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

C.J. Ellaway, N. Badawi, L. Raffaele, J. Christodoulou, H. Leonard

Research output: Contribution to journalArticle

8 Citations (Scopus)
Original languageEnglish
Pages (from-to)185-188
JournalClinical Dysmorphology
Volume10
Publication statusPublished - 2001

Cite this

Ellaway, C. J., Badawi, N., Raffaele, L., Christodoulou, J., & Leonard, H. (2001). A case of multiple congenital anomalies in association with Rett syndrome confirmed by MECP2 mutation screening. Clinical Dysmorphology, 10, 185-188.