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2. 3D genomic mapping reveals multifocality of human pancreatic precancers

3. PanIN or IPMN? Redefining Lesion Size in 3 Dimensions

6. Progression and Resolution of Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) Infection in Golden Syrian Hamsters

7. CNVs cause autosomal recessive genetic diseases with or without involvement of SNV/indels

10. Intraductal Papillary Mucinous Neoplasms Arise From Multiple Independent Clones, Each With Distinct Mutations

11. Misattributed parentage as an unanticipated finding during exome/genome sequencing: current clinical laboratory practices and an opportunity for standardization

13. Three-dimensional assessments are necessary to determine the true, spatially-resolved composition of tissues

15. Surgical Protocol for Partial Heart Transplantation in Growing Piglets

19. Copy number variant and runs of homozygosity detection by microarrays enabled more precise molecular diagnoses in 11,020 clinical exome cases

21. Three-dimensional genomic mapping of human pancreatic tissue reveals striking multifocality and genetic heterogeneity in precancerous lesions

23. Clinical exome sequencing for fetuses with ultrasound abnormalities and a suspected Mendelian disorder

30. Progression and Resolution of Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) Infection in Golden Syrian Hamsters

32. Molecular Findings Among Patients Referred for Clinical Whole-Exome Sequencing

33. Sex Differences in Lung Imaging and SARS-CoV-2 Antibody Responses in a COVID-19 Golden Syrian Hamster Model

34. Clinical Whole-Exome Sequencing for the Diagnosis of Mendelian Disorders

35. In situ characterization of the 3D microanatomy of the pancreas and pancreatic cancer at single cell resolution

36. Multiregion whole-exome sequencing of intraductal papillary mucinous neoplasms reveals frequent somatic KLF4 mutations predominantly in low-grade regions

37. Intraparenchymal metastases as a cause for local recurrence of pancreatic cancer.

38. Platelet-endothelial associations may promote cytomegalovirus replication in the salivary gland in mice

39. Reanalysis of Clinical Exome Sequencing Data

40. Biallelic Variants in OTUD6B Cause an Intellectual Disability Syndrome Associated with Seizures and Dysmorphic Features

41. Multiregion whole-exome sequencing of intraductal papillary mucinous neoplasms reveals frequent somatic KLF4 mutations predominantly in low-grade regions.

42. Additional file 1: of Clinical exome sequencing for fetuses with ultrasound abnormalities and a suspected Mendelian disorder

43. Bi-allelic Mutations in PKD1L1 Are Associated with Laterality Defects in Humans

44. De Novo Truncating Variants in SON Cause Intellectual Disability, Congenital Malformations, and Failure to Thrive

45. Platelet-endothelial associations may promote cytomegalovirus replication in the salivary gland in mice.

46. Biallelic Variants In Otud6B Cause An Intellectual Disability Syndrome Associated With Seizures And Dysmorphic Features

47. Two de novo novel mutations in one SHANK3 allele in a patient with autism and moderate intellectual disability

48. Use of Exome Sequencing for Infants in Intensive Care Units

49. Biallelic Variants in OTUD6B Cause an Intellectual Disability Syndrome Associated with Seizures and Dysmorphic Features

50. Multiregion whole-exome sequencing of intraductal papillary mucinous neoplasms reveals frequent somatic KLF4mutations predominantly in low-grade regions

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