Developmental delay and dysmorphic features associated with a previously undescribed deletion on chromosome 1.

Gelijkaardige items

• Deletion of 8q24 in an Adult with Mild Dysmorphic Features, Developmental Delay, and Ketotic Hypoglycemia
  door: Solomon, Benjamin D., et al.
  Gepubliceerd in: (2010)
• Three Supernumerary Marker Chromosomes in a Patient with Developmental Delay, Mental Retardation, and Dysmorphic Features
  door: Hu, Jie, et al.
  Gepubliceerd in: (2011)
• A recurrent deletion on chromosome 2q13 is associated with developmental delay and mild facial dysmorphisms
  door: Hladilkova, Eva, et al.
  Gepubliceerd in: (2015)
• Partial deletion of chromosome 6p causing developmental delay and mild dysmorphisms in a child: molecular and developmental investigation and literature search
  door: Vrachnis, Nikolaos, et al.
  Gepubliceerd in: (2021)
• Clinical and Molecular Cytogenetic Characterisation of Children with Developmental Delay and Dysmorphic Features
  door: BERTOK, Sara, et al.
  Gepubliceerd in: (2015)