2 results for author:"Zinn A.B." in Literature citations
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| Delineation of the Marfan phenotype associated with mutations in exons 23-32 of the FBN1 gene. Putnam E.A., Cho M., Zinn A.B., Towbin J.A., Byers P.H., Milewicz D.M. Am. J. Med. Genet. 62:233-242(1996) · UniProtKB (1) · Mapped (8) |
| Variable expression of osteogenesis imperfecta in a nuclear family is explained by somatic mosaicism for a lethal point mutation in the alpha 1(I) gene (COL1A1) of type I collagen in a parent. Wallis G.A., Starman B.J., Zinn A.B., Byers P.H. Am. J. Hum. Genet. 46:1034-1040(1990) · UniProtKB (1) |