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Page 1
Autosomal dominant transmission of familial laterality defects.
Casey B, Cuneo BF, Vitali C, van Hecke H, Barrish J, Hicks J, Ballabio A, Hoo JJ. Casey B, et al. Among authors: cuneo bf. Am J Med Genet. 1996 Feb 2;61(4):325-8. doi: 10.1002/(SICI)1096-8628(19960202)61:4<325::AID-AJMG5>3.0.CO;2-T. Am J Med Genet. 1996. PMID: 8834043
Frequency of 22q11 deletions in patients with conotruncal defects.
Goldmuntz E, Clark BJ, Mitchell LE, Jawad AF, Cuneo BF, Reed L, McDonald-McGinn D, Chien P, Feuer J, Zackai EH, Emanuel BS, Driscoll DA. Goldmuntz E, et al. Among authors: cuneo bf. J Am Coll Cardiol. 1998 Aug;32(2):492-8. doi: 10.1016/s0735-1097(98)00259-9. J Am Coll Cardiol. 1998. PMID: 9708481 Free article.
Substantiation of trophoblast transport of maternal anti-SSA/Ro autoantibodies in fetuses with rapidly progressive cardiac injury: implications for neonatal Fc receptor blockade.
Buyon JP, Carlucci PM, Cuneo BF, Masson M, Izmirly P, Sachan N, Brandt JS, Mehta-Lee S, Halushka M, Thomas K, Fox M, Phoon CK, Ludomirsky A, Srinivasan R, Lam G, Wainwright BJ, Fraser N, Clancy R. Buyon JP, et al. Among authors: cuneo bf. Lancet Rheumatol. 2024 Nov 15:S2665-9913(24)00331-X. doi: 10.1016/S2665-9913(24)00331-X. Online ahead of print. Lancet Rheumatol. 2024. PMID: 39557050 No abstract available.
98 results