Literature DB >> 3093157

Newborn screening for phenylketonuria in eleven districts.

S R Liu, Q H Zuo.   

Abstract

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Year:  1986        PMID： 3093157

Source DB:  PubMed          Journal:  Chin Med J (Engl)        ISSN： 0366-6999            Impact factor:   2.628


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  8 in total

1.  Protein stability and in vivo concentration of missense mutations in phenylalanine hydroxylase.

Authors:  Zhen Shi; Jenn Sellers; John Moult
Journal:  Proteins       Date:  2011-09-21

Review 2.  Paediatric illness in Hong Kong and Britain.

Authors:  D P Davies
Journal:  Arch Dis Child       Date:  1992-04       Impact factor: 3.791

3.  The molecular basis of phenylketonuria in Koreans.

Authors:  Dong Hwan Lee; Soo Kyung Koo; Kwang-Soo Lee; Young-Joo Yeon; Hyun-Jeong Oh; Sang-Wun Kim; Sook-Jin Lee; Sung-Soo Kim; Jong-Eun Lee; Inho Jo; Sung-Chul Jung
Journal:  J Hum Genet       Date:  2004-10-16       Impact factor: 3.172

Review 4.  Why are some genetic diseases common? Distinguishing selection from other processes by molecular analysis of globin gene variants.

Authors:  J Flint; R M Harding; J B Clegg; A J Boyce
Journal:  Hum Genet       Date:  1993-03       Impact factor: 4.132

5.  Multiple origins for phenylketonuria in Europe.

Authors:  R C Eisensmith; Y Okano; M Dasovich; T Wang; F Güttler; H Lou; P Guldberg; U Lichter-Konecki; D S Konecki; E Svensson
Journal:  Am J Hum Genet       Date:  1992-12       Impact factor: 11.025

6.  Birth prevalence of phenylalanine hydroxylase deficiency: a systematic literature review and meta-analysis.

Authors:  Pamela K Foreman; Andrea V Margulis; Kimberly Alexander; Renee Shediac; Brian Calingaert; Abenah Harding; Manel Pladevall-Vila; Sarah Landis
Journal:  Orphanet J Rare Dis       Date:  2021-06-03       Impact factor: 4.123

7.  Global prevalence of classic phenylketonuria based on Neonatal Screening Program Data: systematic review and meta-analysis.

Authors:  Hamid Reza Shoraka; Ali Akbar Haghdoost; Mohammad Reza Baneshi; Zohre Bagherinezhad; Farzaneh Zolala
Journal:  Clin Exp Pediatr       Date:  2020-02-06

8.  Rapid single-base mismatch detection in genotyping for phenylketonuria.

Authors:  Yutaka Takarada; Shohei Kagawa; Yoshiyuki Okano; Takakuni Tanizawa
Journal:  Mol Biotechnol       Date:  2003-07       Impact factor: 2.860
  8 in total

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