Ricerca
« Pagina precedente |
1 - 10 di 18
|
Pagina successiva »
Risultati della ricerca
Seleziona un immagine per l'avvio del slideshow
Investigating the contribution of coding de novo mutations to orofacial clefts
1 di 10
Identification of Modifying Genes Associated with Fragile X Disorders Using TWAS
2 di 10
Uncovering the contribution of rare genetic variants in orofacial clefts
3 di 10
The Epigenetics of Aging: Exploring Biomarkers and the Interplay Within the Aging Epigenome
4 di 10
Novel Statistical Methods for Analyzing Next Generation Sequencing
Data
5 di 10
Genetic variation in Down syndrome associated congenital heart
defects
6 di 10
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.
7 di 10
Statistical Methods for Rare-Variant Sequencing Studies in
Pedigrees
8 di 10
Genomics of Down Syndrome Associated Congenital Heart Defects
9 di 10
Development of Novel Analytic Methods for Improved Gene Mapping of Complex Human Traits
10 di 10