(Q46495865)

English

PAH 399 GTA (Val)----GTT(Val), a new silent mutation found in the Chinese

scientific article published in January 1991

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

22 December 2017

http://europepmc.org/abstract/MED/1997387

PAH 399 GTA (Val)----GTT(Val), a new silent mutation found in the Chinese (English)

1 reference

Europe PubMed Central

PubMed publication ID

22 December 2017

http://europepmc.org/abstract/MED/1997387

author name string

S Z Huang

1

1 reference

Europe PubMed Central

PubMed publication ID

22 December 2017

http://europepmc.org/abstract/MED/1997387

Z R Ren

2

1 reference

Europe PubMed Central

PubMed publication ID

22 December 2017

http://europepmc.org/abstract/MED/1997387

Y T Zeng

3

1 reference

Europe PubMed Central

PubMed publication ID

22 December 2017

http://europepmc.org/abstract/MED/1997387

S L Woo

4

1 reference

Europe PubMed Central

PubMed publication ID

22 December 2017

http://europepmc.org/abstract/MED/1997387

publication date

1 January 1991

1 reference

Europe PubMed Central

PubMed publication ID

22 December 2017

http://europepmc.org/abstract/MED/1997387

1 reference

Europe PubMed Central

PubMed publication ID

22 December 2017

http://europepmc.org/abstract/MED/1997387

86

1 reference

Europe PubMed Central

PubMed publication ID

22 December 2017

http://europepmc.org/abstract/MED/1997387

3

1 reference

Europe PubMed Central

PubMed publication ID

22 December 2017

http://europepmc.org/abstract/MED/1997387

305-306

1 reference

Europe PubMed Central

PubMed publication ID

22 December 2017

http://europepmc.org/abstract/MED/1997387

Polymorphic DNA haplotypes at the phenylalanine hydroxylase (PAH) locus in Asian families with phenylketonuria (PKU).

1 reference

https://pubmed.ncbi.nlm.nih.gov/1997387

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A study on Chinese phenylalanine hydroxylase gene restriction site polymorphism

1 reference

https://pubmed.ncbi.nlm.nih.gov/1997387

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/1997387

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

DNA sequencing with chain-terminating inhibitors

1 reference

https://pubmed.ncbi.nlm.nih.gov/1997387

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The enzymatic conversion of phenylalanine to tyrosine.

1 reference

https://pubmed.ncbi.nlm.nih.gov/1997387

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Application of a new DNA sequence polymorphism as a genetic marker in prenatal diagnosis of phenylketonuria

1 reference

https://pubmed.ncbi.nlm.nih.gov/1997387

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/1997387

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/1997387

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Primer-directed enzymatic amplification of DNA with a thermostable DNA polymerase

1 reference

https://pubmed.ncbi.nlm.nih.gov/1997387

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Collation of RFLP haplotypes at the human phenylalanine hydroxylase (PAH) locus

1 reference

https://pubmed.ncbi.nlm.nih.gov/1997387

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

An improved method for prenatal diagnosis of genetic diseases by analysis of amplified DNA sequences. Application to hemophilia A.

1 reference

https://pubmed.ncbi.nlm.nih.gov/1997387

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Molecular structure and polymorphic map of the human phenylalanine hydroxylase gene

1 reference

https://pubmed.ncbi.nlm.nih.gov/1997387

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/1997387

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Construction of human gene libraries from small amounts of peripheral blood: analysis of beta-like globin genes

1 reference

https://pubmed.ncbi.nlm.nih.gov/1997387

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Molecular genetics of phenylketonuria in Orientals: linkage disequilibrium between a termination mutation and haplotype 4 of the phenylalanine hydroxylase gene.

1 reference

https://pubmed.ncbi.nlm.nih.gov/1997387

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Recurrent mutation, gene conversion, or recombination at the human phenylalanine hydroxylase locus: evidence in French-Canadians and a catalog of mutations

1 reference

https://pubmed.ncbi.nlm.nih.gov/1997387

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/BF00202416

1 reference

Europe PubMed Central

PubMed publication ID

22 December 2017

http://europepmc.org/abstract/MED/1997387

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

22 December 2017

http://europepmc.org/abstract/MED/1997387

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