CHD7 mutations in patients initially diagnosed with Kallmann syndrome – the clinical overlap with CHARGE syndrome
Article first published online: 19 NOV 2008
© 2008 The Authors Journal compilation © 2008 Blackwell Munksgaard
Volume 75, Issue 1, pages 65–71, January 2009
How to Cite
Jongmans, M., Van Ravenswaaij-Arts, C., Pitteloud, N., Ogata, T., Sato, N., Claahsen-van der Grinten, H., Van Der Donk, K., Seminara, S., Bergman, J., Brunner, H., Crowley, W. and Hoefsloot, L. (2009), CHD7 mutations in patients initially diagnosed with Kallmann syndrome – the clinical overlap with CHARGE syndrome. Clinical Genetics, 75: 65–71. doi: 10.1111/j.1399-0004.2008.01107.x
- Issue published online: 31 DEC 2008
- Article first published online: 19 NOV 2008
- Received 4 June 2008, revised and accepted for publication 27 August 2008
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