학술논문
Mutations in KIF11 cause autosomal-dominant microcephaly variably associated with congenital lymphedema and chorioretinopathy
Document Type
Article
Author
Ostergaard, P.; Jeffery, S.; Simpson, M.A.; Onoufriadis, A.; Trembath, R.C.; Mendola, A.; Ghalamkarpour, A.; Vikkula, M.; Vasudevan, P.; Connell, F.C.; Van Impel, A.; Schulte-Merker, S.; Moore, A.T.; Loeys, B.L.; Van Laer, L.; Martinez-Corral, I.; Makinen, T.; Devery, S.; Leroy, J.G.; Singer, A.; Bialer, M.G.; McEntagart, M.; Brice, G.; Mansour, S.; Quarrell, O.; Mortimer, P.S.
Source
In: American Journal of Human Genetics . (American Journal of Human Genetics, 10 February 2012, 90(2):356-362)
Subject
Language
English
ISSN
00029297
15376605
15376605