Literature DB >> 6700105

Prenatal diagnosis of classical phenylketonuria by gene mapping.

S L Woo, A S Lidsky, F Güttler, C Thirumalachary, K J Robson.   

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Year:  1984        PMID： 6700105

Source DB:  PubMed          Journal:  JAMA        ISSN： 0098-7484            Impact factor:   56.272


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  5 in total

1.  Analysis of three restriction fragment length polymorphisms in the human type II procollagen gene.

Authors:  C E Eng; C M Strom
Journal:  Am J Hum Genet       Date:  1985-07       Impact factor: 11.025

2.  Recombinant DNA techniques in the diagnosis of inherited disorders.

Authors:  J F Gusella
Journal:  J Clin Invest       Date:  1986-06       Impact factor: 14.808

3.  Molecular genetics of PKU.

Authors:  F Güttler; S L Woo
Journal:  J Inherit Metab Dis       Date:  1986       Impact factor: 4.982

Review 4.  Genetics of gene expression in CNS.

Authors:  Ashutosh K Pandey; Robert W Williams
Journal:  Int Rev Neurobiol       Date:  2014       Impact factor: 3.230

5.  Regional mapping of the phenylalanine hydroxylase gene and the phenylketonuria locus in the human genome.

Authors:  A S Lidsky; M L Law; H G Morse; F T Kao; M Rabin; F H Ruddle; S L Woo
Journal:  Proc Natl Acad Sci U S A       Date:  1985-09       Impact factor: 11.205
  5 in total

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