Browsing by Subject Genetic disorders

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Issue DateTitleAuthor(s)
1969Abnormalities of hemoglobin A₂Vella, Francis
1980Adult and fetal hemoglobin production in erythroid colonies from subjects with β-thalassemia or with hereditary persistence of fetal hemoglobin (HPFH)Huisman, Titus Hendrik Jan; Reese, A. L.; Gravely, Marsha E.; Wilson, Jerry B.; Webber, Brooke B.; Felice, Alex E.
1973Albinism : a case reportPsaila, Angelo J.
2015Autosomal dominant polycystic kidney diseaseAttard, Stephanie
1976A case of Goldenhar syndrome associated with an inguinal hernia and extensive renal, uretric, and bladder abnormalitiesDamato, Francis Joseph
2002Confidentiality, privacy and genetic testingCuschieri, Alfred
1997Congenital heart disease in MaltaGrech, Victor E.
2010-12Epigenetics and its medical repercussionsGrech, Alfred; Baldacchino, Sandra; Tufignio, Marcel
1992Exploration of the genetic basis of coagulation factor VII deficiency in a Maltese familyShinawi, Connie
2015Free our genes : a liberal reliefEllul, Ian C.
2010Genetic screening of heredity diseasesGamudi, Donia; Blundell, Renald
1970Hereditary diaphorase deficiency methemoglobinemia in Maltese familiesVassallo, Luis A.; Cauchi, Maurice N.
2013HERVs, transposons and human diseases : part 3Grech, Alfred; Baldacchino, Sandra
2012HERVs, transposons and human diseases : part IGrech, Alfred; Baldacchino, Sandra
2013HERVs, transposons and human diseases : part IIGrech, Alfred; Baldacchino, Sandra
2010Inherited cancer syndromesGamudi, Donia; Blundell, Renald
2017An introduction to epigeneticsBarbara, Maria Andria; Abdilla, Ylenia; Calleja-Agius, Jean
2008Molecular SNPlotypes™ with common alleles reflects expression profile in Diabetes Mellitus Type 2Al-Ashtar, Ali Ahmed
1995New insight into genetic disease : the role of trinucleotide repeat expansionsCuschieri, Alfred
2010Nurses' perceptions about alternative residential facilities for Huntington's disease patients : a qualitative studyCassar, Rebecca (2010)