CHD7 mutations in patients initially diagnosed with Kallmann syndrome--the clinical overlap with CHARGE syndrome (Q24595634)
scientific article
Language:
(P31) (Q13442814)
(P50) (Q57595795)
(Q57419973)
(Q106489987)
(Q30116265)
(P304) 65-71
(P407) (Q1860)
(P433) 1
(P478) 75
(P577) Monday, November 17, 2008
(P921) (Q181600)
(Q1023604)
(P1433) (Q5133760)
(P1476) "CHD7 mutations in patients initially diagnosed with Kallmann syndrome--the clinical overlap with CHARGE syndrome" (language: en)
(P2093) M C J Jongmans
C M A van Ravenswaaij-Arts
N Pitteloud
N Sato
H L Claahsen-van der Grinten
K van der Donk
H G Brunner
L H Hoefsloot
(P2860) (Q24297162)
(Q21092497)
(Q24540535)
(Q24322458)
(Q24300737)
(Q24311797)
(Q28118633)
(Q28279734)
(Q28260797)
(Q37012242)
(Q30442563)
(Q36824101)
(Q34568239)
(Q51787194)
(Q46609233)
(Q48852845)
(Q47998798)
(Q50336618)
(Q50336641)
(Q52165617)
other details
description scientific article

External Links