CHD7 mutations in patients initially diagnosed with Kallmann syndrome – the clinical overlap with CHARGE syndrome.
Jongmans, M. C. J.; van Ravenswaaij-Arts, C. M. A.; Pitteloud, N.; Ogata, T.; Sato, N.; Claahsen-van der Grinten, H. L.; van der Donk, K.; Seminara, S.; Bergman, J. E. H.; Brunner, H. G.; Crowley Jr., W. F.; Hoefsloot, L. H.; Clinical Genetics, 2009, vol. 75, issue 1, p 65, ISSN 00099163. ISBN 13990004.

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