Contiguous gene syndrome due to an interstitial deletion in Xp22.3 in a boy with ichthyosis, chondrodysplasia punctata, mental retardation and ADHD.
Academic Article
Publication Date:
2007
Iris type:
1.1 Articolo in rivista
Keywords:
sinrdome da geni contigui; cromosoma X; delezioni
List of contributors:
Lonardo, F; Parenti, G; Luquetti, Dv; Annunziata, I; DELLA MONICA, M; Perone, L; DE GREGORI, M; Zuffardi, Orsetta; BRUNETTI PIERRI, N; Andria, G; Scarano, G.
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