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Difficulty in genetic counseling of an asymptomatic carrier woman with a de novo 15q13.2q13.3 microdeletion encompassing CHRNA7 and OTUD7A and recurrent 15q13.2q13.3 microdeletion in the fetus

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  • معلومة اضافية
    • بيانات النشر:
      Elsevier, 2025.
    • الموضوع:
      2025
    • Collection:
      LCC:Gynecology and obstetrics
    • File Description:
      electronic resource
    • ISSN:
      1028-4559
    • Relation:
      http://www.sciencedirect.com/science/article/pii/S1028455924002985; https://doaj.org/toc/1028-4559
    • الرقم المعرف:
      10.1016/j.tjog.2024.10.004
    • الرقم المعرف:
      edsdoj.05680c22e9c445948774cf2399b238e2