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Chromosome 22q11.21 and 11p15.4 microdeletions confirmed by high‐throughput sequencing analysis in one patient with asymmetric cry syndrome: Case report and review of the literature

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اقرأ أكثر حفظ في قائمتي
  • معلومة اضافية
    • بيانات النشر:
      Wiley, 2021.
    • الموضوع:
      2021
    • نبذة مختصرة :
      Healthcare providers treating newborns with asymmetric cry syndrome should consider 22q11.2 microdeletion within the differential diagnosis list and order appropriate genetic testing.
    • ISSN:
      2050-0904
    • الرقم المعرف:
      10.1002/ccr3.4072
    • Rights:
      OPEN
    • الرقم المعرف:
      edsair.doi.dedup.....0e46d753d2b2ba1b2a5c735ab5c55af2