Zobrazeno 1 - 2
of 2
pro vyhledávání: '"L S, Hoyle"'
Autor:
J S, Wu, N L, Carson, S, Myers, A J, Pakstis, J R, Kidd, C M, Castiglione, L, Anderson, L S, Hoyle, M, Genel, M, Verdy
Publikováno v:
American journal of human genetics. 46(3)
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 ha
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::193e16cc31a5b725b4f2e4bbae6225a5
https://pubmed.ncbi.nlm.nih.gov/1968709
https://pubmed.ncbi.nlm.nih.gov/1968709
Autor:
L. Anderson, P.J. Goodfellow, Jingshi Wu, N. L. Carson, Shirley M. Myers, Kenneth K. Kidd, N. E. Simpson, L. Giuffra, L. S. Hoyle
Publikováno v:
Human Genetics. 83:383-390
The beta subunit of the human fibronectin receptor (FNRB) is a transmembrane protein belonging to the VLA (very late antigens of activation) family. Using pGEM-32, a 2.5-kb partial cDNA clone corresponding to the 3' portion of the human FNRB locus, m
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::091452ccac4a80d29db01577b7a44b5f
https://doi.org/10.1007/bf00291386
https://doi.org/10.1007/bf00291386