Mild phenotype in a 15-year-old boy with Pallister-Killian syndrome
Author:
Publisher
Wiley
Subject
Genetics (clinical)
Reference37 articles.
1. Pallister-Killian syndrome: A mild case diagnosed by fluorescence in situ hybridization. Review of the literature and expansion of the phenotype
2. Pallister-Killian syndrome detected by fluorescence in situ hybridization
3. Prezygotic origin of the isochromosome 12p in Pallister-Killian syndrome
4. ISDN. 1995. In: editor. An international system for human cytogenetics nomenclature. Basel: S. Karger.
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1. Co-Occurrence of Pallister-Killian Syndrome and Burkitt Lymphoma in a Patient with Near-Normal Neurocognitive Development;Molecular Syndromology;2023
2. Less Well-Defined or So Far Unclassifiable Patterns;Mosaicism in Human Skin;2022-11-24
3. 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
4. Case Report: Early Neonatal EEG in Two Infants with Pallister Killian Syndrome (PKS);HRB Open Research;2022-02-18
5. Cognitive, Behavioral, and Sensory Profile of Pallister–Killian Syndrome: A Prospective Study of 22 Individuals;Genes;2022-02-16
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