Identification of a rare copy number polymorphic gain at 3q12.2 with candidate genes for familial endometriosis
Abstract Endometriosis is a complex disease that affects 10-15% of women of reproductive age. Familial studies show that relatives of affected patients have a higher risk of developing the disease, implicating a genetic role for this disorder. Little is known about the impact of germline genomic cop...
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| Main Authors: | , , , , , , , , |
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| Format: | Book |
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Federação Brasileira das Sociedades de Ginecologia e Obstetrícia,
2024-05-01T00:00:00Z.
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