Syndromes with lissencephaly. I: Millerdieker and Norman-Roberts syndromes and isolated lissencephaly
Author:
Publisher
Wiley
Subject
Genetics (clinical)
Reference36 articles.
1. Familial lissencephaly with extreme neopallial hypoplasia
2. Partial trisomy of the short arm of chromosome 7 due to a familial translocation rcp(7;14) (p11;p11)
3. An infant with ring 17 chromosome and unusual dermatoglyphs: a new syndrome?
4. A case of partial trisomy 8p resulting from a maternal balanced translocation
5. Pachygyria
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1. Total callosotomy ameliorates epileptic activity and improves cognitive function in a patient with Miller-Dieker syndrome;Epilepsy & Behavior Reports;2024
2. Congenital Malformations of the Central Nervous System;Avery's Diseases of the Newborn;2024
3. Brain Pathways in LIS1-Associated Lissencephaly Revealed by Diffusion MRI Tractography;Brain Sciences;2023-11-29
4. Acute Bowel Ischemia in a Premature Neonate with Miller-Dieker Syndrome and Anomalous Right Coronary Artery From the Pulmonary Artery;Pediatric Annals;2023-08
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