(Q44432410)

2 December 2017

Phenylketonuria mutation in Chinese haplotype 44 identical with haplotype 2 mutation in northern-European Caucasians (English)

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2 December 2017

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T F Tsai

1

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PubMed ID

2323773

2 December 2017

K J Hsiao

series ordinal

2

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PubMed ID

2323773

2 December 2017

T S Su

series ordinal

3

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2 December 2017

1 April 1990

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2 December 2017

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2 December 2017

84

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2 December 2017

5

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2 December 2017

409-411

1 reference

https://scigraph.springernature.com/pub.10.1007/bf00195810

2 December 2017

0 references

cites work

Multiple, independent restriction site polymorphisms in human DNA detected with a cDNA probe to argininosuccinate synthetase (AS)

1 reference

12 December 2020

Phenylalanine hydroxylase gene haplotypes in Polynesians: evolutionary origins and absence of alleles associated with severe phenylketonuria

1 reference

12 December 2020

Phenylpyruvic oligophrenia deficiency of phenylalanine-oxidizing system.

1 reference

12 December 2020

Rapid and efficient site-specific mutagenesis without phenotypic selection

1 reference

12 December 2020

Hybridization of genomic DNA to oligonucleotide probes in the presence of tetramethylammonium chloride

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12 December 2020

DNA sequencing with chain-terminating inhibitors

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12 December 2020

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

1 reference

12 December 2020

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

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12 December 2020

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

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12 December 2020

Screening for phenylketonuria mutations by DNA amplification with the polymerase chain reaction

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12 December 2020

Study of restriction fragment length polymorphisms at the human phenylalanine hydroxylase locus and evaluation of its potential application in prenatal diagnosis of phenylketonuria in Chinese

1 reference

12 December 2020

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

1 reference

12 December 2020

The hydroxylation of phenylalanine and antipyrine in phenylpyruvic oligophrenia.

1 reference

12 December 2020

Identifiers

DOI

10.1007/BF00195810

1 reference

2 December 2017

1 reference

PubMed ID

2323773