Výsledky vyhledávání - "M H C, Ferraz"

Homozygous Hb Stanleyville-II [alpha2 78(EF7) Asn>Lys; HBA2:c.237C>A, not C>G] associated with genotype −α3.7/−α3.7 in two Brazilian families

Autor: Fernanda Silva Pimentel, M. H. C. Ferraz, José Nélio Januário, D. Méndez del Castillo, Marcilene Rezende Silva, Marcos Borato Viana, Carlos Perone, Nara de Oliveira Carvalho

Publikováno v: International Journal of Laboratory Hematology. 33:566-569

Summary Introduction: Several hemoglobin variants have electrophoretic behavior similar to hemoglobin S, which may lead to false diagnosis for sickle-cell disorders in newborn screening programs. A homozygous hemoglobin with S mobility was detected i

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::386098b25095778bfee48a9acc8c8a0e
https://doi.org/10.1111/j.1751-553x.2011.01321.x

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Homozygous Hb Stanleyville-II [alpha2 78(EF7) AsnLys; HBA2:c.237CA, not CG] associated with genotype -α 3.7/-α 3.7 in two Brazilian families

Autor: F S, Pimentel, M R, Silva, M H C, Ferraz, N O, Carvalho, C, Perone, D Méndez, del Castillo, J N, Januario, M B, Viana

Publikováno v: International journal of laboratory hematology. 33(6)

Several hemoglobin variants have electrophoretic behavior similar to hemoglobin S, which may lead to false diagnosis for sickle-cell disorders in newborn screening programs. A homozygous hemoglobin with S mobility was detected in two unrelated babies

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::5757d80af759ad4171e5f7074edb95f0
https://pubmed.ncbi.nlm.nih.gov/21470372

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