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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2009 1
2010 4
2011 3
2012 4
2013 1
2014 1
2015 5
2016 5
2017 1
2019 1
2020 1
2021 1
2024 0

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20 results

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Page 1
Notch signaling in human development and disease.
Penton AL, Leonard LD, Spinner NB. Penton AL, et al. Semin Cell Dev Biol. 2012 Jun;23(4):450-7. doi: 10.1016/j.semcdb.2012.01.010. Epub 2012 Jan 28. Semin Cell Dev Biol. 2012. PMID: 22306179 Free PMC article. Review.
Alagille syndrome: Genetics and Functional Models.
Gilbert MA, Spinner NB. Gilbert MA, et al. Curr Pathobiol Rep. 2017 Sep;5(3):233-241. doi: 10.1007/s40139-017-0144-8. Curr Pathobiol Rep. 2017. PMID: 29270332 Free PMC article.
NOTCH2 mutations in Alagille syndrome.
Kamath BM, Bauer RC, Loomes KM, Chao G, Gerfen J, Hutchinson A, Hardikar W, Hirschfield G, Jara P, Krantz ID, Lapunzina P, Leonard L, Ling S, Ng VL, Hoang PL, Piccoli DA, Spinner NB. Kamath BM, et al. J Med Genet. 2012 Feb;49(2):138-44. doi: 10.1136/jmedgenet-2011-100544. Epub 2011 Dec 29. J Med Genet. 2012. PMID: 22209762 Free PMC article.
Renal anomalies in Alagille syndrome: a disease-defining feature.
Kamath BM, Podkameni G, Hutchinson AL, Leonard LD, Gerfen J, Krantz ID, Piccoli DA, Spinner NB, Loomes KM, Meyers K. Kamath BM, et al. Am J Med Genet A. 2012 Jan;158A(1):85-9. doi: 10.1002/ajmg.a.34369. Epub 2011 Nov 21. Am J Med Genet A. 2012. PMID: 22105858 Free PMC article.
Clinical utility gene card for: Alagille Syndrome (ALGS).
Leonard LD, Chao G, Baker A, Loomes K, Spinner NB. Leonard LD, et al. Eur J Hum Genet. 2014 Mar;22(3). doi: 10.1038/ejhg.2013.140. Epub 2013 Jul 24. Eur J Hum Genet. 2014. PMID: 23881058 Free PMC article. No abstract available.
Pathologic lower extremity fractures in children with Alagille syndrome.
Bales CB, Kamath BM, Munoz PS, Nguyen A, Piccoli DA, Spinner NB, Horn D, Shults J, Leonard MB, Grimberg A, Loomes KM. Bales CB, et al. J Pediatr Gastroenterol Nutr. 2010 Jul;51(1):66-70. doi: 10.1097/MPG.0b013e3181cb9629. J Pediatr Gastroenterol Nutr. 2010. PMID: 20453673 Free PMC article.
Mosaic trisomy 17: variable clinical and cytogenetic presentation.
Daber R, Chapman KA, Ruchelli E, Kasperski S, Mulchandani S, Thiel BD, Hakonarson H, Zackai EH, Conlin LK, Spinner NB. Daber R, et al. Am J Med Genet A. 2011 Oct;155A(10):2489-95. doi: 10.1002/ajmg.a.34172. Am J Med Genet A. 2011. PMID: 21998853 Free PMC article.
20 results