Absence of learning difficulties in a hyperactive boy with a terminal Xp deletion encompassing the MRX49 locus

J Med Genet. 2001 Jul;38(7):466-70. doi: 10.1136/jmg.38.7.466.
No abstract available

Publication types

  • Case Reports
  • Letter

MeSH terms

  • Abnormalities, Multiple / genetics*
  • Attention Deficit Disorder with Hyperactivity / complications
  • Attention Deficit Disorder with Hyperactivity / genetics
  • Child
  • Child, Preschool
  • Chromosome Breakage / genetics
  • Chromosome Deletion*
  • Chromosome Mapping
  • Female
  • Genetic Linkage / genetics
  • Genotype
  • Humans
  • Ichthyosis / complications
  • Ichthyosis / genetics*
  • In Situ Hybridization, Fluorescence
  • Infant
  • Infant, Newborn
  • Intellectual Disability / genetics*
  • Karyotyping
  • Learning Disabilities / genetics*
  • Male
  • Phenotype
  • Psychomotor Agitation / complications
  • Psychomotor Agitation / genetics*
  • Translocation, Genetic / genetics
  • X Chromosome / genetics*
  • Y Chromosome / genetics