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Page 1
Congenital lumbar hernia-A feature of diabetic embryopathy?
Stevens CA, Hogue JS, Hopkin RJ, Lombardo RC, Schrier Vergano SA. Stevens CA, et al. Am J Med Genet A. 2018 Nov;176(11):2243-2249. doi: 10.1002/ajmg.a.40381. Epub 2018 Oct 1. Am J Med Genet A. 2018. PMID: 30276953
Significance of bifid epiglottis.
Stevens CA, Ledbetter JC. Stevens CA, et al. Am J Med Genet A. 2005 May 1;134(4):447-9. doi: 10.1002/ajmg.a.30659. Am J Med Genet A. 2005. PMID: 15782417 Review.
Polymicrogyria and deletion 22q11.2 syndrome: window to the etiology of a common cortical malformation.
Robin NH, Taylor CJ, McDonald-McGinn DM, Zackai EH, Bingham P, Collins KJ, Earl D, Gill D, Granata T, Guerrini R, Katz N, Kimonis V, Lin JP, Lynch DR, Mohammed SN, Massey RF, McDonald M, Rogers RC, Splitt M, Stevens CA, Tischkowitz MD, Stoodley N, Leventer RJ, Pilz DT, Dobyns WB. Robin NH, et al. Among authors: stevens ca. Am J Med Genet A. 2006 Nov 15;140(22):2416-25. doi: 10.1002/ajmg.a.31443. Am J Med Genet A. 2006. PMID: 17036343
The hair collar sign.
Stevens CA, Galen W. Stevens CA, et al. Am J Med Genet A. 2008 Feb 15;146A(4):484-7. doi: 10.1002/ajmg.a.32161. Am J Med Genet A. 2008. PMID: 18203150
Familial odontoid hypoplasia.
Stevens CA, Pearce RG, Burton EM. Stevens CA, et al. Am J Med Genet A. 2009 Jun;149A(6):1290-2. doi: 10.1002/ajmg.a.32860. Am J Med Genet A. 2009. PMID: 19449423
170 results