Browsing by Subject Genetics -- Malta
Showing results 1 to 13 of 13
| Issue Date | Title | Author(s) |
| 2023 | Genetic landscape of ALS in Malta based on a quinquennial analysis | Farrugia Wismayer, Maria; Farrugia Wismayer, Andrew; Borg, Rebecca; Abela, André; Chircop, Charmaine; Aquilina, Josanne; Soler, Doriette; Pace, Adrian; Vella, Malcolm; Vassallo, Neville; Cauchi, Ruben J.; Bonavia, Karl |
| 2012 | Genetic predisposition and functional analysis of pituitary adenomas | Formosa, Robert |
| 2019 | The genetic side of type 2 diabetes – a review | Cuschieri, Sarah |
| 1999 | Genetics : a multimedia software package | Casaru, Anthony; Debono, Elaine |
| 2017 | Genetics in midwifery : exploring the midwives’ views and educational needs in clinical practice | Cassar, Catriona |
| 2022 | Genetics of autosomal dominant polycystic kidney disease | Zammit, Jeremy (2022) |
| 2024 | Genotype-phenotype of autosomal dominant polycystic kidney disease in Malta | Ciantar, Natalie; Zahra, Graziella; Delicata, Julian; Sammut, Fiona; Calleja-Agius, Jean; Farrugia, Emanuel; Said, Edith |
| 2022 | Identification of genetic determinants underlying familial osteoporosis | Dalli, Karl (2022) |
| 2023 | Identifying a genetic association between non-autoimmune diabetes & bone mass | Mangion, Darren (2023) |
| 2019 | Identifying mutations causing sarcomeric hypertrophic cardiomyopathy in the Maltese population | Felica, Tiziana |
| 2019 | Local allele frequencies of the 5-HTTLPR serotonin transporter promoter polymorphism | Grech, Christopher; Bezzina Wettinger, Stephanie; Farrugia, Rosienne |
| 2022 | The use of high throughput sequencing for the identification of variants contributing to Hirschsprung disease in the Maltese | Gatt, Veronique (2022) |
| 2022 | Variants in STAT4 and TMEM151B identified as potential causal factors in early-onset familial osteoporosis | Schembri, Marichela; Friggieri, Donald; Vassallo, Josanne; Xuereb-Anastasi, Angela; Formosa, Melissa Marie |
