Literature DB >> 8803787

Short tandem repeat polymorphisms in Japanese families with phenylketonuria.

Y Kang1, Y Okano, Y Hase, T Oura, G Isshiki.   

Abstract

Entities:  

Mesh：

Year:  1996        PMID： 8803787     DOI： 10.1007/bf01799274

Source DB:  PubMed          Journal:  J Inherit Metab Dis        ISSN： 0141-8955            Impact factor:   4.982


× No keyword cloud information.
  4 in total

1.  Mutation of human short tandem repeats.

Authors:  J L Weber; C Wong
Journal:  Hum Mol Genet       Date:  1993-08       Impact factor: 6.150

2.  A single polymorphic STR system in the human phenylalanine hydroxylase gene permits rapid prenatal diagnosis and carrier screening for phenylketonuria.

Authors:  A A Goltsov; R C Eisensmith; E R Naughton; L Jin; R Chakraborty; S L Woo
Journal:  Hum Mol Genet       Date:  1993-05       Impact factor: 6.150

3.  A simple, rapid, and highly informative PCR-based procedure for prenatal diagnosis and carrier screening of phenylketonuria.

Authors:  R C Eisensmith; A A Goltsov; S L Woo
Journal:  Prenat Diagn       Date:  1994-12       Impact factor: 3.050

4.  Frequency and distribution of phenylketonuric mutations in Orientals.

Authors:  Y Okano; Y Hase; D H Lee; J Furuyama; H Shintaku; T Oura; G Isshiki
Journal:  Hum Mutat       Date:  1992       Impact factor: 4.878
  4 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.