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Science (New York, N.Y.)|May 20, 2006
Comment on "The Brain of LB1, Homo floresiensis"R D Martin, A M Maclarnon, J L Phillips, et al.American Journal of Medical Genetics|April 1, 1986
Familial Miller-Dieker syndrome associated with pericentric inversion of chromosome 17F Greenberg, R F Stratton, L H Lockhart, et al.Neurology|October 29, 2003
Mosaic mutations of the LIS1 gene cause subcortical band heterotopiaF Sicca, A Kelemen, P Genton, et al.Neuropediatrics|April 1, 1996
Cobblestone lissencephaly with normal eyes and muscleW B Dobyns, M A Patton, R F Stratton, et al.Human Molecular Genetics|February 1, 1997
Point mutations and an intragenic deletion in LIS1, the lissencephaly causative gene in isolated lissencephaly sequence and Miller-Dieker syndromeC Lo Nigro, C S Chong, A C Smith, et al.American Journal of Medical Genetics|March 21, 1998
Complete absence or deficiency of one half of the bodyA Carranza, E Gilbert-Barness, F Madrigal, et al.American Journal of Medical Genetics|April 17, 1998
Errors of morphogenesis and developmental field theoryM L Martínez-Frías, J L Frías, J M OpitzAmerican Journal of Medical Genetics|October 1, 1984
Sensorineural deafness in the FG syndrome: report on four new casesG Neri, B Blumberg, P V Miles, et al.American Journal of Medical Genetics|December 14, 1999
Blaschkolinear malformation syndrome in complex trisomy-7 mosaicismE Magenis, M J Webb, B Spears, et al.Archives of Pathology & Laboratory Medicine|January 1, 1978
Hematological and biochemical paraneoplastic disordersH M Payan, E F Gilbert, M MattsonPageof 40