Norman-Roberts syndrome: Clinical and molecular studies
Author:
Publisher
Wiley
Subject
Genetics(clinical)
Reference19 articles.
1. Diagnostic Features And Clinical Signs Of 21 Patients With Lissencephaly Type I
2. Syndromes with lissencephaly. I: Millerdieker and Norman-Roberts syndromes and isolated lissencephaly
3. Further comments on the lissencephaly syndromes
4. Syndromes with lissencephaly. II: Walker-Warburg and Cerebro-Oculo-Muscular syndromes and a new syndrome with type II lissencephaly
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2. Mutations in tubulin genes are frequent causes of various foetal malformations of cortical development including microlissencephaly;Acta Neuropathologica Communications;2014-07-25
3. A Forensic Autopsy Case of Lissencephaly for Evaluating the Possibility of Child Abuse;Korean Journal of Legal Medicine;2013
4. Malformations of Cortical Development;Swaiman's Pediatric Neurology;2012
5. New trends in neuronal migration disorders;European Journal of Paediatric Neurology;2010-01
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