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978 results

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Results are displayed in a computed author sort order. The Publication Date timeline is not available.
Page 1
Spectrum of clinical features associated with interstitial chromosome 22q11 deletions: a European collaborative study.
Ryan AK, Goodship JA, Wilson DI, Philip N, Levy A, Seidel H, Schuffenhauer S, Oechsler H, Belohradsky B, Prieur M, Aurias A, Raymond FL, Clayton-Smith J, Hatchwell E, McKeown C, Beemer FA, Dallapiccola B, Novelli G, Hurst JA, Ignatius J, Green AJ, Winter RM, Brueton L, Brøndum-Nielsen K, Scambler PJ, et al. Ryan AK, et al. Among authors: dallapiccola b. J Med Genet. 1997 Oct;34(10):798-804. doi: 10.1136/jmg.34.10.798. J Med Genet. 1997. PMID: 9350810 Free PMC article.
How many breaks do we need to CATCH on 22q11?
Dallapiccola B, Pizzuti A, Novelli G. Dallapiccola B, et al. Am J Hum Genet. 1996 Jul;59(1):7-11. Am J Hum Genet. 1996. PMID: 8659546 Free PMC article. Review. No abstract available.
Tricuspid atresia and 22q11 deletion.
Marino B, Digilio MC, Novelli G, Giannotti A, Dallapiccola B. Marino B, et al. Among authors: dallapiccola b. Am J Med Genet. 1997 Oct 3;72(1):40-2. doi: 10.1002/(sici)1096-8628(19971003)72:1<40::aid-ajmg8>3.0.co;2-z. Am J Med Genet. 1997. PMID: 9295072
Mutations in a new gene in Ellis-van Creveld syndrome and Weyers acrodental dysostosis.
Ruiz-Perez VL, Ide SE, Strom TM, Lorenz B, Wilson D, Woods K, King L, Francomano C, Freisinger P, Spranger S, Marino B, Dallapiccola B, Wright M, Meitinger T, Polymeropoulos MH, Goodship J. Ruiz-Perez VL, et al. Among authors: dallapiccola b. Nat Genet. 2000 Mar;24(3):283-6. doi: 10.1038/73508. Nat Genet. 2000. PMID: 10700184
Meiotic drive at the myotonic dystrophy locus.
Gennarelli M, Dallapiccola B, Baiget M, Martorell L, Novelli G. Gennarelli M, et al. Among authors: dallapiccola b. J Med Genet. 1994 Dec;31(12):980. doi: 10.1136/jmg.31.12.980. J Med Genet. 1994. PMID: 7891386 Free PMC article. No abstract available.
Mutations of UFD1L are not responsible for the majority of cases of DiGeorge Syndrome/velocardiofacial syndrome without deletions within chromosome 22q11.
Wadey R, McKie J, Papapetrou C, Sutherland H, Lohman F, Osinga J, Frohn I, Hofstra R, Meijers C, Amati F, Conti E, Pizzuti A, Dallapiccola B, Novelli G, Scambler P. Wadey R, et al. Among authors: dallapiccola b. Am J Hum Genet. 1999 Jul;65(1):247-9. doi: 10.1086/302468. Am J Hum Genet. 1999. PMID: 10364538 Free PMC article. No abstract available.
978 results