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Results of search for 'au:"Naughton, E"'
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Authors
Beighi, B
Burke, J
Chakraborty, R
Dasovich, M
Eisensmith, R C
Giovannini, M
Goltsov, A A
Güttler, F
Jin, L
Konecki, D
Lichter-Konecki, U
Mullins, C
Naughton, E
Naughton, E R
O'Keefe, M
Riva, E
Taylor, R H
Woo, S L
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Adolescent
Adult
Age Factors
Alleles
Base Sequence
Child
Child, Preschool
DNA
DNA Probes
Female
Follow-Up Studies
Gene Frequency
Genetic Carrier Screening
Genotype
Humans
Molecular Sequence Data
Phenylalanine Hydroxylase
Phenylketonurias
diagnosis
genetics
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Your search returned 3 results.
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1.
Ophthalmic abnormalities in homocystinuria: the value of screening.
[electronic resource]
by
Taylor, R H
Burke, J
O'Keefe, M
Beighi, B
Naughton, E
Producer:
19981030
In:
Eye (London, England)
vol. 12 ( Pt 3a)
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2.
A single polymorphic STR system in the human phenylalanine hydroxylase gene permits rapid prenatal diagnosis and carrier screening for phenylketonuria.
[electronic resource]
by
Goltsov, A A
Eisensmith, R C
Naughton, E R
Jin, L
Chakraborty, R
Woo, S L
Producer:
19930727
In:
Human molecular genetics
vol. 2
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3.
Molecular characterization of PKU allele prevalent in southern Europe and Ireland.
[electronic resource]
by
Dasovich, M
Konecki, D
Lichter-Konecki, U
Eisensmith, R C
Güttler, F
Naughton, E
Mullins, C
Giovannini, M
Riva, E
Woo, S L
Producer:
19910717
In:
Somatic cell and molecular genetics
vol. 17
Online resources:
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