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Elsevier, European Journal of Medical Genetics, 4(50), p. 301-308

DOI: 10.1016/j.ejmg.2007.04.005

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Contiguous gene syndrome due to an interstitial deletion in Xp22.3 in a boy with ichthyosis, chondrodysplasia punctata, mental retardation and ADHD

Journal article published in 2007 by Fortunato Lonardo ORCID, Giancarlo Parenti, Daniela Varela Luquetti, Ida Annunziata, Matteo Della Monica, Lucia Perone, Manuela De Gregori, Orsetta Zuffardi, Nicola Brunetti-Pierri, Generoso Andria, Gioacchino Scarano ORCID
This paper is available in a repository.
This paper is available in a repository.

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