(Q53042601)

English

Linkage disequilibrium between RFLP haplotype 2 and the affected PAH allele in PKU families from the Berlin area of the German Democratic Republic.

scientific article published in April 1988

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

10 May 2018

http://europepmc.org/abstract/MED/2896155

Linkage disequilibrium between RFLP haplotype 2 and the affected PAH allele in PKU families from the Berlin area of the German Democratic Republic. (English)

1 reference

Europe PubMed Central

PubMed publication ID

10 May 2018

http://europepmc.org/abstract/MED/2896155

1 reference

based on heuristic

inferred from title

linkage disequilibrium

1 reference

based on heuristic

inferred from title

author name string

O Riess

1

1 reference

Europe PubMed Central

PubMed publication ID

10 May 2018

http://europepmc.org/abstract/MED/2896155

A Michel

2

1 reference

Europe PubMed Central

PubMed publication ID

10 May 2018

http://europepmc.org/abstract/MED/2896155

A Speer

3

1 reference

Europe PubMed Central

PubMed publication ID

10 May 2018

http://europepmc.org/abstract/MED/2896155

W Meiske

4

1 reference

Europe PubMed Central

PubMed publication ID

10 May 2018

http://europepmc.org/abstract/MED/2896155

G Cobet

5

1 reference

Europe PubMed Central

PubMed publication ID

10 May 2018

http://europepmc.org/abstract/MED/2896155

C Coutelle

6

1 reference

Europe PubMed Central

PubMed publication ID

10 May 2018

http://europepmc.org/abstract/MED/2896155

publication date

1 April 1988

1 reference

Europe PubMed Central

PubMed publication ID

10 May 2018

http://europepmc.org/abstract/MED/2896155

1 reference

Europe PubMed Central

PubMed publication ID

10 May 2018

http://europepmc.org/abstract/MED/2896155

78

1 reference

Europe PubMed Central

PubMed publication ID

10 May 2018

http://europepmc.org/abstract/MED/2896155

4

1 reference

Europe PubMed Central

PubMed publication ID

10 May 2018

http://europepmc.org/abstract/MED/2896155

343-346

1 reference

Europe PubMed Central

PubMed publication ID

10 May 2018

http://europepmc.org/abstract/MED/2896155

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/2896155

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Recurrent mutations in haemophilia A give evidence for CpG mutation hotspots

1 reference

https://pubmed.ncbi.nlm.nih.gov/2896155

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/2896155

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/2896155

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Molecular analysis of the inheritance of phenylketonuria and mild hyperphenylalaninemia in families with both disorders

1 reference

https://pubmed.ncbi.nlm.nih.gov/2896155

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Molecular genetics of PKU

1 reference

https://pubmed.ncbi.nlm.nih.gov/2896155

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Typing of families with classical phenylketonuria using three alleles of the Hindiii linked restriction fragment polymorphism, detectable with a phenylalanine hydroxylase cDNA probe. Family typing for PKU by linked HindIII RFLP.

1 reference

https://pubmed.ncbi.nlm.nih.gov/2896155

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/2896155

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/BF00291732

1 reference

Europe PubMed Central

PubMed publication ID

10 May 2018

http://europepmc.org/abstract/MED/2896155

release_5lwgbx6525gzzaizqj6ka6mlyu

1 reference

https://api.fatcat.wiki/v0/release/5lwgbx6525gzzaizqj6ka6mlyu

24 November 2022

based on heuristic

mapped directly with Wikidata item

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

10 May 2018

http://europepmc.org/abstract/MED/2896155

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