Screening for Intellectual Disability Using High-Resolution CMA Technology in a Retrospective Cohort from Central Brazil

Παρόμοια τεκμήρια

• The Identification of Microdeletion and Reciprocal Microduplication in 22q11.2 Using High-Resolution CMA Technology
  ανά: Leite, Ana Julia Cunha, κ.ά.
  Έκδοση: (2016)
• A non-syndromic intellectual disability associated with a de novo microdeletion at 7q and 18p, microduplication at Xp, and 18q partial trisomy detected using chromosomal microarray analysis approach
  ανά: Pinto, Irene Plaza, κ.ά.
  Έκδοση: (2014)
• Molecular Characterization of Koolen De Vries Syndrome in Two Girls with Idiopathic Intellectual Disability from Central Brazil
  ανά: Nascimento, Gustavo R., κ.ά.
  Έκδοση: (2017)
• Diagnostic yield of patients with undiagnosed intellectual disability, global developmental delay and multiples congenital anomalies using karyotype, microarray analysis, whole exome sequencing from Central Brazil.
  ανά: Ana Julia da Cunha Leite, κ.ά.
  Έκδοση: (2022-01-01)
• Mosaic Tetrasomy of 9p24.3q21.11 postnatally identified in an infant born with multiple congenital malformations: a case report
  ανά: Pinto, Irene Plaza, κ.ά.
  Έκδοση: (2018)