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More on breast cancer guidelines.
Nassar BA, Ludman MD, Costa MT, Welch JP, Butts CA, Love JR, Hogg H, Beis MJ. Nassar BA, et al. Among authors: beis mj. CMAJ. 1998 Jun 2;158(11):1429; author reply 1429-30. CMAJ. 1998. PMID: 9629100 Free PMC article. No abstract available.
The role of Frizzled-4 mutations in familial exudative vitreoretinopathy and Coats disease.
Robitaille JM, Zheng B, Wallace K, Beis MJ, Tatlidil C, Yang J, Sheidow TG, Siebert L, Levin AV, Lam WC, Arthur BW, Lyons CJ, Jaakkola E, Tsilou E, Williams CA, Weaver RG Jr, Shields CL, Guernsey DL. Robitaille JM, et al. Among authors: beis mj. Br J Ophthalmol. 2011 Apr;95(4):574-9. doi: 10.1136/bjo.2010.190116. Epub 2010 Nov 21. Br J Ophthalmol. 2011. PMID: 21097938
Evidence for Cholinergic Dysfunction in Autosomal Dominant Kufs Disease.
Jarrett P, Easton A, Rockwood K, Dyack S, McCollum A, Siu V, Mirsattari SM, Massot-Tarrús A, Beis MJ, D'Souza N, Darvesh S. Jarrett P, et al. Among authors: beis mj. Can J Neurol Sci. 2018 Mar;45(2):150-157. doi: 10.1017/cjn.2017.261. Can J Neurol Sci. 2018. PMID: 29506599
Multilocus linkage identifies two new loci for a mendelian form of stroke, cerebral cavernous malformation, at 7p15-13 and 3q25.2-27.
Craig HD, Günel M, Cepeda O, Johnson EW, Ptacek L, Steinberg GK, Ogilvy CS, Berg MJ, Crawford SC, Scott RM, Steichen-Gersdorf E, Sabroe R, Kennedy CT, Mettler G, Beis MJ, Fryer A, Awad IA, Lifton RP. Craig HD, et al. Among authors: beis mj. Hum Mol Genet. 1998 Nov;7(12):1851-8. doi: 10.1093/hmg/7.12.1851. Hum Mol Genet. 1998. PMID: 9811928
[Moebius' syndrome associated with atrophic myopathy].
Neimann N, Pierson M, Rachmut H, Beis MJ, Brichet M. Neimann N, et al. Among authors: beis mj. Ann Med Nancy. 1965 Dec;4:1084-92. Ann Med Nancy. 1965. PMID: 5851828 French. No abstract available.
11 results