Pallister-Killian syndrome: clinical, cytogenetic and molecular findings in 15 cases

Pallister Killian syndrome (PKS, OMIM 601803) is a rare genetic disorder with a distinct phenotype caused by tissue- limited mosaicism tetrasomy of the short arm of chromosome 12, which usually cytogenetically...

Source: Molecular Cytogenetics - August 17, 2018 Category: Molecular Biology Authors: Birsen Karaman, H ülya Kayserili, Asadollah Ghanbari, Zehra Oya Uyguner, Güven Toksoy, Umut Altunoglu and Seher Basaran Tags: Research Source Type: research