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 journal › Article › peer-review

Cite this

@article{fbfbaea850264a72a3e49581482a77fc,

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

author = "C.J. Ellaway and N. Badawi and L. Raffaele and J. Christodoulou and H. Leonard",

year = "2001",

language = "English",

volume = "10",

pages = "185--188",

journal = "Clinical Dysmorphology",

issn = "0962-8827",

publisher = "Lippincott Williams & Wilkins",

}