A 15q25.2 microdeletion phenotype for premature ovarian failure in a Chinese girl: a case report and review of literature
Abstract Background Proximal microdeletions on chromosome 15q25.2 are very rare, and are associated with neurodevelopmental delay, inguinal hernia, chest deformities, and anemia. The minimum length missed so far is 1.4 Mb. However, there were no cases reported till date on microdeletions at position...
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| Main Authors: | , , , |
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| Format: | Book |
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BMC,
2020-09-01T00:00:00Z.
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| Call Number: |
A1234.567 |
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