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Description In situ hybridization. 18p (green) and 18q (red) with subtelomeric probes showing 18p deletion in the patient with De Grouchy syndrome type I (deletion 18p)
Date
Source Maranda B, Lemieux N, Lemyre E. Familial deletion 18p syndrome: case report. BMC Medical Genetics. 60, 7. 2006. PMID 16842614.
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16 September 2007

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current16:01, 16 September 2007Thumbnail for version as of 16:01, 16 September 20071,200 × 1,180 (161 KB)Filip em{{Information |Description=In situ hybridization. 18p (green) and 18q (red) with subtelomeric probes showing 18p deletion in the patient with De Grouchy syndrome type I (deletion 18p) |Source=Maranda B, Lemieux N, Lemyre E. Familial deletion 18p syndrome:
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