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Genetic Variation in Recombination as a Risk Factor for
Nondisjunction
1 of 17
Genetic and environmental contributions to gastrointestinal health
2 of 17
Identifying Variants in Neuroligin Pathway Genes Using Next
Generation Sequencing Technologies
3 of 17
Novel Germline and Somatic Retrotransposon Insertions in
Humans
4 of 17
Evolution of Purine Metabolism
5 of 17
Development of Novel Analytic Methods for Improved Gene Mapping of Complex Human Traits
6 of 17
Genomics of Down Syndrome Associated Congenital Heart Defects
7 of 17
Assessment of the clinical impact of sequence variants in the
FMR1 gene
8 of 17
Assessment of cis and trans-acting factors for involvement in the
altered recombination patterns associated with Trisomy 21
9 of 17
The Origin and Spread of Drug Resistant Malaria in South America
10 of 17
Telomere length: implications on the risk for chromosome 21
nondisjunction in oocytes
11 of 17
Population Genetics of Raccoons in the Eastern United States With
Implications for Rabies Transmission and Spread
12 of 17
Genetic variation in Down syndrome associated congenital heart
defects
13 of 17
A Biochemical Model of Hybridization on DNA Microarrays and its Application to Single Nucleotide Polymorphism and Copy Number Variation Genotyping in Trisomy 21 Individuals
14 of 17
The Role of Insulators and Transcription Factors in Genome
Organization and Function in Drosophila
15 of 17
Sequence analysis of chromosome translocations in neurodevelopmental disorders
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High Resolution X Chromosome Copy Number Variation in Autism
17 of 17