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1. Exome copy number variant detection, analysis, and classification in a large cohort of families with undiagnosed rare genetic disease.

2. A CCG expansion in ABCD3 causes oculopharyngodistal myopathy in individuals of European ancestry

3. Author Correction: A CCG expansion in ABCD3 causes oculopharyngodistal myopathy in individuals of European ancestry

4. A common flanking variant is associated with enhanced stability of the FGF14-SCA27B repeat locus

5. The GENESIS database and tools: A decade of discovery in Mendelian genomics

7. Loss of function variants in DNAJB4 cause a myopathy with early respiratory failure

8. A novel phenotype of AChR-deficiency syndrome with predominant facial and distal weakness resulting from the inclusion of an evolutionary alternatively-spliced exon in CHRNA1

11. A deep intronic variant in MME causes autosomal recessive Charcot–Marie–Tooth neuropathy through aberrant splicing

12. Genome Sequencing for Diagnosing Rare Diseases

13. Generation of two iPSC lines from adult central core disease patients with dominant missense variants in the RYR1 gene

14. Biallelic variants in ARHGAP19 cause a motor-predominant neuropathy with asymmetry and conduction slowing

17. An Update on Reported Variants in the Skeletal Muscle α‐Actin (ACTA1) Gene.

18. Loss- of- function variants in JPH1 cause congenital myopathy with prominent facial and ocular involvement.

19. De novo variants in ATXN7L3 lead to developmental delay, hypotonia and distinctive facial features.

21. Pathogenic TNNI1 variants disrupt sarcomere contractility resulting in hypo- and hypercontractile muscle disease

22. Generation of two iPSC lines from patients with inherited central core disease and concurrent malignant hyperthermia caused by dominant missense variants in the RYR1 gene

23. Detecting missed diagnoses of spinal muscular atrophy in genome, exome, and panel sequencing datasets

24. A splice-altering homozygous variant in COX18 causes severe sensory-motor neuropathy with oculofacial apraxia

27. Recessive MYH7-related myopathy in two families

29. Role of the repeat expansion size in predicting age of onset and severity in RFC1 disease.

30. A deep intronic FGF14 GAA repeat expansion causes late-onset cerebellar ataxia

31. Generation of two induced pluripotent stem cell lines from a 33-year-old central core disease patient with a heterozygous dominant c.14145_14156delCTACTGGGACA (p.Asn4715_Asp4718del) deletion in the RYR1 gene

33. Biallelic variants inHMGCS1are a novel cause of rare rigid spine syndrome

34. Exome copy number variant detection, analysis and classification in a large cohort of families with undiagnosed rare genetic disease

37. NEMF mutations that impair ribosome-associated quality control are associated with neuromuscular disease

38. Author Correction: NEMF mutations that impair ribosome-associated quality control are associated with neuromuscular disease

40. Nebulin nemaline myopathy recapitulated in a compound heterozygous mouse model with both a missense and a nonsense mutation in Neb

41. The genetic landscape of axonal neuropathies in the middle-aged and elderly: Focus on MME

42. Ablation of the carboxy-terminal end of MAMDC2 causes a distinct muscular dystrophy

43. Dynamic regulation of inter-organelle communication by ubiquitylation controls skeletal muscle development and disease onset

44. A common flanking variant is associated with enhanced meiotic stability of theFGF14-SCA27B locus

45. CAV3 mutations causing exercise intolerance, myalgia and rhabdomyolysis: Expanding the phenotypic spectrum of caveolinopathies

46. Myoglobinopathy is an adult-onset autosomal dominant myopathy with characteristic sarcoplasmic inclusions

47. A KLHL40 3' UTR splice-altering variant causes milder NEM8, an under-appreciated disease mechanism

48. Ablation of the carboxy-terminal end of MAMDC2 causes a distinct muscular dystrophy

49. Author response: Dynamic regulation of inter-organelle communication by ubiquitylation controls skeletal muscle development and disease onset

50. Expanding the phenotype of DNMT3A as a cause a congenital myopathy with rhabdomyolysis

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