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2. Strand-resolved mutagenicity of DNA damage and repair

3. A Phenomenological Qualitative Study of Low Teacher Retention and Morale in a Rural Poverty-Stricken School

6. The Impact of the Cooperative Mentorship Model on Faculty Preparedness to Develop Online Courses

7. The Differential Translation Capabilities of the Human DHFR2 Gene Indicates a Developmental and Tissue-Specific Endogenous Protein of Low Abundance

8. Virginia Gordon as Servant Leader

10. Observed Social Emotional Behavior at 22 Months Predicts a Later ASD Diagnosis in High-Risk Siblings

14. Advances in Cardiovascular Health in Women over the Past Decade: Guideline Recommendations for Practice

15. Observed Social Emotional Behavior at 22 Months Predicts a Later ASD Diagnosis in High-Risk Siblings

20. Creation of Spatial Mental Models with Figural Stimuli:Validation of the Emoji-based Spatial Integration Task

21. Resistance to Temptation in Toddlers at Genetic Risk for Autism Spectrum Disorder

22. Parents' Use of Internal State Language with Toddlers at High and Low Genetic Risk for Autism Spectrum Disorder

23. Information Search with Depleting and Non-Depleting Resources

24. Utilizing Molecular Epidemiology and Citizen Science for the Surveillance of Lagoviruses in Australia

27. The Australian National Rabbit Database : 50 yr of population monitoring of an invasive species

29. Sex-dimorphic genetic effects and novel loci for fasting glucose and insulin variability

31. Genome-wide association analysis identifies six new loci associated with forced vital capacity

35. SEAMLESS

38. Spellbound

39. Developmental Changes in Empathic Concern and Self-Understanding in Toddlers at Genetic Risk for Autism Spectrum Disorder

40. Self-Care Activation, Social Support, and Self-Care Behaviors among Women Living with Heart Failure

41. Parents' Use of Internal State Language with Toddlers at High and Low Genetic Risk for Autism Spectrum Disorder

44. Analyses of LMNA-negative juvenile progeroid cases confirms biallelic POLR3A mutations in Wiedemann–Rautenstrauch-like syndrome and expands the phenotypic spectrum of PYCR1 mutations

46. Genome-wide association study of age-related macular degeneration identifies associated variants in the TNXB–FKBPL–NOTCH4 region of chromosome 6p21.3

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