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Fig. 2 | Molecular Cytogenetics

Fig. 2

From: 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?

Fig. 2

Schematic representation of the microdeletions. Red bars: Microdeletions of patients 1 through 5 are presented. Grey bars: previously published microdeletions. Lower panel: detail with smallest region of overlap (SRO, dashed lines, red box) and RefSeq genes with black arrows showing direction of transcription (green: genes analyzed by expression studies)

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Molecular Cytogenetics

ISSN: 1755-8166