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High Resolution X Chromosome Copy Number Variation in Autism
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Genetic variation in Down syndrome associated congenital heart
defects
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Telomere length: implications on the risk for chromosome 21
nondisjunction in oocytes
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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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Genomics of Down Syndrome Associated Congenital Heart Defects
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Development of Novel Analytic Methods for Improved Gene Mapping of Complex Human Traits
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Identifying Variants in Neuroligin Pathway Genes Using Next
Generation Sequencing Technologies
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Genetic Variation in Recombination as a Risk Factor for
Nondisjunction
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