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Pediatric Neurology|September 1, 1988
Macro cisterna magna: a marker for maldevelopment of the brain?J B Bodensteiner, C T Gay, W A Marks, et al.Clinical Genetics|December 1, 1991
An autosomal recessive form of benign familial neonatal seizuresR Schiffmann, Y Shapira, S G RyanNeurology|March 1, 1992
Spontaneous regression of optic glioma in a patient with neurofibromatosisA E Brzowski, C Bazan, J V Mumma, et al.American Journal of Medical Genetics|September 15, 1992
Proximal 7q interstitial deletion in a severely mentally retarded and mildly abnormal infantP J Gillar, C I Kaye, S G Ryan, et al.American Journal of Human Genetics|September 1, 1993
Genetic heterogeneity in benign familial neonatal convulsions: identification of a new locus on chromosome 8qT B Lewis, R J Leach, K Ward, et al.Journal of Child Neurology|May 1, 1996
Evidence of a third locus for benign familial convulsionsT B Lewis, M I Shevell, E Andermann, et al.Annals of Neurology|May 1, 1991
Benign familial neonatal convulsions: evidence for clinical and genetic heterogeneityS G Ryan, M Wiznitzer, C Hollman, et al.American Journal of Medical Genetics|April 29, 1998
Chromosome 18q paracentric inversion in a family with mental retardation and hearing lossK M Keppler-Noreuil, A J Carroll, S C Finley, et al.Endocrinology|November 1, 1988
A new highly potent parathyroid hormone antagonist: [D-Trp12,Tyr34]bPTH-(7-34)NH2M E Goldman, R L McKee, M P Caulfield, et al.Pageof 4