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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
Genomics of Down Syndrome Associated Congenital Heart Defects
5 of 17
Assessment of the clinical impact of sequence variants in the
FMR1 gene
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Assessment of cis and trans-acting factors for involvement in the
altered recombination patterns associated with Trisomy 21
7 of 17
The Origin and Spread of Drug Resistant Malaria in South America
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Telomere length: implications on the risk for chromosome 21
nondisjunction in oocytes
9 of 17
Population Genetics of Raccoons in the Eastern United States With
Implications for Rabies Transmission and Spread
10 of 17
Genetic variation in Down syndrome associated congenital heart
defects
11 of 17
The Role of Insulators and Transcription Factors in Genome
Organization and Function in Drosophila
12 of 17
High Resolution X Chromosome Copy Number Variation in Autism
13 of 17
Evolution of Purine Metabolism
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Sequence analysis of chromosome translocations in neurodevelopmental disorders
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Development of Novel Analytic Methods for Improved Gene Mapping of Complex Human Traits
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A Biochemical Model of Hybridization on DNA Microarrays and its Application to Single Nucleotide Polymorphism and Copy Number Variation Genotyping in Trisomy 21 Individuals
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