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High Resolution X Chromosome Copy Number Variation in Autism
1 di 10
Sequence analysis of chromosome translocations in neurodevelopmental disorders
2 di 10
The Role of Insulators and Transcription Factors in Genome
Organization and Function in Drosophila
3 di 10
A Biochemical Model of Hybridization on DNA Microarrays and its Application to Single Nucleotide Polymorphism and Copy Number Variation Genotyping in Trisomy 21 Individuals
4 di 10
Genetic variation in Down syndrome associated congenital heart
defects
5 di 10
Population Genetics of Raccoons in the Eastern United States With
Implications for Rabies Transmission and Spread
6 di 10
Telomere length: implications on the risk for chromosome 21
nondisjunction in oocytes
7 di 10
The Origin and Spread of Drug Resistant Malaria in South America
8 di 10
Assessment of cis and trans-acting factors for involvement in the
altered recombination patterns associated with Trisomy 21
9 di 10
Assessment of the clinical impact of sequence variants in the
FMR1 gene
10 di 10