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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.
and other authors.
This paper is available in a repository.
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