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Genomic analysis using high-resolution single nucleotide polymorphism arrays reveals novel microdeletions associated with premature ovarian failure
OBJECTIVE: To analyze DNA from women with premature ovarian failure (POF) for genome-wide copy number variations (CNVs), focusing on novel autosomal microdeletions. DESIGN: Case-control genetic association study. SETTING: Department of Obstetrics and Gynecology, Baylor College of Medicine, Houston,...
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| Autors principals: | , , , , , |
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| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
2011
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3062633/ https://ncbi.nlm.nih.gov/pubmed/21256485 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.fertnstert.2010.12.052 |
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