Mental Retardation, X-Linked

Known as: X-Linked Mental Retardation Syndromes, Mental Retardation, X Linked, Retardation, X-Linked Mental 
A class of genetic disorders resulting in INTELLECTUAL DISABILITY that is associated either with mutations of GENES located on the X CHROMOSOME or… (More)
National Institutes of Health

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
Highly Cited
2010
Highly Cited
2010
Hyperphosphatasia mental retardation (HPMR) syndrome is an autosomal recessive form of mental retardation with distinct facial… (More)
  • table 5
Is this relevant?
Highly Cited
2009
Highly Cited
2009
Although autosomal forms of nonsyndromic mental retardation account for the majority of cases of mental retardation, the genes… (More)
  • table 1
  • table 2
Is this relevant?
Highly Cited
2008
Highly Cited
2008
Mediator occupies a central role in RNA polymerase II transcription as a sensor, integrator, and processor of regulatory signals… (More)
  • figure 1
  • figure 2
  • figure 3
  • figure 4
  • figure 5
Is this relevant?
Highly Cited
2008
Highly Cited
2008
Mental retardation (MR) is the most frequent handicap among children and young adults. Although a large proportion of X-linked MR… (More)
  • figure 1
  • figure 2
  • figure 3
  • figure 4
  • figure 5
Is this relevant?
2008
2008
INTRODUCTION We identified a female patient with mental retardation and sensory hyperarousal. She has a de novo paracentric… (More)
Is this relevant?
Highly Cited
2007
Highly Cited
2007
Mice lacking expression of the fragile X mental retardation 1 (Fmr1) gene have deficits in types of learning that are dependent… (More)
  • figure 1
  • figure 2
  • figure 3
  • figure 4
  • figure 6
Is this relevant?
Highly Cited
2004
Highly Cited
2004
Fragile X mental retardation 1 (Fmr1) is a highly conserved gene with major roles in CNS structure and function. Its product, the… (More)
  • figure 1
  • figure 2
  • figure 3
  • figure 4
  • figure 6
Is this relevant?
Review
2004
Review
2004
Data on the relationships between cognitive and physical phenotypes, and a deficit of fragile X mental retardation 1 (FMR1) gene… (More)
Is this relevant?
Highly Cited
2002
Highly Cited
2002
Some deleterious X-linked mutations may result in a growth disadvantage for those cells in which the mutation, when on the active… (More)
Is this relevant?
Highly Cited
2002
Highly Cited
2002
A 4-base pair deletion in the neuronal serine protease neurotrypsin gene was associated with autosomal recessive nonsyndromic… (More)
Is this relevant?