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Fanconi anaemia complementation group B presenting as X linked VACTERL with hydrocephalus syndrome
- Correspondence to: Dr Simon Holden Department of Clinical Genetics, 7th Floor New Guy’s House, Guy’s Hospital, St Thomas Street, London SE1 9RT, UK; simon.holden{at}gstt.nhs.uk
Citation
Fanconi anaemia complementation group B presenting as X linked VACTERL with hydrocephalus syndrome
Publication history
- Received February 11, 2006
- Accepted April 17, 2006
- Revised April 13, 2006
- First published May 5, 2006.
Online issue publication
April 27, 2016
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Copyright 2006 Journal of Medical Genetics