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Publications
171
A common frameshift mutation and other variants in GJB4 (connexin 30.3): Analysis of hearing impairment families
Authors:
Nuria Lopez-Bigas
,
Salvatore Melchionda
,
Paolo Gasparini
…
Characterization of a novel 21-kb deletion, CFTRdele2,3(21 kb), in the CFTR gene: a cystic fibrosis mutation of Slavic origin common in Central and East Europe
Authors:
T DORK
,
M Macek Jr
,
F. Mekus
…
The mouse brain transcriptome by SAGE: differences in gene expression between P30 brains of the partial trisomy 16 mouse model of Down syndrome (Ts65Dn) and normals
Authors:
R Chrast
,
HS Scott
,
MP Papasavvas
…
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X. Estivill
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