Rastreio Neonatal de Hemoglobinopatias numa População Residente em Portugal

Autor: Peres, MJ, Carreiro, MH, Machado, MC, Seixas, T, Picanço, I, Batalha, L, Lavinha, J, Martins, MC

Publikováno v: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Agência para a Sociedade do Conhecimento (UMIC)-FCT-Sociedade da Informação
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The primary objective of newborn screening of hemoglobinopathies is the early identification of infants with sickle cell disease, as they are at increased clinical risk. Other goals include the identification of other types of clinically significant

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https://hdl.handle.net/10400.17/633

POLYMORPHISM AND MOLECULAR PATHOLOGY OF THE ALPHA-GLOBIN GENE-CLUSTER (16P13.3-PTER) IN THE PORTUGUESE POPULATION

Autor: Peres, Mj, Picanco, I., Almeida, S., Romao, L., Morais, S., Carreiro, Mh, Martins, Mc, Lavinha, J.

Publikováno v: ResearcherID
CIÊNCIAVITAE

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http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=ORCID&SrcApp=OrcidOrg&DestLinkType=FullRecord&DestApp=WOS_CPL&KeyUT=WOS:A1992JK23000024&KeyUID=WOS:A1992JK23000024

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[Neonatal screening of hemoglobinopathies in a population residing in Portugal].

Autor: Peres MJ; Departamento de Genética e Biologia Médica, Instituto Nacìonal de Saúde Dr Ricardo Jorge, Alfredo da Costa, Lisboa., Carreiro MH, Machado MC, Seixas T, Picanço I, Batalha L, Lavinha J, Martins MC

Publikováno v: Acta medica portuguesa [Acta Med Port] 1996 Apr-Jun; Vol. 9 (4-6), pp. 135-9.