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Browsing by Author Said, Edith

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Issue DateTitleAuthor(s)
2004Defect in dorso-ventral patterning, asplenia, and conotruncus in a spontaneously aborted fetusCuschieri, Alfred; Said, Edith; Calleja-Agius, Jean
2018Diagnosis of mitochondrial disorders by whole exome sequencingVella, Joanna; Laurie, S.; Borg, Joseph J.; Soler, Doriette; Vella, Norbert; Aquilina, Josanne; Said, Edith; Borg, Isabella; Felice, Alex E.
2017DiGeorge phenotype in the absence of 22q11 deletion : a case reportTaliana, Nikita; Said, Edith; Grech, Victor E.
2024Genotype-phenotype of autosomal dominant polycystic kidney disease in MaltaCiantar, Natalie; Zahra, Graziella; Delicata, Julian; Sammut, Fiona; Calleja-Agius, Jean; Farrugia, Emanuel; Said, Edith
2018Malta BioBank (BBMRI.mt) in RD-ConnectVella, Joanna; Soler, Doriette; Scerri, Christian A.; Vella, Norbert; Aquilina, Josanne; Borg, Isabella; Said, Edith; Spiteri, A.; Dalli, J.; Ryabova, L.; Pace, Malcolm; Borg, Joseph J.; Grech, Laura; Camilleri, Alexander; Zammit, E.; Said-Conti, V.; Pace, N.; Vassallo, Josanne; Felice, Alex E.
2009Molecular cytogenetics in the diagnosis of mental retardation in MaltaSaid, Edith
2020Neuropsychosocial outcomes of patients with untreated craniosynostosisAttard Mallia, Tamara; Said, Edith
2000A population study of FMR1 mutations in MaltaSaid, Edith
2015-03Rare disease research and the Malta biobankVella, Joanna; Borg, Joseph J.; Grech, Laura; Galdies, Ruth; Scerri, Jeanesse; Cassar, Wilhelmina; Scerri, Christian A.; Grech, Godfrey; Soler, Doriette; Said, Edith; Borg, Isabella; Vella, Norbert; Camilleri-Podesta, Marie Therese; Ellul, Bridget; Abela, Mark; Grima, David; Zammit, Esther; Pace, Nikolai Paul; Felice, Alex; Said Conti, Valerie
2016Y chromosome in turner syndrome : a case reportTaliana, Nikita; Grech, Victor E.; DeGiovanni, Joseph V.; Said, Edith
Showing results 4 to 13 of 13 < previous