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Journal of Medical Genetics|December 1, 1998
Classical lissencephaly syndromes: does the face reflect the brain?J E Allanson, D H Ledbetter, W B DobynsJAMA|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.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.Trends 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|January 1, 1984
New chromosomal syndrome: Miller-Dieker syndrome and monosomy 17p13R F Stratton, W B Dobyns, S D Airhart, et al.American Journal of Human Genetics|March 1, 1991
Clinical and molecular diagnosis of Miller-Dieker syndromeW B Dobyns, C J Curry, H E Hoyme, et al.Molecular Medicine Today|June 22, 2000
Lissencephaly and subcortical band heterotopia: molecular basis and diagnosisR J Leventer, D T Pilz, N Matsumoto, et al.American Journal of Human Genetics|October 1, 1991
Detection of deletions and cryptic translocations in Miller-Dieker syndrome by in situ hybridizationA Kuwano, S A Ledbetter, W B Dobyns, et al.Neurology|July 1, 1992
Causal heterogeneity in isolated lissencephalyW B Dobyns, E R Elias, A C Newlin, et al.Pageof 36