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Identification and Evaluation of Novel Epilepsy-Associated Variants
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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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Development of Novel Analytic Methods for Improved Gene Mapping of Complex Human Traits
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Sequence analysis of chromosome translocations in neurodevelopmental disorders
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Evolution of Purine Metabolism
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High Resolution X Chromosome Copy Number Variation in Autism
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The Role of Insulators and Transcription Factors in Genome
Organization and Function in Drosophila
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Genetic variation in Down syndrome associated congenital heart
defects
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Serum Dopamine Beta Hydroxylase (DβH) enzyme activity
changes within individual women according to stage of pregnancy:
Evidence that regulation of expression of DβH differs during
pregnancy in women carrying different genotypes at rs1611115.
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Population Genetics of Raccoons in the Eastern United States With
Implications for Rabies Transmission and Spread
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Telomere length: implications on the risk for chromosome 21
nondisjunction in oocytes
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The Origin and Spread of Drug Resistant Malaria in South America
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Assessment of cis and trans-acting factors for involvement in the
altered recombination patterns associated with Trisomy 21
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Assessment of the clinical impact of sequence variants in the
FMR1 gene
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Mutations in APH(3')-IIIa Increase Activity Against Amikacin
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Genomics of Down Syndrome Associated Congenital Heart Defects
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Novel Germline and Somatic Retrotransposon Insertions in
Humans
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Identifying Variants in Neuroligin Pathway Genes Using Next
Generation Sequencing Technologies
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Genetic and environmental contributions to gastrointestinal health
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Genetic Variation in Recombination as a Risk Factor for
Nondisjunction
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