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High Resolution X Chromosome Copy Number Variation in Autism
1 di 10
Genomics studies of population structure and evolution in Neisseria gonorrhoeae
2 di 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 di 10
Genetic variation in Down syndrome associated congenital heart
defects
4 di 10
Assessment of cis and trans-acting factors for involvement in the
altered recombination patterns associated with Trisomy 21
5 di 10
Assessment of the clinical impact of sequence variants in the
FMR1 gene
6 di 10
Effects of Life History and Genome Architecture on ssRNA Virus
Evolution and Extinction
7 di 10
An Investigation of the Properties of Gene-Based Tests of GWAS Data: Simulations and Analyses of ADHD GWAS Data
8 di 10
Genomics of Down Syndrome Associated Congenital Heart Defects
9 di 10
Identifying Variants in Neuroligin Pathway Genes Using Next
Generation Sequencing Technologies
10 di 10