Paternal Uniparental Disomy 11p15.5 in the Pancreatic Nodule of an Infant With Costello Syndrome: Shared Mechanism for Hyperinsulinemic Hypoglycemia in Neonates With Costello and Beckwith–Wiedemann Syndrome and Somatic Loss of Heterozygosity in Costello Syndrome Driving Clonal Expansion

Những quyển sách tương tự

• Mosaic uniparental disomy in Beckwith-Wiedemann syndrome.
  Bằng: Slatter, R E, et al.
  Được phát hành: (1994)
• Paternal Uniparental Disomy of the Entire Chromosome 20 in a Child with Beckwith-Wiedemann Syndrome
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  Được phát hành: (2021)
• Somatic Mosaicism for Paternal Uniparental Disomy of 11p15.5 Region in Adrenal and Liver Tissues in a Newborn with Atypical Beckwith–Wiedemann Syndrome
  Bằng: Urzua, Abraham, et al.
  Được phát hành: (2019)
• Genome-wide paternal uniparental disomy mosaicism in a woman with Beckwith–Wiedemann syndrome and ovarian steroid cell tumour
  Bằng: Gogiel, Magdalena, et al.
  Được phát hành: (2013)
• Paternal Uniparental Disomy with Segmental Loss of Heterozygosity of Chromosome 11 are Hallmark Characteristics of Syndromic and Sporadic Embryonal Rhabdomyosarcoma
  Bằng: Robbins, Katherine M., et al.
  Được phát hành: (2016)