P362: Newborn with 4 syndromes (Down, Turner, Xp11.22 duplication and 3q duplication) characterized by G-banding, FISH, microarray and optical genome mapping

Παρόμοια τεκμήρια

• Prenatally detected six duplications at Xp22.33-p11.22: a case report
  ανά: Xue Zhang, κ.ά.
  Έκδοση: (2023-04-01)
• Turner syndrome due to Xp22.33 deletion combined with 7p22.3 duplication
  ανά: Ha young Jo, κ.ά.
  Έκδοση: (2023-02-01)
• A Rare Novel Copy Number Variation of Xp22.33-p11.22 Duplication is Associated with Congenital Heart Defects
  ανά: Juan Zhang, κ.ά.
  Έκδοση: (2015-01-01)
• Xp11.22 duplications in four unrelated Chinese families: delineating the genotype-phenotype relationship for HSD17B10 and FGD1
  ανά: Qingming Wang, κ.ά.
  Έκδοση: (2020-05-01)
• Acute pre-B lymphoblastic leukemia and congenital anomalies in a child with a de novo 22q11.1q11.22 duplication
  ανά: Vaisvilas M, κ.ά.
  Έκδοση: (2018-10-01)