CHD7 mutations in patients initially diagnosed with Kallmann syndrome - the clinical overlap with CHARGE syndrome

M. C. J. Jongmans*, C. M. A. van Ravenswaaij-Arts, N. Pitteloud, T. Ogata, N. Sato, H. L. Claahsen-van der Grinten, K. van der Donk, S. Seminara, J. E. H. Bergman, H. G. Brunner, W. F. Crowley, L. H. Hoefsloot

*Corresponding author for this work

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Medicine and Dentistry

Neuroscience

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Biochemistry, Genetics and Molecular Biology