DOCTORATE in GENETICS, ONCOLOGY and CLINICAL MEDICINE (GenOMeC)
DOTTORATO DI RICERCA IN
GENETICA ONCOLOGIA E MEDICINA CLINICA
UNIVERSITA' DEGLI STUDI DI SIENA
Home Page |
Publications
during the PhD program |
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Spanhol-Rosseto Ariele |
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1)
Novel FOXG1 mutations associated with the
congenital variant of Rett syndrome.
Mencarelli MA, Spanhol-Rosseto A, Artuso R,
Rondinella D, De Filippis R, Bahi-Buisson N, Nectoux J, Rubinsztajn R,
Bienvenu T, Moncla A, Chabrol B, Villard L, Krumina Z, Armstrong J,
Roche A, Pineda M, Gak E, Mari F, Ariani F, Renieri A.
J Med Genet.
2010 Jan;47(1):49-53 |
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2)
FOXG1 is responsible for the congenital variant of
Rett syndrome.
Ariani F, Hayek G, Rondinella D, Artuso R,
Mencarelli MA, Spanhol-Rosseto A, Pollazzon M, Buoni S, Spiga O,
Ricciardi S, Meloni I, Longo I, Mari F, Broccoli V, Zappella M, Renieri
A.
Am J Hum
Genet. 2008 Jul;83(1):89-93 |
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