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Browsing by Author Cassar, Wilhelmina
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Showing results 5 to 14 of 14
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Issue Date
Title
Author(s)
2010
Haploinsufficiency for the erythroid transcription factor KLF1 causes hereditary persistence of fetal hemoglobin
Borg, Joseph J.
;
Papadopoulos, Petros
;
Georgitsi, Marianthi
;
Gutierrez, Laura
;
Grech, Godfrey
;
Fanis, Pavlos
;
Phylactides, Marios
;
Verkerk, Annemieke J.M.H.
;
van der Spek, Peter J.
;
Scerri, Christian A.
;
Cassar, Wilhelmina
;
Galdies, Ruth
;
van IJcken, Wilfred
;
Ozgur, Zeliha
;
Gillemans, Nynke
;
Hou, Jun
;
Bugeja, Marisa
;
Grosveld, Frank G.
;
von Lindern, Marieke
;
Felice, Alex
;
Patrinos, George P.
;
Philipsen, Sjaak
2018
Hb F Malta 1 : a biomarker for the developmental control of globin gene switching
Camilleri, Alexander
;
Galdies, Ruth
;
Cassar, Wilhelmina
;
Grech, Laura
;
Ebejer, Jean Paul
;
Borg, Joseph J.
;
Scerri, Christian A.
;
Felice, Alex E.
2010
Hb Valletta [β87 (F3) Thr→ Pro] and Hb Marseille/Long Island [β2 (NA2) His→ Pro;(–1) Met-(+ 1) Val-(+ 2) Pro-Leu], in a unique compound heterozygote with a normal hemoglobin phenotype
Galdies, Ruth
;
Cassar, Wilhelmina
;
Pizzuto, Monica
;
Scerri, Christian A.
;
Felice, Nicholas
;
Cassar, Olivianne A.
;
Buttigieg, George
;
Felice, Alex
2015
Large deletion in the EPCAM gene responsible for the milder phenotype of congenital tufting enteropathy
Gerada, Jurgen
;
Saliba, Christian
;
Galdies, Ruth
;
Cassar, Wilhelmina
;
Mercieca, Victor
;
DeGaetano, James
;
Gerada, Eleanor
;
Sebire, Neil
;
Hill, Susan
;
LaFerla, Godfrey
;
Vassallo, Mario
;
Scerri, Christian
;
Grech, Godfrey
;
Attard, Thomas M.
2014
Large deletion in the EPCAM gene responsible for the milder phenotype of congenital tufting enteropathy
Gerada, Jurgen
;
Saliba, Christian
;
Galdies, Ruth
;
Cassar, Wilhelmina
;
Mercieca, Victor
;
DeGaetano, James
;
Gerada, Eleanor
;
Sebire, Neil J.
;
Hill, Susan
;
Vassallo, Mario
;
Scerri, Christian A.
;
Grech, Godfrey
;
Attard, Thomas
2018
Novel beta globin gene cluster rearrangements and deletions in the Maltese islands
Camilleri, Alexander
;
Galdies, Ruth
;
Cassar, Wilhelmina
;
Grech, Laura
;
Borg, Joseph J.
;
Scerri, Christian A.
;
Felice, Alex E.
2012
Optimization of an imaging cytometry protocol to observe the cellular distribution of haemoglobin F in F-erythrocytes
Scerri, Jeanesse
;
Felice, Alex
;
Cassar, Wilhelmina
;
Scerri, Christian A.
;
Grech, Godfrey
;
Galdies, Ruth
;
Borg, Joseph J.
;
Saliba, Christian
2015-03
Rare disease research and the Malta biobank
Vella, 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
2007
A review of cis-trans interplay between DNA sequences 5′ to the Gγ-and β-globin genes among Hb F-Malta-I heterozygotes/homozygotes and β-thalassemia homozygotes/compound heterozygotes, and the effects of hydroxyurea on the Hb F/F-erythrocyte; the need for large multicenter trials
Felice, Alex
;
Borg, Joseph J.
;
Pizzuto, Monica
;
Cassar, Wilhelmina
;
Galdies, Ruth
;
Bezzina Wettinger, Stephanie
;
Pulis, Svetlana
;
Hunter, Gary J.
;
Caruana, Mary Rose
;
Farrugia, Mario
;
Scerri, Christian A.
2009-11
The significance of quantitative HB epidemiology in public health genomics and genetic models of complex disease
Felice, Alex
;
Galdies, Ruth
;
Cassar, Wilhelmina
;
Pizzuto, Monica
;
Borg, Joseph J.
;
Bugeja, Marisa
;
Caruana, Mary Rose
;
Farrugia, Mario
;
Scerri, Christian A.