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Hoffmann, R. A wiki for the life sciences where authorship matters. Nature Genetics (2008)

Margherita Silengo

Clinical Genetics

Department of Paediatrics

University of Turin

Piazza Polonia 94



Name/email consistency: high



  • Clinical Genetics, Department of Paediatrics, University of Turin, Piazza Polonia 94, Italy. 2003
  • Dipartimento di Scienze Pediatriche e dell'Adolescenza, Università di Torino, Italy. 1999 - 2002


  1. Hair changes in congenital disorders of glycosylation (CDG type 1). Silengo, M., Valenzise, M., Pagliardini, S., Spada, M. Eur. J. Pediatr. (2003) [Pubmed]
  2. 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) [Pubmed]
  3. 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) [Pubmed]
  4. New clinical findings in oculo-ectodermal syndrome. Silengo, M., Lerone, M., Seri, M., Priolo, M., Jarre, L. Clin. Dysmorphol. (2000) [Pubmed]
  5. Lower extremity counterpart of the Poland syndrome. Silengo, M., Lerone, M., Seri, M., Boffi, P. Clin. Genet. (1999) [Pubmed]
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