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Clinical Chemistry and Laboratory Medicine|April 25, 2013
Prenatal diagnosis of cystic fibrosis: an experience of 181 casesRossella Tomaiuolo, Paola Nardiello, Pasquale Martinelli, et al.Clinical Chemistry and Laboratory Medicine|May 16, 2003
Haemophilia B: from molecular diagnosis to gene therapyGiuseppe Castaldo, Paola Nardiello, Fabiana Bellitti, et al.Clinical Chemistry and Laboratory Medicine|April 19, 2007
Haemophilia A: molecular insightsGiuseppe Castaldo, Valeria D'Argenio, Paola Nardiello, et al.Ophthalmology|October 1, 2011
Limbal stem cell deficiency and ocular phenotype in ectrodactyly-ectodermal dysplasia-clefting syndrome caused by p63 mutationsEnzo Di Iorio, Stephen B Kaye, Diego Ponzin, et al.American Journal of Medical Genetics. Part A|June 29, 2012
A novel de novo missense mutation in TP63 underlying germline mosaicism in AEC syndrome: implications for recurrence risk and prenatal diagnosisVanessa Barbaro, Paola Nardiello, Giuseppe Castaldo, et al.Pageof 1