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10. Neutron Capture on the s -Process Branching Point Tm 171

12. Motor system abnormalities in hereditary spastic paraparesis type 4 (SPG4) depend on the type of mutation in the spastin gene

13. Polycrystalline homogenization accounting for grain size effects through slip bands in FCC metals and alloys

14. Prediction of grain boundary micro-crack initiation during cyclic deformation

17. Fourth meeting of the European Neurological Society 25–29 June 1994 Barcelona, Spain: Abstracts of Symposia and free communications

20. Homogénéisation du comportement polycristallin : considérer la plasticité à l'échelle des grains ou des bandes de glissement ?

21. Efficacy of exome-targeted capture sequencing to detect mutations in known cerebellar ataxia genes

22. Prediction of intergranular micro-cracks initiation induced by the impingement of persistent slip bands on grain boundaries

24. Prediction of grain boundary stress fields induced by the impingement of persistent slip bands

25. Prediction des champs de contraintes et dedeformations induits par l'impact de bandes deglissement persistantes aux joints de grains

30. Genetic and functional analyses demonstrate a role for abnormal glycinergic signaling in autism

31. The EUROGEM map of human chromosome 20

36. 1050 DELIRIUM RECOGNITION AND MANAGEMENT IN AN INPATIENT REHABILITATION UNIT.

37. Phenotype of autosomal dominant spastic paraplegia linked to chromosome 2

42. The use marker alleles for the introgression of linked quantitative alleles.

45. Mutation analysis of the spastin gene (SPG4) in patients with hereditary spastic paraparesis

47. Quality assessment of whole genome mapping data in the refined familial spastic paraplegia interval on chromosome 14q.

48. Mapping of a complicated familial spastic paraplegia to locus SPG4 on chromosome 2p

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