Literature DB >> 5022449

Problems in the biochemical detection of heterozygotes for phenylketonuria.

L Y Yakymyshyn, D W Reid, D J Campbell.   

Abstract

Entities:  

Mesh：

Substances：

Year:  1972        PMID： 5022449     DOI： 10.1016/s0009-9120(72)80010-9

Source DB:  PubMed          Journal:  Clin Biochem        ISSN： 0009-9120            Impact factor:   3.281


× No keyword cloud information.
  5 in total

1.  Heterozygote detection in phenylketonuria. Measurement of discriminatory ability and interpretation of the phenylalanine loading test by determination of the heterozygote likelihood ratio.

Authors:  A Westwood; D N Raine
Journal:  J Med Genet       Date:  1975-12       Impact factor: 6.318

2.  Classic phenylketonuria: heterozygote detection during pregnancy.

Authors:  R F Griffin; M E Humienny; E C Hall; L J Elsas
Journal:  Am J Hum Genet       Date:  1973-11       Impact factor: 11.025

3.  Phenylketonuria heterozygote detection in families with affected children.

Authors:  T D Paul; I K Brandt; L J Elsas; C E Jackson; P Mamunes; C S Nance; W E Nance
Journal:  Am J Hum Genet       Date:  1978-05       Impact factor: 11.025

4.  Improved identification of heterozygotes for phenylketonuria using blood neopterin and biopterin.

Authors:  T Alós; Y Bel; M L Cabello; J L Catalá; J Dalmau; J Ferré; A M García; P Ruiz-Vázquez
Journal:  J Inherit Metab Dis       Date:  1993       Impact factor: 4.982

5.  Carrier screening for phenylketonuria: comparison of two discriminant analysis procedures.

Authors:  C L Freehauf; D Lezotte; S I Goodman; E R McCabe
Journal:  Am J Hum Genet       Date:  1984-11       Impact factor: 11.025
  5 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.