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Genetic testing in couples undergoing assisted reproduction technique protocols.
Expert Opin Med Diagn. 2009 Sep;3(5):571-83. doi: 10.1517/17530050902970986. Epub 2009 Jul 29.
Expert Opin Med Diagn. 2009.
PMID: 23495986
Testis transcriptome analysis in male infertility: new insight on the pathogenesis of oligo-azoospermia in cases with and without AZFc microdeletion.
Gatta V, Raicu F, Ferlin A, Antonucci I, Scioletti AP, Garolla A, Palka G, Foresta C, Stuppia L.
Gatta V, et al. Among authors: scioletti ap.
BMC Genomics. 2010 Jun 24;11:401. doi: 10.1186/1471-2164-11-401.
BMC Genomics. 2010.
PMID: 20576090
Free PMC article.
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Two novel mutations affecting splicing in the IRF6 gene associated with van der Woude syndrome.
Scioletti AP, Brancati F, Gatta V, Antonucci I, Peissel B, Pizzuti A, Mortellaro C, Tetè S, Gherlone E, Palka G, Stuppia L.
Scioletti AP, et al.
J Craniofac Surg. 2010 Sep;21(5):1654-6. doi: 10.1097/SCS.0b013e3181ef69ef.
J Craniofac Surg. 2010.
PMID: 20856073
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High prevalence of BRCA1 deletions in BRCAPRO-positive patients with high carrier probability.
Veschi S, Aceto G, Scioletti AP, Gatta V, Palka G, Cama A, Mariani-Costantini R, Battista P, Calò V, Barbera F, Bazan V, Russo A, Stuppia L.
Veschi S, et al. Among authors: scioletti ap.
Ann Oncol. 2007 Jun;18 Suppl 6:vi86-92. doi: 10.1093/annonc/mdm233.
Ann Oncol. 2007.
PMID: 17591842
Free article.
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Microarray expression profiling of human dental pulp from single subject.
Tete S, Mastrangelo F, Scioletti AP, Tranasi M, Raicu F, Paolantonio M, Stuppia L, Vinci R, Gherlone E, Ciampoli C, Sberna MT, Conti P.
Tete S, et al. Among authors: scioletti ap.
Clin Invest Med. 2008;31(2):E55-61. doi: 10.25011/cim.v31i2.3364.
Clin Invest Med. 2008.
PMID: 18377761
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Dentin sialophosphoprotein expression during human matrix development.
Mastrangelo F, Scioletti AP, Tranasi M, Tecco S, Sberna MT, Vinci R, Grilli A, Stuppia L, Gherlone E, Tete S.
Mastrangelo F, et al. Among authors: scioletti ap.
J Biol Regul Homeost Agents. 2007;21(1-2):33-9.
J Biol Regul Homeost Agents. 2007.
PMID: 18211748
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Germline BRAF mutations in Noonan, LEOPARD, and cardiofaciocutaneous syndromes: molecular diversity and associated phenotypic spectrum.
Sarkozy A, Carta C, Moretti S, Zampino G, Digilio MC, Pantaleoni F, Scioletti AP, Esposito G, Cordeddu V, Lepri F, Petrangeli V, Dentici ML, Mancini GM, Selicorni A, Rossi C, Mazzanti L, Marino B, Ferrero GB, Silengo MC, Memo L, Stanzial F, Faravelli F, Stuppia L, Puxeddu E, Gelb BD, Dallapiccola B, Tartaglia M.
Sarkozy A, et al. Among authors: scioletti ap.
Hum Mutat. 2009 Apr;30(4):695-702. doi: 10.1002/humu.20955.
Hum Mutat. 2009.
PMID: 19206169
Free PMC article.
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