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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: harrison s. 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.
Genetic basis of prune belly syndrome: screening for HNF1β gene.
Granberg CF, Harrison SM, Dajusta D, Zhang S, Hajarnis S, Igarashi P, Baker LA. Granberg CF, et al. Among authors: harrison sm. J Urol. 2012 Jan;187(1):272-8. doi: 10.1016/j.juro.2011.09.036. Epub 2011 Nov 23. J Urol. 2012. PMID: 22114815 Free PMC article.
Copy number variations in a population with prune belly syndrome.
Iqbal NS, Jascur TA, Harrison S, Chen C, Arevalo MK, Wong D, Sanchez E, Grimsby G, Wilson K, Baker LA. Iqbal NS, et al. Among authors: harrison s. Am J Med Genet A. 2018 Nov;176(11):2276-2283. doi: 10.1002/ajmg.a.40476. Epub 2018 Oct 4. Am J Med Genet A. 2018. PMID: 30285310 Free PMC article.
SCGN deficiency results in colitis susceptibility.
Sifuentes-Dominguez LF, Li H, Llano E, Liu Z, Singla A, Patel AS, Kathania M, Khoury A, Norris N, Rios JJ, Starokadomskyy P, Park JY, Gopal P, Liu Q, Tan S, Chan L, Ross T, Harrison S, Venuprasad K, Baker LA, Jia D, Burstein E. Sifuentes-Dominguez LF, et al. Among authors: harrison s. Elife. 2019 Oct 30;8:e49910. doi: 10.7554/eLife.49910. Elife. 2019. PMID: 31663849 Free PMC article.
3,487 results