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Showing results 40 to 45 of 45
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Issue Date
Title
Author(s)
2020
Rare variant burden analysis within enhancers identifies CAV1 as an ALS risk gene
Cooper-Knock, Johnathan
;
Zhang, Sai
;
Kenna, Kevin P.
;
Moll, Tobias
;
Franklin, John P.
;
Allen, Samantha
;
Ghahremani Nezhad, Helia
;
Iacoangeli, Alfredo
;
Yacovzada, Nancy Y.
;
Eitan, Chen
;
Hornstein, Eran
;
Elhaik, Eran
;
Celadova, Petra
;
Bose, Daniel
;
Farhan, Sali
;
Fishilevich, Simon
;
Lancet, Doron
;
Morrison, Karen E.
;
Shaw, Christopher E.
;
Al-Chalabi, Ammar
;
Veldink, Jan H.
;
Kirby, Janine
;
Snyder, Michael P.
;
Shaw, Pamela J.
;
Cauchi, Ruben J.
;
Project MinE ALS Sequencing Consortium
2018
The role of FLVCR1 isoforms on inter-erythrocytic distribution of human foetal haemoglobin
Grech, Laura
;
Scerri, Jeanesse
;
Mizzi, Clint
;
Galdies, Ruth
;
Scerri, Christian A.
;
Ijcken, Wilfred van
;
Özgür, Zeliha
;
Gillemans, Nynke
;
Borg, Joseph J.
;
Philipsen, Sjaak
;
Felice, Alex E.
2022
Role of the RUNX2 rs59983488 variant in bone mass determination and fracture risk in Malta
Sammut, Nigel (2022)
2008
Sequencing of genes in two Maltese families with severe osteoporosis
Cachia, Adela
2019
Two novel GJA1 variants in oculodentodigital dysplasia
Pace, Nikolai Paul
;
Benoit, Valerie
;
Agius, David
;
Grima, Maria Angela
;
Parascandalo, Raymond
;
Hilbert, Pascale
;
Borg, Isabella
2008
Xjenza madwarna 1 : programs 1-18
Bugeja, Christopher