We report on a 2-year-old child with psychomotor retardation, facial and urogenital anomalies. His chromosome constitution was 4 6 m , de1(6)(q13q15). This case further contributes to the karyotype-phenotype correlation of proximal deletion 6q syndromes.
Interstitial deletion of 13q associated with polymicrogyria
โ Scribed by Jillene M. Kogan; John C. Egelhoff; Howard M. Saal
- Publisher
- John Wiley and Sons
- Year
- 2008
- Tongue
- English
- Weight
- 234 KB
- Volume
- 146A
- Category
- Article
- ISSN
- 1552-4825
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