1,721,075 research outputs found
Le Basi biochimiche e molecolari delle talassemie e la diagnosi dell'Alfa-talassemia eterozigote
Recent aspects of molecular and biochemical basis of thalassemic syndromes are described together with laboratory methods suitable for diagnosis and screening of heterozygous α-thalassemia
Le Sindromi talassemiche
Recent developements of molecular biology and genetic of
thalassemia syndromes are discussed with special regard to
Sardinian situation. In the island heterozygous α and β thalassernias are present with incidences of 13,5 and 12,5% respectively.β+and δβ thalassemias together with several types of HPFH,
are also present.Screening programs at level of couples are suggested for the
prevention of β thalassemic homozygosity
High performance liquid chromatography of globin chains in the identification of human globin gene abnormalities.
84. Hadjisterkotis E., Masala B.: Vertebrate extinction in Mediterranean islets: an example from Cyprus.
Separation of globin chains by the reversed-phase high-performance liquid chromatography
Identification of Hb J-Sardegna [alpha50(CE8)His->Asp] by HPLC and its incidence in Northern Sardinia. Hemoglobin, 13:33-44, 1989.
A simple approach to the determination of the gamma chain composition of Hb F in adult human samples.
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