkage between a splicing mutation and a specific DNA haplotype in phenylketonuria

1 reference

https://pubmed.ncbi.nlm.nih.gov/2896156

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Polymorphic DNA haplotypes at the phenylalanine hydroxylase locus in prenatal diagnosis of phenylketonuria

1 reference

https://pubmed.ncbi.nlm.nih.gov/2896156

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/2896156

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Determination of Phenylalanine Hydroxylase Activity in Patients with Phenylketonuria and Hyperphenylalaninemia

1 reference

https://pubmed.ncbi.nlm.nih.gov/2896156

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Phenylalanine hydroxylase deficiency caused by a single base substitution in an exon of the human phenylalanine hydroxylase gene

1 reference

https://pubmed.ncbi.nlm.nih.gov/2896156

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

An amino-acid substitution involved in phenylketonuria is in linkage disequilibrium with DNA haplotype 2.

1 reference

https://pubmed.ncbi.nlm.nih.gov/2896156

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Phenylketonuria. Population genetics of a disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/2896156

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Analysis of enzymatically amplified β-globin and HLA-DQα DNA with allele-specific oligonucleotide probes

1 reference

https://pubmed.ncbi.nlm.nih.gov/2896156

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Allele-specific hybridization using oligonucleotide probes of very high specific activity: discrimination of the human beta A- and beta S-globin genes

1 reference

https://pubmed.ncbi.nlm.nih.gov/2896156

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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