A Biochemical Model of Hybridization on DNA Microarrays and its Application to Single Nucleotide Polymorphism and Copy Number Variation Genotyping in Trisomy 21 Individuals

Genetic variation in Down syndrome associated congenital heart defects

Assessment of cis and trans-acting factors for involvement in the altered recombination patterns associated with Trisomy 21

Assessment of the clinical impact of sequence variants in the FMR1 gene

Genomics of Down Syndrome Associated Congenital Heart Defects

Identifying Variants in Neuroligin Pathway Genes Using Next Generation Sequencing Technologies

Genetic and environmental contributions to gastrointestinal health

Genetic Variation in Recombination as a Risk Factor for Nondisjunction