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Year Number of Results
1999 3
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Page 1
Clinical and molecular genetics of Alagille syndrome.
Krantz ID, Piccoli DA, Spinner NB. Krantz ID, et al. Curr Opin Pediatr. 1999 Dec;11(6):558-64. doi: 10.1097/00008480-199912000-00015. Curr Opin Pediatr. 1999. PMID: 10590916 Review.
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 and the Jagged1 gene.
Piccoli DA, Spinner NB. Piccoli DA, et al. Semin Liver Dis. 2001 Nov;21(4):525-34. doi: 10.1055/s-2001-19036. Semin Liver Dis. 2001. PMID: 11745040 Review.
Craniosynostosis in Alagille syndrome.
Kamath BM, Stolle C, Bason L, Colliton RP, Piccoli DA, Spinner NB, Krantz ID. Kamath BM, et al. Am J Med Genet. 2002 Oct 1;112(2):176-80. doi: 10.1002/ajmg.10608. Am J Med Genet. 2002. PMID: 12244552
Consequences of JAG1 mutations.
Kamath BM, Bason L, Piccoli DA, Krantz ID, Spinner NB. Kamath BM, et al. J Med Genet. 2003 Dec;40(12):891-5. doi: 10.1136/jmg.40.12.891. J Med Genet. 2003. PMID: 14684686 Free PMC article.
Subtelomeric deletions of chromosome 6p: molecular and cytogenetic characterization of three new cases with phenotypic overlap with Ritscher-Schinzel (3C) syndrome.
Descipio C, Schneider L, Young TL, Wasserman N, Yaeger D, Lu F, Wheeler PG, Williams MS, Bason L, Jukofsky L, Menon A, Geschwindt R, Chudley AE, Saraiva J, Schinzel AA, Guichet A, Dobyns WE, Toutain A, Spinner NB, Krantz ID. Descipio C, et al. Am J Med Genet A. 2005 Apr 1;134A(1):3-11. doi: 10.1002/ajmg.a.30573. Am J Med Genet A. 2005. PMID: 15704124 Review.
25 results