Diagnostic Features And Clinical Signs Of 21 Patients With Lissencephaly Type I
Author:
Publisher
Wiley
Subject
Clinical Neurology,Developmental Neuroscience,Pediatrics, Perinatology, and Child Health
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1469-8749.1990.tb08431.x/fullpdf
Reference46 articles.
1. Turricéphalie héréditaïre, microcephalie familiale avec lissencephalie. Rapport de ce syndrome malformatif avec les dysraphies cerebro-medullaires;Alberca-Serrano;Journal of Neurological Science,1964
2. Miller-Dieker syndrome: a disorder affecting specific pathways of neuronal migration;Alvarez;Neurology,1986
3. Inverted neurons in agyria. A golgi study of a case with abnormal chromosome 17;Bordarier;Human Genetics,1986
4. An infant with ring 17 chromosome and unusual dermatoglyphs: a new syndrome;Carpenter;Journal of Medical Genetics,1981
5. Lissencephaly: diagnosis by computed tomography and magnetic resonance imaging;Cordes;European Journal of Radiology,1988
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