(Q57218515)

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10 September 2022

Y. Hase

2

1 reference

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10 September 2022

D. H. Lee

3

1 reference

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10 September 2022

J. Furuyama

4

1 reference

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10 September 2022

H. Shintaku

5

1 reference

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10 September 2022

T. Oura

6

1 reference

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10 September 2022

G. Isshiki

7

1 reference

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A single origin of phenylketonuria in Yemenite Jews

10 September 2022

language of work or name

English

0 references

publication date

1992

0 references

published in

Human Mutation

0 references

volume

1

0 references

issue

3

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page(s)

216-20

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cites work

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380010307

7 January 2021

The CpG dinucleotide and human genetic disease

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380010307

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380010307

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380010307

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380010307

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380010307

7 January 2021

Recurrent nonsense mutation in exon 7 of the phenylalanine hydroxylase gene

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380010307

7 January 2021

Characteristics of Mongoloid and neighboring populations based on the genetic markers of human immunoglobulins

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380010307

7 January 2021

A prevalent missense mutation in Northern Europe associated with hyperphenylalaninaemia

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380010307

7 January 2021

Phenylketonuria missense mutations in the Mediterranean

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380010307

7 January 2021

Origin of the Koreans: a population genetic study

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380010307

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380010307

7 January 2021

Molecular genetics of PKU in eastern Europe: a nonsense mutation associated with haplotype 4 of the phenylalanine hydroxylase gene

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380010307

7 January 2021

Founder effect of a prevalent phenylketonuria mutation in the Oriental population

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380010307

7 January 2021

Determination of the mutations responsible for the Lesch-Nyhan syndrome in 17 subjects

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380010307

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380010307

7 January 2021

Gm and Km allotypes in 74 Chinese populations: a hypothesis of the origin of the Chinese nation

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380010307

7 January 2021

Identifiers

DOI

10.1002/HUMU.1380010307

0 references