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Page 1
Holoprosencephaly in a family segregating novel variants in ZIC2 and GLI2.
Wannasilp N, Solomon BD, Warren-Mora N, Clegg NJ, Delgado MR, Lacbawan F, Hu P, Winder TL, Roessler E, Muenke M. Wannasilp N, et al. Among authors: warren mora n. Am J Med Genet A. 2011 Apr;155A(4):860-4. doi: 10.1002/ajmg.a.33903. Epub 2011 Mar 17. Am J Med Genet A. 2011. PMID: 21416594
Analysis of FOXF1 and the FOX gene cluster in patients with VACTERL association.
Agochukwu NB, Pineda-Alvarez DE, Keaton AA, Warren-Mora N, Raam MS, Kamat A, Chandrasekharappa SC, Solomon BD. Agochukwu NB, et al. Among authors: warren mora n. Eur J Med Genet. 2011 May-Jun;54(3):323-8. doi: 10.1016/j.ejmg.2011.01.007. Epub 2011 Feb 26. Eur J Med Genet. 2011. PMID: 21315191 Free PMC article.
Analysis of cardiac anomalies in VACTERL association.
Cunningham BK, Hadley DW, Hannoush H, Meltzer AC, Niforatos N, Pineda-Alvarez D, Sachdev V, Warren-Mora N, Solomon BD. Cunningham BK, et al. Among authors: warren mora n. Birth Defects Res A Clin Mol Teratol. 2013 Dec;97(12):792-7. doi: 10.1002/bdra.23211. Birth Defects Res A Clin Mol Teratol. 2013. PMID: 24343877 Free PMC article.
An approach to the identification of anomalies and etiologies in neonates with identified or suspected VACTERL (vertebral defects, anal atresia, tracheo-esophageal fistula with esophageal atresia, cardiac anomalies, renal anomalies, and limb anomalies) association.
Solomon BD, Baker LA, Bear KA, Cunningham BK, Giampietro PF, Hadigan C, Hadley DW, Harrison S, Levitt MA, Niforatos N, Paul SM, Raggio C, Reutter H, Warren-Mora N. Solomon BD, et al. Among authors: warren mora n. J Pediatr. 2014 Mar;164(3):451-7.e1. doi: 10.1016/j.jpeds.2013.10.086. Epub 2013 Dec 12. J Pediatr. 2014. PMID: 24332453 Free PMC article. Review. No abstract available.