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P C Giordano

Showing results (41-50 of 72) with videos related to

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International Journal of Laboratory Hematology|June 3, 2009
Evaluating five dedicated automatic devices for haemoglobinopathy diagnostics in multi-ethnic populationsP Van Delft, E Lenters, M Bakker-Verweij, et al.
Journal of Medical Genetics|April 1, 1991
Homozygous beta+ thalassaemia owing to a mutation in the cleavage-polyadenylation sequence of the human beta globin geneM Losekoot, R Fodde, C L Harteveld, et al.
Hemoglobin|January 1, 1994
Hb Kurdistan [alpha 47(CE5)Asp-->Tyr], a new alpha chain variant in combination with beta (0)-thalassemiaP C Giordano, C L Harteveld, H Streng, et al.
Hemoglobin|March 11, 1998
Hb Godavari [alpha 95(G2)Pro-->Thr]: a neutral amino acid substitution in the alpha 1 beta 2 interface that modifies the electrophoretic mobility of hemoglobinH Wajcman, J Kister, J Riou, et al.
Journal of Medical Genetics|May 17, 2005
Nine unknown rearrangements in 16p13.3 and 11p15.4 causing alpha- and beta-thalassaemia characterised by high resolution multiplex ligation-dependent probe amplificationC L Harteveld, A Voskamp, M Phylipsen, et al.
European Journal of Biochemistry|October 15, 1996
Molecular characterization of ceratotoxin C, a novel antibacterial female-specific peptide of the ceratotoxin family from the medfly Ceratitis capitataM Rosetto, A G Manetti, P C Giordano, et al.
Annals of Human Genetics|January 1, 1991
Multiple recombination events are responsible for the heterogeneity of alpha(+)-thalassemia haplotypes among the forest tribes of Andhra Pradesh, IndiaR Fodde, C L Harteveld, M Losekoot, et al.
Nederlands Tijdschrift Voor Geneeskunde|August 5, 2006
[Acute anaemia in a Vietnamese patient with alpha-thalassaemia and a parvovirus infection]J Slomp, A Bosschaart, M Dousma, et al.
European Journal of Human Genetics : EJHG|April 10, 1999
A complex haemoglobinopathy diagnosis in a family with both beta zero- and alpha (zero/+)-thalassaemia homozygosityP C Giordano, C L Harteveld, L A Bok, et al.
Community Genetics|June 5, 2004
The molecular spectrum of beta-thalassemia and abnormal hemoglobins in the allochthonous and autochthonous dutch populationP C Giordano, C L Harteveld, A J Heister, et al.
Pageof 8

Showing results (41-50 of 72) with videos related to

Sort By:
Pageof 8
International Journal of Laboratory Hematology|June 3, 2009
Evaluating five dedicated automatic devices for haemoglobinopathy diagnostics in multi-ethnic populationsP Van Delft, E Lenters, M Bakker-Verweij, et al.
Journal of Medical Genetics|April 1, 1991
Homozygous beta+ thalassaemia owing to a mutation in the cleavage-polyadenylation sequence of the human beta globin geneM Losekoot, R Fodde, C L Harteveld, et al.
Hemoglobin|January 1, 1994
Hb Kurdistan [alpha 47(CE5)Asp-->Tyr], a new alpha chain variant in combination with beta (0)-thalassemiaP C Giordano, C L Harteveld, H Streng, et al.
Hemoglobin|March 11, 1998
Hb Godavari [alpha 95(G2)Pro-->Thr]: a neutral amino acid substitution in the alpha 1 beta 2 interface that modifies the electrophoretic mobility of hemoglobinH Wajcman, J Kister, J Riou, et al.
Journal of Medical Genetics|May 17, 2005
Nine unknown rearrangements in 16p13.3 and 11p15.4 causing alpha- and beta-thalassaemia characterised by high resolution multiplex ligation-dependent probe amplificationC L Harteveld, A Voskamp, M Phylipsen, et al.
European Journal of Biochemistry|October 15, 1996
Molecular characterization of ceratotoxin C, a novel antibacterial female-specific peptide of the ceratotoxin family from the medfly Ceratitis capitataM Rosetto, A G Manetti, P C Giordano, et al.
Annals of Human Genetics|January 1, 1991
Multiple recombination events are responsible for the heterogeneity of alpha(+)-thalassemia haplotypes among the forest tribes of Andhra Pradesh, IndiaR Fodde, C L Harteveld, M Losekoot, et al.
Nederlands Tijdschrift Voor Geneeskunde|August 5, 2006
[Acute anaemia in a Vietnamese patient with alpha-thalassaemia and a parvovirus infection]J Slomp, A Bosschaart, M Dousma, et al.
European Journal of Human Genetics : EJHG|April 10, 1999
A complex haemoglobinopathy diagnosis in a family with both beta zero- and alpha (zero/+)-thalassaemia homozygosityP C Giordano, C L Harteveld, L A Bok, et al.
Community Genetics|June 5, 2004
The molecular spectrum of beta-thalassemia and abnormal hemoglobins in the allochthonous and autochthonous dutch populationP C Giordano, C L Harteveld, A J Heister, et al.
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