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A genome-wide screen for copy number alterations in an adolescent pilot cohort with Müllerian anomalies
OBJECTIVE: To examine whether pathogenic CNCs can be identified in DNA from females with different classes of Müllerian anomalies. DESIGN: We conducted array-based CNV analysis using an oligonucleotide array from DNA in 12 adolescent females with different types of Müllerian anomalies. SETTING: Univ...
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| Publicat a: | Fertil Steril |
|---|---|
| Autors principals: | , , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
2014
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4476902/ https://ncbi.nlm.nih.gov/pubmed/25492685 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.fertnstert.2014.10.044 |
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