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Bezzina, Alex
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1

Restoring Africa's Lions: Start With Good Counts:

Braczkowski, Alex ; Gopalaswamy, Arjun M. ; Elliot, Nicholas B....
Frontiers in Ecology and Evolution.  8 (2020)  - p. , 2020
Link: https://doi.org/10.3389/..
 
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2

A New Footbridge in Valletta Grand Harbour to Fill A Geomet..:

Pereda, Héctor Beade ; Miguel, Guillermo Capellán ; Bezzina, Alex...
Structural Engineering International.  25 (2015)  2 - p. 213-217 , 2015
Link: https://doi.org/10.2749/..
 
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3

Image_1_Restoring Africa's Lions: Start With Good Counts.pd:

Alex Braczkowski ; Arjun M. Gopalaswamy ; Nicholas B. Elliot...
doi:10.3389/fevo.2020.00138.s001.  , 2020
Link: https://doi.org/10.3389/..
 
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4

Restoring Africa's Lions: Start With Good Counts:

Alex Braczkowski ; Arjun M. Gopalaswamy ; Nicholas B. Elliot...
https://www.frontiersin.org/article/10.3389/fevo.2020.00138/full.  , 2020
Link: https://doi.org/10.3389/..
 
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5

A Single Na+Channel Mutation Causing Both Long-QT and Bruga..:

Bezzina, Connie ; Veldkamp, Marieke W. ; van den Berg, Maarten P....
Circulation Research.  85 (1999)  12 - p. 1206-1213 , 1999
Link: https://doi.org/10.1161/..
 
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6

Exploring the complex spectrum of dominance and recessivene..:

Lipov, Alex ; Jurgens, Sean J. ; Mazzarotto, Francesco...
Nature Cardiovascular Research.  2 (2023)  11 - p. 1078-1094 , 2023
Link: https://doi.org/10.1038/..
 
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7

Common genetic variants improve risk stratification after t..:

Woudstra, Odilia I. ; Skoric-Milosavljevic, Doris ; Mulder, Barbara J.M....
International Journal of Cardiology.  371 (2023)  - p. 153-159 , 2023
Link: https://doi.org/10.1016/..
 
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8

GATA6 mutations: Characterization of two novel patients and..:

Škorić‐Milosavljević, Doris ; Tjong, Fleur V. Y. ; Barc, Julien...
American Journal of Medical Genetics Part A.  179 (2019)  9 - p. 1836-1845 , 2019
Link: https://doi.org/10.1002/..
 
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9

Homozygous frameshift mutations in FAT1 cause a syndrome ch..:

Lahrouchi, Najim ; George, Aman ; Ratbi, Ilham...
Nature Communications.  10 (2019)  1 - p. , 2019
Link: https://doi.org/10.1038/..
 
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10

Exome sequencing identifies primary carnitine deficiency in..:

Lahrouchi, Najim ; Lodder, Elisabeth M ; Mansouri, Maria...
European Journal of Human Genetics.  25 (2017)  6 - p. 783-787 , 2017
Link: https://doi.org/10.1038/..
 
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11

Genetic causes of Parkinson's disease in the Maltese: a stu..:

Zahra, Charmaine ; Tabone, Christine ; Camilleri, Graziella...
BMC Medical Genetics.  17 (2016)  1 - p. , 2016
Link: https://doi.org/10.1186/..
 
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12

Genetics of congenital heart disease: the contribution of t..:

Postma, Alex V ; Bezzina, Connie R ; Christoffels, Vincent M
Journal of Human Genetics.  61 (2015)  1 - p. 13-19 , 2015
Link: https://doi.org/10.1038/..
 
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13

Identification of FOXP1 deletions in three unrelated patien..:

Horn, Denise ; Kapeller, Johannes ; Rivera-Brugués, Núria...
Human Mutation.  31 (2010)  11 - p. E1851-E1860 , 2010
Link: https://doi.org/10.1002/..
 
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14

Genomic organisation and chromosomal localisation of two me..:

Postma, Alex V. ; Bezzina, Connie R. ; de Vries, Jeltje F....
Human Genetics.  106 (2000)  6 - p. 614-619 , 2000
Link: https://doi.org/10.1007/..
 
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15

[Gabra ta' kitbiet : Lehen il-Malti, Ghadd 33] (2014). Kalm..:

Cassar, Antoine ; Camilleri, Charló ; Saliba, Rita...
[Gabra ta' kitbiet : Lehen il-Malti, Ghadd 33] (2014). Kalm.  , 2014
Link: https://www.um.edu.mt/li..
 
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