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A case of multiple congenital anomalies in association with Rett syndrome confirmed by MECP2 mutation screening.

Pubmed ID: 
11446411
Year: 
2001
Month: 
Jul
Volume: 
10
Issue: 
3
Citation: 
Ellaway CJ, Badawi N, Raffaele L, Christodoulou J, Leonard H. A case of multiple congenital anomalies in association with Rett syndrome confirmed by MECP2 mutation screening. Clinical dysmorphology 10 (3) : 185 - 8(2001) PubMed