Margherita Silengo
Clinical Genetics
Department of Paediatrics
University of Turin
Piazza Polonia 94
Italy
Name/email consistency: high
- Hair changes in congenital disorders of glycosylation (CDG type 1). Silengo, M., Valenzise, M., Pagliardini, S., Spada, M. Eur. J. Pediatr. (2003)
- A possible relationship between Beckwith-Wiedemann syndrome and prune belly syndrome. Silengo, M., Barberis, L., Ferrero, G.B., Sorasio, L., Valenzise, M. Clin. Dysmorphol. (2002)
- Low birth-weight, microcephalic malformation syndrome in a 46,XX girl and her 46,XY sister with agonadism: third report of the Kennerknecht syndrome or autosomal recessive Seckel-like syndrome with previously undescribed genital anomalies. Silengo, M., Del Monaco, A., Linari, A., Lala, R. Am. J. Med. Genet. (2001)
- New clinical findings in oculo-ectodermal syndrome. Silengo, M., Lerone, M., Seri, M., Priolo, M., Jarre, L. Clin. Dysmorphol. (2000)
- Lower extremity counterpart of the Poland syndrome. Silengo, M., Lerone, M., Seri, M., Boffi, P. Clin. Genet. (1999)