Restriction enzymes analysis of the DNA from two unrelated Italian families with Hb Hasharon, a variant Hb (alpha 47asp replaced by his) frequently occurring in the Polesine area in Italy, indicates that this variant is associated to an alpha globin gene deletion. The alpha Hash genotype most likely results from a mutation on an alpha thal2 genotyp
We describe a novel deletion form of alpha-thalassemia which removes a region of 31 kilobase encompa...
Hb O-Arab [beta 121(GH4)Glu-->Lys] was detected in two Mediterranean families, one from Southern Ita...
Hb City of Hope [β69(E13)GLSER] was detected by reversed phase high performance liquid chromatograph...
In subjects carrying the haemoglobin Hasharon mutation (alpha 47 replaced by His), originally from t...
We report the case of an Italian infant girl hand, in the Askenazy carriers of Hb Ha-from Polesine (...
Seven unrelated patients with hemoglobin (Hb) H disease and 27 individuals with alpha-chain structur...
Seven unrelated patients with hemoglobin (Hb) H disease and 27 individuals with alpha-chain structur...
Determination of HbA1c values with high performance liquid chromatography (HPLC) occasionally reveal...
Hb Hasharon has an electrophoretic mobility similar to that of Hb S in cellulose acetate and a mobil...
ABSTRACT. Hb Hasharon has an electrophoretic mobility similar to that of Hb S in cellulose acetate a...
This report is concerned with the evaluation of hematological parameters and of both relative (%) an...
We describe a new deletional form of alpha thalassaemia which encompasses the entire alpha-like glob...
Hemoglobin J Sardegna [alpha50(CD8)His-->Asn -->Asp] is a human Hb variant in which a posttranslatio...
Brazil has a multiethnic population with a high diversity of hemoglobinopathies. While screenings fo...
WOS: A1992HM87600017PubMed ID: 1581238We have analysed the alpha-globin gene defects present in seve...
We describe a novel deletion form of alpha-thalassemia which removes a region of 31 kilobase encompa...
Hb O-Arab [beta 121(GH4)Glu-->Lys] was detected in two Mediterranean families, one from Southern Ita...
Hb City of Hope [β69(E13)GLSER] was detected by reversed phase high performance liquid chromatograph...
In subjects carrying the haemoglobin Hasharon mutation (alpha 47 replaced by His), originally from t...
We report the case of an Italian infant girl hand, in the Askenazy carriers of Hb Ha-from Polesine (...
Seven unrelated patients with hemoglobin (Hb) H disease and 27 individuals with alpha-chain structur...
Seven unrelated patients with hemoglobin (Hb) H disease and 27 individuals with alpha-chain structur...
Determination of HbA1c values with high performance liquid chromatography (HPLC) occasionally reveal...
Hb Hasharon has an electrophoretic mobility similar to that of Hb S in cellulose acetate and a mobil...
ABSTRACT. Hb Hasharon has an electrophoretic mobility similar to that of Hb S in cellulose acetate a...
This report is concerned with the evaluation of hematological parameters and of both relative (%) an...
We describe a new deletional form of alpha thalassaemia which encompasses the entire alpha-like glob...
Hemoglobin J Sardegna [alpha50(CD8)His-->Asn -->Asp] is a human Hb variant in which a posttranslatio...
Brazil has a multiethnic population with a high diversity of hemoglobinopathies. While screenings fo...
WOS: A1992HM87600017PubMed ID: 1581238We have analysed the alpha-globin gene defects present in seve...
We describe a novel deletion form of alpha-thalassemia which removes a region of 31 kilobase encompa...
Hb O-Arab [beta 121(GH4)Glu-->Lys] was detected in two Mediterranean families, one from Southern Ita...
Hb City of Hope [β69(E13)GLSER] was detected by reversed phase high performance liquid chromatograph...