Prenatal diagnosis of sickle hemoglobinopathies: The experience of the Columbia university comprehensive center for sickle cell disease

We report here an evaluation of 55 pregnancies at risk for a sickle hemoglobinopathy prenatally diagnosed by restriction-endonuclease analysis, with the endonucleases MstII and HpaI, of amniocyte DNA. The diagnosis was completed in all cases. Eleven fetuses were predicted to be affected, of which si...

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Detalhes bibliográficos
Main Authors: Driscoll, M. Catherine, Lerner, Norma, Anyane-Yeboa, Kwame, Maidman, Jack, Warburton, Dorothy, Schaefer-Rego, Kim, Hsu, Ruth, Ince, Carol, Malin, Joanne, Pallai, Michele, Mears, J. Gregory, Bank, Arthur
Formato: Artigo
Idioma:Inglês
Publicado em: 1987
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Original Articles
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC1684158/
https://ncbi.nlm.nih.gov/pubmed/3035920
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