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Results of search for 'au:"de la Fuente Juárez, A"'
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Authors
Campistol Plana, J
Capdevila Cogul, E
Muñoz Prades, A
Porta Ribera, R
Sánchez Pozón, L
Viñallonga Sardà, X
de la Fuente Juárez, A
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Topics
Brain Diseases
Calcinosis
Female
Glucuronosyltransferase
Humans
Hyperbilirubinemia, Neonatal
Infant, Newborn
Mutation
Psychomotor Disorders
Syndrome
Time Factors
diagnosis
genetics
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Spanish
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1.
[Prolonged neonatal hyperbilirubinemia associated with a UGT1A1 gene mutation].
[electronic resource]
by
de la Fuente Juárez, A
Viñallonga Sardà, X
Capdevila Cogul, E
Porta Ribera, R
Producer:
20101124
In:
Anales de pediatria (Barcelona, Spain : 2003)
vol. 72
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Available from publisher's website
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2.
[Aicardi-Goutières syndrome].
[electronic resource]
by
de la Fuente Juárez, A
Sánchez Pozón, L
Muñoz Prades, A
Campistol Plana, J
Porta Ribera, R
Producer:
20080529
In:
Anales de pediatria (Barcelona, Spain : 2003)
vol. 68
Online resources:
Available from publisher's website
Availability:
No items available.
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(remove)