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KORKMAZ, HUSEYIN A [Author]
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Katipoğlu, Nagehan et al.
Síndrome de anemia megaloblástica sensible a la tiamina de aparición en la niñez, con mutación en el genSLC19A2: caso clínico
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Arch. argent. pediatr.
, Jun 2017, vol.115, no.3, p.e153-e156. ISSN 0325-0075
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Hazan, Filiz et al.
Niño con síndrome tricorrinofalángico tipo II acompañado de baja estatura
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Arch. argent. pediatr.
, Dic 2016, vol.114, no.6, p.e403-e407. ISSN 0325-0075
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Korkmaz, Hüseyin A et al.
Asociación entre el síndrome de Wolfram y la tetralogía de Fallot en una niña
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Arch. argent. pediatr.
, Jun 2016, vol.114, no.3, p.e163-e166. ISSN 0325-0075
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