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Pallister-Killian syndrome: a report of 2 cases and review of its surgical aspects

โœ Scribed by Maciej Baglaj; Juliette King; Robert Carachi


Book ID
116687205
Publisher
Elsevier Science
Year
2008
Tongue
English
Weight
202 KB
Volume
43
Category
Article
ISSN
0022-3468

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Parental origin of the isochromosome 12p
โœ Struthers, J.L.; Cuthbert, C.D.; Khalifa, M.M. ๐Ÿ“‚ Article ๐Ÿ“… 1999 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 36 KB ๐Ÿ‘ 2 views

Pallister-Killian syndrome (PKS) is characterized by multiple congenital anomalies including pigmentary skin changes, mental retardation, and the mosaic presence of a tissue-limited isochromosome 12p [i(12p)]. Mechanism(s) of formation and parental origin of the isochromosome are not well understood