Selected Publications
Stewart DR, Huang A, Faravelli F, Anderlid BM, Medne L, Russell K, Kaur M, Rossi E, Tenconi R, Nordenskjold M, Gripp KW, Nicholson L, Meschino WS, Capua E, Quarrell OWJ, Flint J, Irons M, Giampietro PF, Scholwalter DB, Zaleski CA, Malacarne M, Zackai EH, Spinner NB, Krantz ID: Subtelomeric deletions of chromosome 9q: A novel microdeletion syndrome. Am. J. Med. Genet. Page: In press, 2004.
Kamath BM, Spinner NB, Emerick KM, Booth C, Chudley AE, Bason L, Piccoli DA, Krantz ID: Vacular Anomalies and Jagged1 Mutations. Circulation 109: 1354-1358, 2004.
Kamath BM, Krantz ID: Alagille Syndrome. Management of Genetic Syndromes. Allanson J, Cassidy S (eds.). John Wiley & Sons, Inc. Page: In press, 2004.
Krantz ID and Spinner NB: Notch Ligands: Jagged1 and Alagille Syndrome. Molecular Basis of Inborn Errors of Development. Epstein CJ, Erickson RP, Wynshaw-Boris A (eds.). McGraw-Hill, Page: 461-469, 2004.
Kamath BM, Krantz ID: Reply to correspondence from Kosztolanyi and Mehes "Supernumerary digital flexion creases" Am. J. Med. Genet. 121A: A:92, 2003.
Kamath BM, Loomes KM, Piccoli DA, Emerick KEM, Oakey RJ, Spinner NB, Krantz ID: Reply to correspondence from Sokol. Am. J. Med. Genet. Page: Online, 2003.
Kamath BM, Bason L, Piccoli DA, Krantz ID, Spinner NB: Consequences of JAG1 mutations. J. Med. Genet. 40: 891-895, 2003.
Bason LB, Spinner NB, Krantz ID: Alagille Syndrome. GeneClinicas:Medical Genetics Knowledge Base. University of Washington, Seattle, Page: Online, 2003.
Huang A, Stewart DR, Faravelli F, Anderlid BM, Kaur M, Rossi E, Gripp KW, Meschino WS, Quarrell PWJ, Irons M, Zaleski CA, Zackai EH, Budarf M, Spinner NB, Krantz ID: The 9q subtelomemeric microdeletion syndrome; Evidence for a gemonic susceptibility. Am. J. Hum. Genet. 73: 426, 2003.
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Last updated: 04/30/2009
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