Cancrini, Caterina, et al. "Clinical features and follow-up in patients with 22q11. 2 deletion syndrome." The Journal of pediatrics 164.6 (2014): 1475-1480.
Year: 2014
Type: article
Authors: Cancrini C, Puliafito P, Digilio MC, Soresina A, Martino S, Rondelli R, et al. Collaborators Pierani P, Gabrielli A, Danieli MG, De Mattia D, Sisto C, Dammacco F, Ranieri G, et al.
Language: English
Subfield: Genetics
Domain: Life Sciences
Open Access status: closed
OpenAlex ID: W7064553637
