(Q41342853)

29 September 2017

title

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

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29 September 2017

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Güttler F

1

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29 September 2017

Ledley FD

2

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29 September 2017

Lidsky AS

3

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29 September 2017

DiLella AG

4

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29 September 2017

Sullivan SE

5

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29 September 2017

Woo SL

6

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29 September 2017

language of work or name

English

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publication date

1 January 1987

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The Journal of Pediatrics

29 September 2017

published in

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29 September 2017

volume

110

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29 September 2017

issue

1

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29 September 2017

page(s)

68-71

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Phenylketonuria: epitome of human biochemical genetics (first of two parts).

29 September 2017

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2887%2980290-1

Phenylketonuria and other phenylalanine hydroxylation mutants in man.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2887%2980290-1

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2887%2980290-1

Gene transfer and expression of human phenylalanine hydroxylase

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2887%2980290-1

Molecular structure and polymorphic map of the human phenylalanine hydroxylase gene

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2887%2980290-1

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2887%2980290-1

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2887%2980290-1

Prenatal diagnosis of classic phenylketonuria by DNA analysis

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2887%2980290-1

The morbid anatomy of the human genome: a review of gene mapping in clinical medicine (1).

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2887%2980290-1

Heterogeneity in Genetic Control of Phenylalanine Metabolism in Man

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2887%2980290-1

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2887%2980290-1

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2887%2980290-1

10.1016/S0022-3476(87)80290-1

7 January 2021

Identifiers

DOI

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29 September 2017

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