Skip navigation

Official websites use .gov
A .gov website belongs to an official government organization in the United States.

Secure .gov websites use HTTPS
A lock ( ) or https:// means you’ve safely connected to the .gov website. Share sensitive information only on official, secure websites.

Results 1 - 10 of 46 for Intellectual "disability," "X-linked" 20
  1. ... involved in neuronal differentiation. Cell Res. 2010 Aug;20(8):908-18. doi: 10.1038/cr.2010.81. Epub 2010 Jun 15. Citation on PubMed
  2. ... Med Genet A. 2013 Sep;161A(9):2316-20. doi: 10.1002/ajmg.a.36116. Epub 2013 Jul ... intellectual disability (Snyder-Robinson syndrome). Methods Mol Biol. 2011;720: ...
  3. ... microcephaly with pontine and cerebellar hypoplasia (MICPCH), and X-linked intellectual disability (XL-ID) with or without nystagmus. Within each ... intellectual deficit, Najm type Genetic Testing Registry: Syndromic ... Najm type CASK-Related Disorders National Organization for ...
  4. ... proteins: insights into the molecular pathology of FRAXE intellectual disability. Hum Mol Genet. 2011 May 15;20(10):1873-85. doi: 10.1093/hmg/ddr069. ...
  5. ... the PHF8 gene have been found to cause X-linked intellectual disability, Siderius type. This condition is characterized by mild ... cleft lip and palate found in males with X-linked intellectual disability, Siderius type. More About This Health Condition histone ...
  6. ... the X chromosome, this condition is known as X-linked intellectual disability (XLID) or sometimes nonsyndromic XLID. XLID can occur ... screening of ARX gene in Iranian families with X-linked intellectual disability. Arch Iran Med. 2012 Jun;15(6):361- ...
  7. ... gene have also been found in individuals with X-linked intellectual disability. These individuals have delayed development and other neurological ... A noncoding, regulatory mutation implicates HCFC1 in nonsyndromic intellectual ... Epub 2012 Sep 20. Citation on PubMed or Free article on PubMed ...
  8. ... in the HSD17B10 gene causes a form of X-linked intellectual disability called MRXS10. This disorder is characterized by intellectual ...
  9. ... proteins: insights into the molecular pathology of FRAXE intellectual disability. Hum Mol Genet. 2011 May 15;20(10):1873-85. doi: 10.1093/hmg/ddr069. ...
  10. ... autosomal recessive cutis laxa can have delayed development, intellectual disability, seizures, problems with movement, or eye or bone abnormalities.The X-linked form of cutis laxa is often called occipital ...
previous · 1 · 2 · 3 · 4 · 5 · next