3 results for author:"Pallotta R." in Literature citations
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| Loss of the BMP antagonist, SMOC-1, causes Ophthalmo-acromelic (Waardenburg Anophthalmia) syndrome in humans and mice. Rainger J., van Beusekom E., Ramsay J.K., McKie L., Al-Gazali L., Pallotta R., Saponari A., Branney P., Fisher M., Morrison H. et al. PLoS Genet. 7:e1002114-e1002114(2011) · Mapped (4) |
| Mandibuloacral dysplasia is caused by a mutation in LMNA-encoding lamin A/C. Novelli G., Muchir A., Sangiuolo F., Helbling-Leclerc A., D'Apice M.R., Massart C., Capon F., Sbraccia P., Federici M., Lauro R. et al. Am. J. Hum. Genet. 71:426-431(2002) · UniProtKB (1) · Mapped (7) |
| A patient defines the interstitial 1q deletion syndrome characterized by antithrombin III deficiency. Pallotta R., Dalpra L., Miozzo M., Ehresmann T., Fusilli P. Am. J. Med. Genet. 104:282-286(2001) · Mapped (10) |