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Figure 1 | BMC Medical Genetics

Figure 1

From: Identification of a rare 17p13.3 duplication including the BHLHA9 and YWHAEgenes in a family with developmental delay and behavioural problems

Figure 1

A) Family tree that shows the individuals who were available for array-CGH. Some components of the family were reported as being affected by behavioural deficits. Arrow indicates the affected child. Full symbols indicate the individuals carrying the 17p13.3 duplication. NA indicates the individuals not available for array-CGH. B) Photographs of face and hands of the child carrying the 17p13.3 duplication. Mild facial anomalies such as thickened eyebrows, upslanting eyes, squared nasal tip, large and low-set ears. Short and stubby hands with low-set thumbs. The step mother gave consent to publish the photoghaphs of the child.

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BMC Medical Genetics

ISSN: 1471-2350

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