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1. Immunogenetics associated with severe coccidioidomycosis

2. Endocannabinoid dysfunction in neurological disease: neuro-ocular DAGLA-related syndrome (NODRS)

3. A novel DPH5-related diphthamide-deficiency syndrome causing embryonic lethality or profound neurodevelopmental disorder

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

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

9. De novo variants in DENND5B cause a neurodevelopmental disorder

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

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

13. Natural history study of patients with familial platelet disorder with associated myeloid malignancy

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

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

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

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

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

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

23. De novo variants in DENND5B cause a neurodevelopmental disorder

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

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

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

27. Genomic Landscape of Patients with Germline RUNX1 Variants and Familial Platelet Disorder with Myeloid Malignancy

29. Hypomorphic caspase activation and recruitment domain 11 (CARD11) mutations associated with diverse immunologic phenotypes with or without atopic disease

30. Natural history of autoimmune lymphoproliferative syndrome associated with FAS gene mutations

31. Bone Density and Fractures in Autosomal Dominant Hyper IgE Syndrome

32. Early intervention in STAT3 dominant negative disease

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

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

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

37. Intermediate phenotypes in patients with autosomal dominant hyper-IgE syndrome caused by somatic mosaicism

39. GATA2 at 10: Emergence of Genotype-Phenotye correlations

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

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

45. Genomic Landscape of Patients with GermlineRUNX1Variants and Familial Platelet Disorder with Myeloid Malignancy

46. A novel GATA2distal enhancer mutation results in MonoMAC syndrome in 2 second cousins

47. Clinical exome sequencing of 1000 families with complex immune phenotypes: Toward comprehensive genomic evaluations

48. Missense and truncating variants in CHD5 in a dominant neurodevelopmental disorder with intellectual disability, behavioral disturbances, and epilepsy

50. Correction to: An autosomal dominant neurological disorder caused by de novo variants in FAR1 resulting in uncontrolled synthesis of ether lipids

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