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Search Results - Principi, Cintia
Search Results - Principi, Cintia
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D−− phenotype caused by a novel RHCE null allele
by
Principi, Cintia
,
Trucco Boggione, Carolina
,
Ensinck, Alejandra
,
Posner, Victoria
,
Luján Brajovich, Melina
,
Stettler, Silvina
,
Mattaloni, Stella
,
Biondi, Claudia
,
Cotorruelo, Carlos
Published in
Transfusion (Philadelphia, Pa.)
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A novel SNV on a previously reported hybrid RHCE background is responsible for an Rh haplotype potentially involved in the generation of an Rh null phenotype
by
Principi, Cintia
,
Trucco Boggione, Carolina
,
Mestra Campo, Bleidy
,
Posner, Victoria
,
Zani, Nestor
,
Luján Brajovich, Melina
,
Villanueva, Mariana
,
Mattaloni, Stella Maris
,
Ensinck, Alejandra
,
Biondi, Claudia
,
Cotorruelo, Carlos
Published in
Transfusion (Philadelphia, Pa.)
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Extensive clinical, serologic and molecular studies lead to the first reported Rh mod phenotype in Argentina
by
Mufarrege, Nicolás
,
Franco, Noelia
,
Trucco Boggione, Carolina
,
Arnoni, Carine
,
de PaulaVendrame, Tatiane
,
Bartoli, Sonia
,
Ensinck, Alejandra
,
Principi, Cintia
,
Lujan Brajovich, Melina
,
Mattaloni, Stella
,
Riquelme, Bibiana
,
Biondi, Claudia
,
Castilho, Lilian
,
Cotorruelo, Carlos
Published in
Transfusion (Philadelphia, Pa.)
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Extensive clinical, serologic and molecular studies lead to the first reported Rhmod phenotype in Argentina
by
Mufarrege, Nicolás
,
Franco, Noelia
,
Trucco Boggione, Carolina
,
Arnoni, Carine
,
Paula Vendrame, Tatiane
,
Bartoli, Sonia
,
Ensinck, Alejandra
,
Principi, Cintia
,
Lujan Brajovich, Melina
,
Mattaloni, Stella
,
Riquelme, Bibiana
,
Biondi, Claudia
,
Castilho, Lilian
,
Cotorruelo, Carlos
Published in
Transfusion (Philadelphia, Pa.)
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The novel RHD c. 325A >G single nucleotide variation found in Argentineans leads to a partial D phenotype
by
Mufarrege, Nicolás
,
Trucco Boggione, Carolina
,
Puppo, Mónica
,
Ensinck, Alejandra
,
Príncipi, Cintia
,
Brajovich, Melina Luján
,
Mattaloni, Stella
,
Biondi, Claudia
,
Kuperman, Silvina
,
Cotorruelo, Carlos
Published in
Transfusion (Philadelphia, Pa.)
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The novel RHD c.325A>G single nucleotide variation found in Argentineans leads to a partial D phenotype
by
Mufarrege, Nicolás
,
Trucco Boggione, Carolina
,
Puppo, Mónica
,
Ensinck, Alejandra
,
Príncipi, Cintia
,
Brajovich, Melina Luján
,
Mattaloni, Stella
,
Biondi, Claudia
,
Kuperman, Silvina
,
Cotorruelo, Carlos
Published in
Transfusion (Philadelphia, Pa.)
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