| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 8958369 | Journal of Pediatric and Adolescent Gynecology | 2018 | 13 Pages |
Abstract
Our purpose is to underscore the possible presence of gynecological malformations in patients with 16p11.2 microdeletion and highlight the utility of a genetic evaluation in cases of MRKH syndrome.
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Authors
Marta MD, Gianluca MD, Silvia MD, Claudia MD, Susanna PhD, Paola PhD, Donatella MD,