Literature DB >> 13691132

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

C O CARTER, L I WOOLF.   

Abstract

Entities:  

Keywords:  PHENYLPYRUVIC OLIGOPHRENIA/genetics

Mesh：

Year:  1961        PMID： 13691132     DOI： 10.1111/j.1469-1809.1961.tb01497.x

Source DB:  PubMed          Journal:  Ann Hum Genet        ISSN： 0003-4800            Impact factor:   1.670


× No keyword cloud information.
  10 in total

1.  Infantile cystinosis in France: genetics, incidence, geographic distribution.

Authors:  E Bois; J Feingold; P Frenay; M L Briard
Journal:  J Med Genet       Date:  1976-12       Impact factor: 6.318

2.  Genetic study of Welsh gypsies.

Authors:  E M Williams; P R Harper
Journal:  J Med Genet       Date:  1977-06       Impact factor: 6.318

3.  The heterozygote advantage in phenylketonuria.

Authors:  L I Woolf
Journal:  Am J Hum Genet       Date:  1986-05       Impact factor: 11.025

4.  Risk of anenceply in migrant and non-migrant women in the Oxford area.

Authors:  M S Hobbs
Journal:  Br J Prev Soc Med       Date:  1969-08

5.  Phenylketonuria. Mass screening of newborns in Ireland.

Authors:  S F Cahalane
Journal:  Arch Dis Child       Date:  1968-04       Impact factor: 3.791

6.  Mass screening of the newborn for metabolic disease.

Authors:  L I Woolf
Journal:  Arch Dis Child       Date:  1968-04       Impact factor: 3.791

Review 7.  The phenylketonuria locus: current knowledge about alleles and mutations of the phenylalanine hydroxylase gene in various populations.

Authors:  D S Konecki; U Lichter-Konecki
Journal:  Hum Genet       Date:  1991-08       Impact factor: 4.132

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

Authors:  S P Daiger; R Chakraborty; L Reed; G Fekete; D Schuler; G Berenssi; I Nasz; R Brdicka; J Kamarýt; A Pijácková
Journal:  Am J Hum Genet       Date:  1989-08       Impact factor: 11.025

9.  Present status of different mass screening procedures for phenylketonuria. Medical Research Council Working Party on phenylketonuria.

Authors: 
Journal:  Br Med J       Date:  1968-10-05

10.  Genetic variation in Wales.

Authors:  P S Harper
Journal:  J R Coll Physicians Lond       Date:  1976-07
  10 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.