Chromosomes, human, pair 9/geneticsRefine your research by the most used items
Author / Editor
- Antonarakis, Stylianos (1)
- Baban, Anwar (1)
- Bedeschi, Maria F. (1)
- Bengala, Mario (1)
- Bocciardi, Renata (1)
- Bouras, Constantin (1)
- Cerone, Roberto (1)
- Colussi, Gianluca (1)
- Di Duca, Marco (1)
- Divizia, Maria T. (1)
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remove all| Title | Authors / Editors | Date | |
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A spectrum of LMX1B mutations in Nail-Patella syndrome: new point mutations, deletion, and evidence of mosaicism in unaffected parents | Marini, Monica; Bocciardi, Renata; Gimelli, Stefania; Di Duca, Marco; ... Ravazzolo, Roberto | 2010 |
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Fluorescence in situ hybridization as a tool to characterize genetic alterations in pancreatic adenocarcinoma | Genevay-Infante, Muriel; Dumonceau, Jean-Marc; Pepey, Beatrice; Pache, Jean-Claude; ... Mckee, Thomas Alexander | 2010 |
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Tau and neurofilaments in a family with frontotemporal dementia unlinked to chromosome 17q21-22 | Savioz, Armand; Riederer, Beat M; Heutink, Peter; Rizzu, Patrizia; ... Leuba, Geneviève | 2003 |
