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BMJ Publishing Group, Journal of Medical Genetics, p. jmedgenet-2015-103184
DOI: 10.1136/jmedgenet-2015-103184
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IntragenicKANSL1mutations and chromosome 17q21.31 deletions: broadening the clinical spectrum and genotype–phenotype correlations in a large cohort of patients
Journal article published in 2015 by
Marcella Zollino,
Giuseppe Marangi,
Emanuela Ponzi,
Daniela Orteschi,
Stefania Ricciardi,
Serena Lattante,
Marina Murdolo,
Domenica Battaglia,
Ilaria Contaldo 
,
Eugenio Mercuri,
Maria Chiara Stefanini,
Roseline Caumes,
Patrick Edery,
Massimiliano Rossi,
Maria Piccione
and other authors.
,
Eugenio Mercuri,
Maria Chiara Stefanini,
Roseline Caumes,
Patrick Edery,
Massimiliano Rossi,
Maria Piccione
and other authors.
This paper is available in a repository.
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