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1. Current Perspectives to Environment and Climate Change Vol. 2

3. ESEA Title I Linking Project. Final Report.

9. Missense mutations in the AFG3L2 proteolytic domain account for ~1.5% of European autosomal dominant cerebellar ataxias

10. Contributors

11. Spinocerebellar Ataxia Type 12

12. Huntington's Disease-like 2

13. Spinocerebellar Ataxia 12 (SCA12)

14. High frequency retrotransposition in cultured mammalian cells

18. Assessing parental utilization of the poison center: an emergency center-based survey

19. Blood lead levels in a continuity clinic population

20. CSAR: An Interactive Item Bank System for the Storage and Retrieval of Item Information.

21. Test Equating and Credentialing Examinations.

22. A Survey of Adult Reading Patterns and Library Use Patterns in Orem, Utah.

23. Item Banking: An Alternative Approach to Title I Evaluation?

24. The Effects of Test Content Match and Number of Items on the Accuracy of Trait Estimates from Tests Equated with the Three-Parameter Logistic Model.

25. Test Equating Issues in Certification and Licensure Testing.

26. Multi-Purpose Tests: A Solution to Test Proliferation.

27. Criterion-Referenced Standard-Setting in Certification and Licensure: Defining the Minimally Competent Candidate.

28. An Empirical Study of Vertical Equating Methods Using the Three-Parameter Logistic Model.

29. Two-Group Comparisons and Univariate Classification.

31. Neuropathology and Cellular Pathogenesis of Spinocerebellar Ataxia Type 12

32. Neuropathology and Cellular Pathogenesis of Spinocerebellar Ataxia Type 12

35. Huntington's Disease-like 2 (HDL2) in North America and Japan.

36. Missense mutations in the AFG3L2 proteolytic domain account for ∼1.5% of European autosomal dominant cerebellar ataxias

38. Long tandem repeats as a form of genomic copy number variation: structure and length polymorphism of a chromosome 5p repeat in control and schizophrenia populations

41. Huntington's disease-like 2 (HDL2) in North America and Japan

45. Trinucleotide repeat expansions in the junctophilin‐3 gene are not found in caucasian patients with a huntington's disease‐like phenotype

47. A repeat expansion in the gene encoding junctophilin-3 is associated with Huntington disease–like 2

49. SCA12 is a rare locus for autosomal dominant cerebellar ataxia: A study of an Indian family

50. Expansion of a novel CAG trinucleotide repeat in the 5′ region of PPP2R2B is associated with SCA12

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