(Q33958014)

30 July 2017

Phenylketonuria as a balanced polymorphism: the nature of the heterozygote advantage (English)

1 reference

30 July 2017

0 references

1 reference

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1190737

30 August 2022

1 reference

https://api.crossref.org/works/10.1111/J.1469-1809.1975.TB00635.X

24 October 2023

author name string

L. I. Woolf

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1190737

30 August 2022

M. S. McBean

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1190737

30 August 2022

F. M. Woolf

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1190737

30 August 2022

S. F. Cahalane

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1190737

30 August 2022

language of work or name

English

0 references

publication date

1 May 1975

1 reference

full work available at URL

30 July 2017

https://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1111%2Fj.1469-1809.1975.tb00635.x

1 reference

https://api.crossref.org/works/10.1111/J.1469-1809.1975.TB00635.X

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1469-1809.1975.tb00635.x/fullpdf

24 October 2023

1 reference

https://api.crossref.org/works/10.1111/J.1469-1809.1975.TB00635.X

24 October 2023

published in

Annals of Human Genetics

1 reference

30 July 2017

38

1 reference

30 July 2017

4

1 reference

30 July 2017

461-469

1 reference

Maternal phenylketonuria: implications for growth and development

30 July 2017

1 reference

https://api.crossref.org/works/10.1111%2FJ.1469-1809.1975.TB00635.X

Children of mothers with phenylketonuria

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1469-1809.1975.TB00635.X

Genetics of Phenylketonuria: Heterozygosity for phenylketonuria

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1469-1809.1975.TB00635.X

Causes for high phenylalanine with normal tyrosine in newborn screening programs

21 January 2018

2

1 reference

https://api.crossref.org/works/10.1111/J.1469-1809.1975.TB00635.X

Phenylketonuria. Mass screening of newborns in Ireland

24 October 2023

5

1 reference

https://api.crossref.org/works/10.1111/J.1469-1809.1975.TB00635.X

The birthplaces of parents and grandparents of a series of patients with phenylketonuria in in south-east England

24 October 2023

6

1 reference

https://api.crossref.org/works/10.1111/J.1469-1809.1975.TB00635.X

Phenylalanine-hydroxylase activity in hyperphenylalaninaemia

24 October 2023

18

1 reference

https://api.crossref.org/works/10.1111/J.1469-1809.1975.TB00635.X

MATERNAL PHENYLKETONURIA. A CAUSE OF MENTAL RETARDATION IN CHILDREN WITHOUT THE METABOLIC DEFECT.

24 October 2023

23

1 reference

https://api.crossref.org/works/10.1111/J.1469-1809.1975.TB00635.X

Phenylketonuria; a problem in eugenics

24 October 2023

24

1 reference

https://api.crossref.org/works/10.1111/J.1469-1809.1975.TB00635.X

24 October 2023

31

139

740

Woo S. L.-C

1974

1 reference

https://api.crossref.org/works/10.1111/J.1469-1809.1975.TB00635.X

A third allele at the phenylalanine-hydroxylase locus in mild phenylketonuria (hyperphenylalaninaemia)

24 October 2023

34

1 reference

https://api.crossref.org/works/10.1111/J.1469-1809.1975.TB00635.X

24 October 2023

Identifiers

1 reference

30 July 2017

1 reference