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D Gasperini

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Genetic Counseling (Geneva, Switzerland)|April 16, 2004
Duplication of the terminal band of the long arm of chromosome 7: a new caseL Boccone, D Gasperini, G Pilloni, et al.
Hemoglobin|November 1, 1994
Hb A2-Sant' Antioco [alpha 2 delta (2)93(F9)Cys-->Gly]: a new delta chain variant identified by sequencing of amplified DNAR Galanello, D Gasperini, L Perseu, et al.
Human Mutation|January 1, 1994
A novel delta O-thalassemia mutation: TGG-->TAG (TRP-->STOP) at codon 37D Gasperini, L Perseu, P Cossu, et al.
Blood|April 1, 1993
The repeated sequence (AT)x(T)y upstream to the beta-globin gene is a simple polymorphismR Galanello, A Meloni, D Gasperini, et al.
Nature|December 29, 2000
Evidence from Sardinian basalt geochemistry for recycling of plume heads into the Earth's mantleD Gasperini, J Blichert-Toft, D Bosch, et al.
Haematologica|September 1, 1992
Hemoglobin Sabine [beta 91 (F7) Leu-->Pro]: occurrence in a Sardinian individual with hemolytic anemia and inclusion bodiesD Gasperini, R Galanello, M A Melis, et al.
British Journal of Haematology|May 1, 1993
Normal individuals with high Hb A2 levelsD Gasperini, A Cao, L Paderi, et al.
British Journal of Haematology|June 1, 1995
A promoter mutation, C-->T at position -92, leading to silent beta-thalassaemiaM C Rosatelli, V Faà, A Meloni, et al.
American Journal of Hematology|January 10, 1998
Heterozygous beta-thalassemia with thalassemia intermedia phenotypeD Gasperini, L Perseu, M A Melis, et al.
American Journal of Hematology|January 1, 1992
Heterozygous beta-thalassemia: relationship between the hematological phenotype and the type of beta-thalassemia mutationC Rosatelli, G B Leoni, T Tuveri, et al.
Pageof 2

Showing results (1-10 of 14) with videos related to

Sort By:
Pageof 2
Genetic Counseling (Geneva, Switzerland)|April 16, 2004
Duplication of the terminal band of the long arm of chromosome 7: a new caseL Boccone, D Gasperini, G Pilloni, et al.
Hemoglobin|November 1, 1994
Hb A2-Sant' Antioco [alpha 2 delta (2)93(F9)Cys-->Gly]: a new delta chain variant identified by sequencing of amplified DNAR Galanello, D Gasperini, L Perseu, et al.
Human Mutation|January 1, 1994
A novel delta O-thalassemia mutation: TGG-->TAG (TRP-->STOP) at codon 37D Gasperini, L Perseu, P Cossu, et al.
Blood|April 1, 1993
The repeated sequence (AT)x(T)y upstream to the beta-globin gene is a simple polymorphismR Galanello, A Meloni, D Gasperini, et al.
Nature|December 29, 2000
Evidence from Sardinian basalt geochemistry for recycling of plume heads into the Earth's mantleD Gasperini, J Blichert-Toft, D Bosch, et al.
Haematologica|September 1, 1992
Hemoglobin Sabine [beta 91 (F7) Leu-->Pro]: occurrence in a Sardinian individual with hemolytic anemia and inclusion bodiesD Gasperini, R Galanello, M A Melis, et al.
British Journal of Haematology|May 1, 1993
Normal individuals with high Hb A2 levelsD Gasperini, A Cao, L Paderi, et al.
British Journal of Haematology|June 1, 1995
A promoter mutation, C-->T at position -92, leading to silent beta-thalassaemiaM C Rosatelli, V Faà, A Meloni, et al.
American Journal of Hematology|January 10, 1998
Heterozygous beta-thalassemia with thalassemia intermedia phenotypeD Gasperini, L Perseu, M A Melis, et al.
American Journal of Hematology|January 1, 1992
Heterozygous beta-thalassemia: relationship between the hematological phenotype and the type of beta-thalassemia mutationC Rosatelli, G B Leoni, T Tuveri, et al.
Pageof 2