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Fig. 4 | Molecular Cytogenetics

Fig. 4

From: Comparative deletion mapping at 1p31.3-p32.2 implies NFIA responsible for intellectual disability coupled with macrocephaly and the presence of several other genes for syndromic intellectual disability

Fig. 4

Transcript levels of six candidate genes involved in CNVs were determined by RT-qPCR. The level of transcripts of DAB1, NFIA and DNAJC6 were markedly reduced in DGDP005 relative to the healthy white female control. Transcripts derived from HOOK1 and DOCK7 were reduced approximately by half, while PDE4B transcripts decreased moderately

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