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Search Results - Schoonheyt, W.E.
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“Hypotyrosinemia” in Phenylketonuria
by
Hanley, W.B.
,
Lee, A.W.
,
Hanley, A.J.G.
,
Lehotay, D.C.
,
Austin, V.J.
,
Schoonheyt, W.E.
,
Platt, B.A.
,
Clarke, J.T.R.
Published in
Molecular genetics and metabolism
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Newborn phenylketonuria (PKU) Guthrie (BIA) screening and early hospital discharge
by
Hanley, W.B.
,
Demshar, H.
,
Preston, M.A.
,
Borczyk, A.
,
Schoonheyt, W.E.
,
Clarke, J.T.R.
,
Feigenbaum, A.
Published in
Early human development
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Maternal Phenylketonuria (MPKU)
by
Schoonheyt, W E
,
Hanley, W B
,
Clarke, J T
,
Austin, V
,
Howe, D A
Published in
Canadian family physician
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Canadian Family Physician
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Early Human Development
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Molecular Genetics And Metabolism
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Humans
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Infant, Newborn
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Life Sciences & Biomedicine
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Phenylalanine - Blood
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Phenylketonuria
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Phenylketonurias - Blood
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Adolescent
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Analysis Of Variance
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Bacterial Inhibition Assay - Guthrie Test Method
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Bacterial Inhibition Assay — Guthrie Test Method
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Early Newborn Discharge
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Endocrinology & Metabolism
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False Negative Reactions
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Family Practice Case Book
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