Neuropsychological and Language Deficits in 22q11.2 Deletion Syndrome
By: J Gordon Millichap and John J Millichap
References
- Cancrini C Puliafito P Digilio MC Soresina A Martino S Rondelli R Clinical features and follow-up in patients with 22q11.2 deletion syndrome J Pediatr 2014 Jun 164 6 1475 1480.e2 10.1016/j.jpeds.2014.01.056 24657119
- Digilio MC Angioni A De Santis M Lombardo A Giannotti A Dallapiccola B Spectrum of clinical variability in familial deletion 22q11.2: from full manifestation to extremely mild clinical anomalies Clin Genet 2003 Apr 63 4 308 13 10.1016/j.jpeds.2014.01.056 12702165
- Millichap JG Neurological Syndromes : A Clinical Guide to Symptoms and Diagnosis 2013 New York Springer 279 10.1007/978-1-4614-7786-0
DOI: https://doi.org/10.15844/pedneurbriefs-28-7-2 | Journal eISSN: 2166-6482
Language: English
Page range: 50 - 51
Published on: Jul 1, 2014
Published by: Pediatric Neurology Briefs Publishers
In partnership with: Paradigm Publishing Services
Keywords:
© 2014 J Gordon Millichap, John J Millichap, published by Pediatric Neurology Briefs Publishers
This work is licensed under the Creative Commons Attribution 4.0 License.