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Human Mutation|January 1, 1997
Multiple de novo MPZ (P0) point mutations in a sporadic Dejerine-Sottas caseL E Warner, M Shohat, Z Shorer, et al.Journal of Child Neurology|May 26, 1999
Periventricular brain heterotopias in a child with adrenocortical insufficiency, achalasia, alacrima, and neurologic abnormalities (Allgrove syndrome)A Zeharia, A Shuper, M Mimouni, et al.American Journal of Medical Genetics|June 1, 1989
Brachyolmia: radiographic and genetic evidence of heterogeneityM Shohat, R Lachman, H E Gruber, et al.American Journal of Medical Genetics|September 15, 1992
Twin studies in familial Mediterranean feverM Shohat, A Livneh, D Zemer, et al.Genetic Epidemiology|January 1, 1992
Two-locus mitochondrial and nuclear gene models for mitochondrial disordersX Bu, H Y Yang, M Shohat, et al.Andrologia|September 1, 1996
A new method for isolation of human antisperm antibodiesM Shohat, B Hardy, S Mannheimer, et al.Archives of Disease in Childhood|February 1, 1989
Transient tachypnoea of the newborn and asthmaM Shohat, G Levy, I Levy, et al.European Journal of Pediatrics|April 1, 1989
Recurrent ascites in an infant with perinatally acquired cytomegalovirus infectionI Levy, M Shohat, Y Levy, et al.AJNR. American Journal of Neuroradiology|November 1, 1988
CT of the temporal bone in achondroplasiaS R Cobb, M Shohat, C M Mehringer, et al.Israel Journal of Medical Sciences|August 1, 1994
Further mapping of the properdin deficiency gene in a Tunisian Jewish family--evidence for genetic homogeneityS Ash, C Johnson, M Shohat, et al.Pageof 28