5q31 Microdeletions: Definition of a Critical Region and Analysis of LRRTM2, a Candidate Gene for Intellectual Disability

অনুরূপ উপাদানগুলি

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  প্রকাশিত: (2014)
• KIF11 microdeletion is associated with microcephaly, chorioretinopathy and intellectual disability
  অনুযায়ী: Malvezzi, João VM, অন্যান্য
  প্রকাশিত: (2018)
• Microdeletions in 9q33.3-q34.11 in five patients with intellectual disability, microcephaly, and seizures of incomplete penetrance: is STXBP1 not the only causative gene?
  অনুযায়ী: Ehret, Julia K., অন্যান্য
  প্রকাশিত: (2015)
• Loss-of-function variants of SETD5 cause intellectual disability and the core phenotype of microdeletion 3p25.3 syndrome
  অনুযায়ী: Kuechler, Alma, অন্যান্য
  প্রকাশিত: (2015)
• Single gene microdeletions and microduplication of 3p26.3 in three unrelated families: CNTN6 as a new candidate gene for intellectual disability
  অনুযায়ী: Kashevarova, Anna A, অন্যান্য
  প্রকাশিত: (2014)