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LAMM syndrome with middle ear dysplasia associated with compound heterozygosity for FGF3 mutations
Sensi, Alberto, Ceruti, Stefano, Trevisi, Patrizia, Gualandi, Francesca, Busi, Micol, Donati, Ilaria, Neri, Marcella, Ferlini, Alessandra, Martini, Alessandro
Published in American journal of medical genetics. Part A (01.05.2011)
Published in American journal of medical genetics. Part A (01.05.2011)
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Journal Article
Fgf3-Fgf4-cis: A new mouse line for studying Fgf functions during mouse development
Anderson, Matthew J., Southon, Eileen, Tessarollo, Lino, Lewandoski, Mark
Published in Genesis (New York, N.Y. : 2000) (01.02.2016)
Published in Genesis (New York, N.Y. : 2000) (01.02.2016)
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Journal Article
Homozygous FGF3 mutations result in congenital deafness with inner ear agenesis, microtia, and microdontia
Tekin, M, Öztürkmen Akay, H, Fitoz, S, Birnbaum, S, Cengiz, FB, Sennaroğlu, L, İncesulu, A, Yüksel Konuk, EB, Hasanefendioğlu Bayrak, A, Şentürk, S, Cebeci, İ, Ütine, GE, Tunçbilek, E, Nance, WE, Duman, D
Published in Clinical genetics (01.06.2008)
Published in Clinical genetics (01.06.2008)
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Journal Article