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High Resolution X Chromosome Copy Number Variation in Autism
1 de 10
Associations Between Perinatal Exposures and Neonatal DNA
Methylation
2 de 10
A Biochemical Model of Hybridization on DNA Microarrays and its Application to Single Nucleotide Polymorphism and Copy Number Variation Genotyping in Trisomy 21 Individuals
3 de 10
Genetic variation in Down syndrome associated congenital heart
defects
4 de 10
Stem cell derived monkey neural progenitor cells as a platform for translational research in Huntington's disease
5 de 10
MeCP2 Mediated Regulation of Small Noncoding RNA
6 de 10
Genetic variation caused by active retrotransposons in the humangenome
7 de 10
Identification of Aberrantly Expressed Synaptic Proteins in the
Mouse Model of Fragile X Syndrome
8 de 10
Assessment of the clinical impact of sequence variants in the
FMR1 gene
9 de 10
Pathogenesis of novel FMR1 mutations in fragile X syndrome
10 de 10