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Cardiomyopathy in Coffin-Lowry syndrome.
Facher JJ, Regier EJ, Jacobs GH, Siwik E, Delaunoy JP, Robin NH. Facher JJ, et al. Among authors: robin nh. Am J Med Genet A. 2004 Jul 15;128A(2):176-8. doi: 10.1002/ajmg.a.30056. Am J Med Genet A. 2004. PMID: 15214012
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. 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
Sex-discordant monochorionic twins with blood and tissue chimerism.
Rodriguez-Buritica D, Rojnueangnit K, Messiaen LM, Mikhail FM, Robin NH. Rodriguez-Buritica D, et al. Among authors: robin nh. Am J Med Genet A. 2015 Apr;167A(4):872-7. doi: 10.1002/ajmg.a.37022. Epub 2015 Feb 23. Am J Med Genet A. 2015. PMID: 25708669
173 results