Muskuläre Hypotonie, Gedeihstörung und auffälliges Lippenrot beim Neugeborenen
Author:
Publisher
Springer Science and Business Media LLC
Subject
Surgery,Pediatrics, Perinatology and Child Health
Link
https://link.springer.com/content/pdf/10.1007/s00112-021-01186-w.pdf
Reference4 articles.
1. Alqahtani AS, Putoux A, Bonnet Dupeyron MN et al (2019) Postnatal clinical phenotype of five patients with Pallister-Killian Syndrome (tetrasomy 12p): Interest of array CGH for diagnosis and review of the literature. Mol Genet Genomic Med 7:e939. https://doi.org/10.1002/mgg3.939
2. Izumi K, Krantz ID (2014) Pallister-Killian syndrome. Am J Med Genet C Semin Med Genet 166C:406–413. https://doi.org/10.1002/ajmg.c.31423
3. Karaman B, Kayserili H, Ghanbari A, Uyguner ZO, Toksoy G, Altunoglu U, Basaran S (2018) Pallister-Killian syndrome: clinical, cytogenetic and molecular findings in 15 cases. Mol Cytogenet 11:45. https://doi.org/10.1186/s13039-018-0395-z
4. Wilkens A, Liu H, Park K, Campbell LB, Jackson M, Kostanecka A, Pipan M, Izumi K, Pallister P, Krantz ID (2012) Novel clinical manifestations in Pallister-Killian syndrome: comprehensive evaluation of 59 affected individuals and review of previously reported cases. Am J Med Genet A 158A(12):3002–3017. https://doi.org/10.1002/ajmg.a.35722
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