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Phenylketonuria as a balanced polymorphism: the nature of the heterozygote advantage.
Ann Hum Genet. 1975 May;38(4):461-9. doi: 10.1111/j.1469-1809.1975.tb00635.x.
Ann Hum Genet. 1975.
PMID: 1190737
Birth weight and pathogenesis in phenylketonuria.
Crockett DJ, Woolf LI, McBean MS, Woolf FM, Cahalane SF.
Crockett DJ, et al. Among authors: mcbean ms.
Int J Neurosci. 1990 Oct;54(3-4):259-66. doi: 10.3109/00207459008986642.
Int J Neurosci. 1990.
PMID: 2265974
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A third allele at the phenylalanine-hydroxylase locus in mild phenylketonuria (hyperphenylalaninaemia).
Woolf LI, Goodwin BL, Cranston WI, Wade DN, Woolf F, Hudson FP, McBean MS.
Woolf LI, et al. Among authors: mcbean ms.
Lancet. 1968 Jan 20;1(7534):114-7. doi: 10.1016/s0140-6736(68)92722-0.
Lancet. 1968.
PMID: 4169602
No abstract available.
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Treatment of classical phenylketonuria.
MCBean MS, Stephenson JB.
MCBean MS, et al.
Arch Dis Child. 1968 Feb;43(227):1-7. doi: 10.1136/adc.43.227.1.
Arch Dis Child. 1968.
PMID: 4868338
Free PMC article.
Clinical Trial.
No abstract available.
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Diagnosis of phenylketonuria (phenylalanine hydroxylase deficiency, temporary and permanent).
Stephenson JB, McBean MS.
Stephenson JB, et al. Among authors: mcbean ms.
Br Med J. 1967 Sep 2;3(5565):579-81. doi: 10.1136/bmj.3.5565.579.
Br Med J. 1967.
PMID: 20791345
Free PMC article.
No abstract available.
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Phenylketonuria: a reassessment of mass infant screening by napkin test.
Stephenson JB, McBean MS.
Stephenson JB, et al. Among authors: mcbean ms.
Br Med J. 1967 Sep 2;3(5565):582. doi: 10.1136/bmj.3.5565.582.
Br Med J. 1967.
PMID: 20791346
Free PMC article.
No abstract available.
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