Related Experiment Video
Updated: Jun 28, 2026

Chromosome Replicating Timing Combined with Fluorescent In situ Hybridization
Published on: December 10, 2012
Terminal deletion of chromosome 6q
Pen-Hua Su1, Jia-Yuh Chen, Suh-Jen Chen
1Department of Pediatrics, Division of Neonatology, Chung Shan Medical University Hospital, Taichung, Taiwan.
Abstract:
Terminal deletions of chromosome 6q are rare. Clinical features associated with 6q terminal deletion syndrome include psychomotor retardation, seizures, hypotonia, short neck, and facial abnormalities, as well as various case-specific anomalies. Here, we describe a girl with 6q terminal deletion syndrome and unusually short stature. Features of previously described patients are also summarized.
Related Concept Videos
Inheritance of Chromatin Structures
Karyotyping
Karyotyping
Separation of Sister Chromatids
At the onset of anaphase, separase, a proteolytic enzyme, is...
Separation of Sister Chromatids
At the onset of anaphase, separase, a proteolytic enzyme, is...
Chromosome Duplication
The basic unit of the chromatin is the nucleosome, consisting of DNA wrapped around octameric histone proteins and short stretches of linker DNA separating individual nucleosomes. The histone proteins within the nucleosome have their...

