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An atypical 12q24.31 microdeletion implicates six genes including a histone demethylase KDM2B and a histone methyltransferase SETD1B in syndromic intellectual disability

Labonne, Jonathan D. J.; Lee, Kang-Han; Iwase, Shigeki; Kong, Il-Keun; Diamond, Michael P.; Layman, Lawrence C.; Kim, Cheol-Hee; Kim, Hyung-Goo

ArticleIssue Date2016CitationHUMAN GENETICS, v.135, no.7, pp 757 - 771PublisherSPRINGER
SCIESCOPUS
Comparative deletion mapping at 1p31.3p32.2 implies NFIA responsible for intellectual disability coupled with macrocephaly and the presence of several other genes for syndromic intellectual disabilityopen access

Labonne, Jonathan D. J.; Shen, Yiping; Kong, Il-Keun; Diamond, Michael P.; Layman, Lawrence C.; Kim, Hyung-Goo

ArticleIssue Date2016CitationMOLECULAR CYTOGENETICS, v.9PublisherBMC
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