The genetic defect in multiple endocrine neoplasia type 2A maps next to the centromere of chromosome 10

Multiple endocrine neoplasia type 2A (MEN2A) is a rare cancer syndrome that is inherited in an apparently autosomal dominant fashion. Previous linkage studies had assigned the MEN2A locus to chromosome 10 in the pericentromeric region. We recently have described several new easily scorable RFLPs for...

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Detalhes bibliográficos
Main Authors: Wu, Jingshi, Carson, Nancy L., Myers, Shirley, Pakstis, Andrew J., Kidd, Judith R., Castiglione, Carmela M., Anderson, Linda, Hoyle, L. Suzanne, Genel, Myron, Verdy, Maurice, Jackson, Charles E., Simpson, Nancy E., Kidd, Kenneth K.
Formato: Artigo
Idioma:Inglês
Publicado em: 1990
Assuntos:
Original Articles
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC1683638/
https://ncbi.nlm.nih.gov/pubmed/1968709
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