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Search Results - Lino, A.M.M
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A novel stop codon mutation in the PMP22 gene associated with a variable phenotype
by
Abe, K.T
,
Lino, A.M.M
,
Hirata, M.T.A
,
Pavanello, R.C.M
,
Brotto, M.W.I
,
Marchiori, P.E
,
Zatz, M
Published in
Neuromuscular disorders : NMD
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Optimization methods for optimal transmitter locations in a mobile wireless system
by
Aguado-Agelet, F.
,
Varela, A.M.M.
,
Alvarez-Vazquez, L.J.
,
Hernando, J.M.
,
Formella, A.
Published in
IEEE transactions on vehicular technology
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Ieee Trans. Vehi. Technol
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Neuromuscular Disorders : Nmd
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Adolescent
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Antenna Sectorization
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Charcot-Marie-Tooth Type 1
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Codon, Terminator - Genetics
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Cost Function
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Dna Mutational Analysis - Methods
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