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- Genomewide analysis of copy number variants in alopecia areata in a Central European cohort reveals association with <i>MCHR2</i>
- Integrative analysis of rare copy number variants and gene expression data in alopecia areata implicates an aetiological role for autophagy
- De novo single-nucleotide and copy number variation in discordant monozygotic twins reveals disease-related genes
- Genomic Analysis of Trichotillomania
- Compilation of a comprehensive gene panel for systematic assessment of genes that govern an individual’s drug responses
- Male infertility and genitourinary birth defects: there is more than meets the eye
- Ottawa, Ontario, Canada, February 13–16, 2013
- Mutational spectrum in 101 patients with hypohidrotic ectodermal dysplasia and breakpoint mapping in independent cases of rare genomic rearrangements
- Androgen Receptor Copy Number Variation and Androgenetic Alopecia: A Case-Control Study
- Identification of Candidate Genes for Min Pig Villi Hair Traits by Genome-Wide Association of Copy Number Variation
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