Intragenic KANSL1 mutations and chromosome 17q21.31 deletions: broadening the clinical spectrum and genotype-phenotype correlations in a large cohort of patients. (Q52912983)
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scientific article published on 30 September 2015
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English | Intragenic KANSL1 mutations and chromosome 17q21.31 deletions: broadening the clinical spectrum and genotype-phenotype correlations in a large cohort of patients. |
scientific article published on 30 September 2015 |
Statements
Intragenic KANSL1 mutations and chromosome 17q21.31 deletions: broadening the clinical spectrum and genotype-phenotype correlations in a large cohort of patients. (English)
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Marcella Zollino
Giuseppe Marangi
Emanuela Ponzi
Daniela Orteschi
Stefania Ricciardi
Serena Lattante
Marina Murdolo
Domenica Battaglia
Maria Chiara Stefanini
Roseline Caumes
Patrick Edery
Massimiliano Rossi
Maria Piccione
Giovanni Corsello
Matteo Della Monica
Francesca Scarano
Manuela Priolo
Mattia Gentile
Giuseppe Zampino
Raymon Vijzelaar
Omar Abdulrahman
Beatrice Oneda
Matthew A Deardorff
Sulagna C Saitta
Holly Dubbs
30 September 2015
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