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European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|September 7, 1999
Rapid onset dystonia-parkinsonism in a 14-year-old girlD W Webb, A Broderick, A Brashear, et al.JAMA|December 15, 1993
Lissencephaly. A human brain malformation associated with deletion of the LIS1 gene located at chromosome 17p13W B Dobyns, O Reiner, R Carrozzo, et al.The American Journal of Cardiovascular Pathology|January 1, 1987
The effects of metabolic diseases on the cardiovascular systemE F GilbertTrends in Neurosciences|August 17, 2001
LIS1: from cortical malformation to essential protein of cellular dynamicsR J Leventer, C Cardoso, D H Ledbetter, et al.Human Genetics|August 1, 1988
Familial pericentric and paracentric inversions of chromosome 1D D Johnson, W B Dobyns, H Gordon, et al.American Journal of Human Genetics|August 1, 1997
Identification of a duplication of Xq28 associated with bilateral periventricular nodular heterotopiaJ M Fink, W B Dobyns, R Guerrini, et al.American Journal of Human Genetics|January 1, 1992
Microdeletions of chromosome 17p13 as a cause of isolated lissencephalyS A Ledbetter, A Kuwano, W B Dobyns, et al.Neurology|August 15, 2001
LIS1 missense mutations cause milder lissencephaly phenotypes including a child with normal IQR J Leventer, C Cardoso, D H Ledbetter, et al.Journal of Medical Genetics|May 10, 2005
Oculocerebrocutaneous syndrome: the brain malformation defines a core phenotypeU Moog, M C Jones, L M Bird, et al.Pageof 40