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Case fatality rate and associated factors in patients with 22q11 microdeletion syndrome: a retrospective cohort study. [electronic resource] by
- Repetto, Gabriela M
- Guzmán, M Luisa
- Delgado, Iris
- Loyola, Hugo
- Palomares, Mirta
- Lay-Son, Guillermo
- Vial, Cecilia
- Benavides, Felipe
- Espinoza, Karena
- Alvarez, Patricia
Producer: 20150702
In:
BMJ open vol. 4
Availability: No items available.
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19.
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Accuracy of a Genetic Test for the Diagnosis of Hypolactasia in Chilean Children: Comparison With the Breath Test. [electronic resource] by
- Alliende, Francisco
- Vial, Cecilia
- Espinoza, Karen
- Schnettle, Daniela
- Romero, Victoria
- Miquel, Isabel
- Arancibia, Maria E
- Rios, Gloria
- Rodriguez, Lorena
- Quesada, Soledad
- Lucero, Yalda
- Repetto, Gabriela M
Producer: 20180109
In:
Journal of pediatric gastroenterology and nutrition vol. 63
Availability: No items available.
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20.
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A combined syndrome of juvenile polyposis and hereditary haemorrhagic telangiectasia associated with mutations in MADH4 (SMAD4). [electronic resource] by
- Gallione, Carol J
- Repetto, Gabriela M
- Legius, Eric
- Rustgi, Anil K
- Schelley, Susan L
- Tejpar, Sabine
- Mitchell, Grant
- Drouin, Eric
- Westermann, Cornelius J J
- Marchuk, Douglas A
Producer: 20040419
In:
Lancet (London, England) vol. 363
Availability: No items available.
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