Occurrence and clinical features of epileptic and non-epileptic paroxysmal events in five children with Pallister–Killian syndrome
Author:
Publisher
Elsevier BV
Subject
Genetics (clinical),Genetics,General Medicine
Reference34 articles.
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3. Isochromosome 12p mosaicism (Pallister mosaic aneuploidy or Pallister-Killian syndrome): report of 11 cases;Reynolds;Am. J. Med. Genet.,1987
4. Pallister-Killian syndrome: a Mild case diagnosed by fluorescene in situ hybridization. Review of the literature and expansion of the phenotype;Bielanska;Am. J. Med. Genet.,1996
5. Pallister-Killian syndrome: characterization of the isochromosome 12p by fluorescent in situ hybridization;Speleman;Am. J. Med. Genet.,1991
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1. Structural brain abnormalities in Pallister-Killian syndrome: a neuroimaging study of 31 children;Orphanet Journal of Rare Diseases;2024-03-08
2. Case Report: A Case Study on the Neurodevelopmental Profile of a Child With Pallister–Killian Syndrome and His Unaffected Twin;Frontiers in Pediatrics;2022-03-15
3. Prenatal diagnosis of Pallister‐Killian syndrome and literature review;Journal of Cellular and Molecular Medicine;2021-08-18
4. Pallister–Killian Syndrome versus Trisomy 12p—A Clinical Study of 5 New Cases and a Literature Review;Genes;2021-05-26
5. Clinical Variability of Pallister–Killian Syndrome in Two Egyptian Patients;Journal of Pediatric Genetics;2019-11-21
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