Materias dentro de su búsqueda.
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Article
Female
4
Humans
4
Male
Sanger sequencing
4
disease severity
4
epilepsy
exon
4
family history
4
female
4
gene deletion
4
genetic variability
4
genetics
4
heterozygosity
4
human
4
intellectual impairment
4
male
4
missense mutation
4
mosaicism
4
sequence analysis
4
stop codon
4
ARX gene
2
Argentina
2
Autism Spectrum Disorder
2
Base Sequence
2
Child
2
Child, Preschool
2
Cohort Studies
2
DCX gene
2
DNA Copy Number Variations
2
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1por Nemirovsky, Sergio I., Ogara, Maria Florencia, Pecci, Adali, Martí, Marcelo Adrián, Vazquez, Martín Pablo, Turjanski, Adrián GustavoMaterias: “...epilepsy...”
Publicado 2015
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2por Nemirovsky, S.I., Córdoba, M., Zaiat, J.J., Completa, S.P., Vega, P.A., González-Morón, D., Medina, N.M., Fabbro, M., Romero, S., Brun, B., Revale, S., Ogara, M.F., Pecci, A., Marti, M., Vazquez, M., Turjanski, A., Kauffman, M.A.Materias: “...epilepsy...”
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3Publicado 2017Materias: “...epilepsy...”
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4por González-Morón, D., Vishnopolska, S., Consalvo, D., Medina, N., Marti, M., Córdoba, M., Vazquez-Dusefante, C., Claverie, S., Rodríguez-Quiroga, S.A., Vega, P., Silva, W., Kochen, S., Kauffman, M.A.Materias: “...epilepsy...”
JOUR