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Human Phenylalanine Hydroxylase Mutations and Hyperphenylalaninemia Phenotypes: A Metanalysis of Genotype-Phenotype Correlations

American journal of human genetics, 1997-12, Vol.61 (6), p.1309-1317

1997

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PAH Mutation Analysis Consortium Database: a database for disease-producing and other allelic variation at the human PAH locus

Nucleic acids research, 1996-01, Vol.24 (1), p.127

1996

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PAH Mutation Analysis Consortium Database: 1997. Prototype for relational locus-specific mutation databases

Nucleic acids research, 1998-01, Vol.26 (1), p.220

1998

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The PAH mutation analysis consortium database: update 1996

Nucleic acids research, 1997-01, Vol.25 (1), p.139

1997

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Evidence for origin, by recurrent mutation, of the phenylalanine hydroxylase R408W mutation on two haplotypes in European and Quebec populations

Human molecular genetics, 1994-09, Vol.3 (9), p.1675-1677

1994

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Prediction of multiple hypermutable codons in the human PAH gene: Codon 280 contains recurrent mutations in Quebec and other populations

Human mutation, 1997, Vol.9 (4), p.316-321

1997

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Mutation at the phenylalanine hydroxylase gene (PAH) and its use to document population genetic variation: the Quebec experience

European journal of human genetics : EJHG, 1998-01, Vol.6 (1), p.61-70

1998

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Cross-correctional studies in inborn errors of vitamin B12 metabolism

Byck, Susan

1989

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ProQuest

The Phenylalanine Hydroxylase Locus: A Marker for the History of Phenylketonuria and Human Genetic Diversity

Ciba Foundation Symposium 197 ‐ Variation in the Human Genome, 2007, p.73-96

2007

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Evaluation of a Prospective Payment System for VA Contract Nursing Homes

Evaluation & the health professions, 1996-12, Vol.19 (4), p.423-442

1996

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WHAT IT'S LIKE TO BE A WOMAN IN WASHINGTON

The Washingtonian (Washington, D.C.), 2019-10, Vol.55 (1), p.55

2019

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Human Phenylalanine Hydroxylase Mutations and Hyperphenylalaninemia Phenotypes: A Metanalysis of Genotype-Phenotype Correlations

Genetic diversity within the R408W phenylketonuria mutation lineages in Europe

PAH Mutation Analysis Consortium Database: a database for disease-producing and other allelic variation at the human PAH locus

PAH Mutation Analysis Consortium Database: 1997. Prototype for relational locus-specific mutation databases

The PAH mutation analysis consortium database: update 1996

Evidence for origin, by recurrent mutation, of the phenylalanine hydroxylase R408W mutation on two haplotypes in European and Quebec populations

Prediction of multiple hypermutable codons in the human PAH gene: Codon 280 contains recurrent mutations in Quebec and other populations

Mutation at the phenylalanine hydroxylase gene (PAH) and its use to document population genetic variation: the Quebec experience

Cross-correctional studies in inborn errors of vitamin B12 metabolism

The Phenylalanine Hydroxylase Locus: A Marker for the History of Phenylketonuria and Human Genetic Diversity

Evaluation of a Prospective Payment System for VA Contract Nursing Homes

WHAT IT'S LIKE TO BE A WOMAN IN WASHINGTON

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