CHD7 mutations in patients initially diagnosed with Kallmann syndrome--the clinical overlap with CHARGE syndrome.
Jongmans MC; van Ravenswaaij-Arts CM; Pitteloud N; Ogata T; Sato N; Claahsen-van der Grinten HL; van der Donk K; Seminara S; Bergman JE; Brunner HG; Crowley WF Jr; Hoefsloot LH; Clinical Genetics, 2009, vol. 75, issue 1, p 65, ISSN 13990004. ISBN 13990004.

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