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1. Why Did We Do This? Collective Faculty Motivations to Engage in Accreditation Work

2. Preservice Teachers' Perceptions of Their Knowledge of and Confidence in Using High-Leverage Practices

3. The Undiagnosed Diseases Network: Characteristics of solvable applicants and diagnostic suggestions for nonaccepted ones

4. Dominant missense variants in SREBF2 are associated with complex dermatological, neurological, and skeletal abnormalities

5. Loss of function of FAM177A1, a Golgi complex localized protein, causes a novel neurodevelopmental disorder

6. Cohort Expansion and Genotype-Phenotype Analysis of RAB11A-Associated Neurodevelopmental Disorder

7. Loss-of-function in RBBP5 results in a syndromic neurodevelopmental disorder associated with microcephaly

8. Homelessness in Children's Literature: A Path to Opening Additional Mirrors, Windows and Sliding Glass Doors

9. De novo missense variants in phosphatidylinositol kinase PIP5KIγ underlie a neurodevelopmental syndrome associated with altered phosphoinositide signaling

10. Exome and genome sequencing in a heterogeneous population of patients with rare disease: Identifying predictors of a diagnosis

11. De novo variants in DENND5B cause a neurodevelopmental disorder

12. Biallelic CRELD1 variants cause a multisystem syndrome, including neurodevelopmental phenotypes, cardiac dysrhythmias, and frequent infections

14. A syndromic neurodevelopmental disorder caused by rare variants in PPFIA3

15. Genomics Research with Undiagnosed Children: Ethical Challenges at the Boundaries of Research and Clinical Care

17. Biallelic variants in ribonuclease inhibitor (RNH1), an inflammasome modulator, are associated with a distinctive subtype of acute, necrotizing encephalopathy

18. HNRNPC haploinsufficiency affects alternative splicing of intellectual disability-associated genes and causes a neurodevelopmental disorder

19. De novo variants in MRTFB have gain-of-function activity in Drosophila and are associated with a novel neurodevelopmental phenotype with dysmorphic features

20. Bi-allelic variants in INTS11 are associated with a complex neurological disorder

21. De Novo Variants in the ATPase Module of MORC2 Cause a Neurodevelopmental Disorder with Growth Retardation and Variable Craniofacial Dysmorphism

22. A concurrent dual analysis of genomic data augments diagnoses: Experiences of 2 clinical sites in the Undiagnosed Diseases Network

24. Supporting Effective Guided Reading Instruction for All Students

25. Exome and genome sequencing in a heterogeneous population of patients with rare disease: Identifying predictors of a diagnosis

26. C. elegans as a model for inter-individual variation in metabolism

31. Connecting with Your Toughest Kids: Structuring Teacher-Student Relationship Interventions with MTSS.

35. De novo variants in DENND5B cause a neurodevelopmental disorder

36. The Future of Forceps Delivery in Canada

37. Phenotypic expansion of CACNA1C-associated disorders to include isolated neurological manifestations

38. Heterozygous loss-of-function variants significantly expand the phenotypes associated with loss of GDF11

39. PIGG variant pathogenicity assessment reveals characteristic features within 19 families

40. Torpor use in the wild by one of the world's largest bats.

42. Partial Loss of USP9X Function Leads to a Male Neurodevelopmental and Behavioral Disorder Converging on Transforming Growth Factor β Signaling

45. A syndromic neurodevelopmental disorder caused by rare variants in PPFIA3

46. De novo missense variants in phosphatidylinositol kinase PIP5KIγ underlie a neurodevelopmental syndrome associated with altered phosphoinositide signaling

49. Biallelic CRELD1 variants cause a multisystem syndrome including neurodevelopmental phenotypes, cardiac dysrhythmias, and frequent infections.

50. Sex differences in fetal Doppler parameters during gestation

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