548 results on '"Carter, Nigel P."'
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2. Teledentistry: A global solution with local impact
3. Cost of living and access to dentistry crises: A perfect storm?
4. The Replica Dataset: A Digital Replica of Indoor Spaces
5. Mouth cancer: the challenges ahead
6. The challenges of mouth cancer awareness in a post-COVID world increasingly resistant to change
7. Supplementary Tables S1-S4 from Genome-Wide Screening of Genomic Alterations and Their Clinicopathologic Implications in Non–Small Cell Lung Cancers
8. Genetic diagnosis of developmental disorders in the DDD study: a scalable analysis of genome-wide research data
9. Generation of Paint Probes by Flow-Sorted and Microdissected Chromosomes
10. Array-CGH for the Analysis of Constitutional Genomic Rearrangements
11. Waterbodies thermal energy based systems interactions with marine environment — A review
12. Genome Sequencing and Analysis of the Tasmanian Devil and Its Transmissible Cancer
13. Generation of Paint Probes from Flow-Sorted and Microdissected Chromosomes
14. Chromosomal breaks at FRA18C: association with reduced DOK6 expression, altered oncogenic signaling and increased gastric cancer survival
15. Molecular Cytogenetics: Uses of flow sorted chromosomes, fluorescence in situ hybridisation (FISH) and digital microscopy for the analysis of genomes
16. Massive Genomic Rearrangement Acquired in a Single Catastrophic Event during Cancer Development
17. Paired-End Mapping Reveals Extensive Structural Variation in the Human Genome
18. Consensus Statement: Chromosomal Microarray Is a First-Tier Clinical Diagnostic Test for Individuals with Developmental Disabilities or Congenital Anomalies
19. Differential DNA Methylation as a Tool for Noninvasive Prenatal Diagnosis (NIPD) of X Chromosome Aneuploidies
20. Distinct Effects of Allelic NFIX Mutations on Nonsense-Mediated mRNA Decay Engender Either a Sotos-like or a Marshall-Smith Syndrome
21. Genomic and Genic Deletions of the FOX Gene Cluster on 16q24.1 and Inactivating Mutations of FOXF1 Cause Alveolar Capillary Dysplasia and Other Malformations
22. The Role of DNA Copy Number Variation in Schizophrenia
23. Sites of Differential DNA Methylation between Placenta and Peripheral Blood: Molecular Markers for Noninvasive Prenatal Diagnosis of Aneuploidies
24. Breakpoint Mapping and Array CGH in Translocations: Comparison of a Phenotypically Normal and an Abnormal Cohort
25. Fetal-specific DNA methylation ratio permits noninvasive prenatal diagnosis of trisomy 21
26. Adaptive Evolution of UGT2B17 Copy-Number Variation
27. Origins and functional impact of copy number variation in the human genome
28. Reduced TFAP2A function causes variable optic fissure closure and retinal defects and sensitizes eye development to mutations in other morphogenetic regulators
29. Avian comparative genomics: reciprocal chromosome painting between domestic chicken (Gallus gallus) and the stone curlew (Burhinus oedicnemus, Charadriiformes)—An atypical species with low diploid number
30. Adaptive evolution of UGT2B17 copy-number variation
31. Autosomal-dominant microtia linked to five tandem copies of a copy-number-variable region at chromosome 4p16
32. Spreading of mammalian DNA‐damage response factors studied by ChIP‐chip at damaged telomeres
33. Radial chromatin positioning is shaped by local gene density, not by gene expression
34. A complex rearrangement on chromosome 22 affecting both homologues; haplo-insufficiency of the Cat eye syndrome region may have no clinical relevance
35. Micro-array analyses decipher exceptional complex familial chromosomal rearrangement
36. Identification and analysis of functional elements in 1% of the human genome by the ENCODE pilot project
37. Completing the map of human genetic variation
38. Mutations in TCF4, encoding a class I basic helix-loop-helix transcription factor, are responsible for Pitt-Hopkins syndrome, a severe epileptic encephalopathy associated with autonomic dysfunction
39. Report of a female patient with mental retardation and tall stature due to a chromosomal rearrangement disrupting the OPHN1 gene on Xq12
40. Investigating chromosome organization with genomic microarrays
41. Array-CGH analysis of microsatellite-stable, near-diploid bowel cancers and comparison with other types of colorectal carcinoma
42. A novel 5q11.2 deletion detected by microarray comparative genomic hybridisation in a child referred as a case of suspected 22q11 deletion syndrome
43. Global variation in copy number in the human genome
44. High-resolution analysis of genomic copy number alterations in bladder cancer by microarray-based comparative genomic hybridization
45. Chromosome paints from single copies of chromosomes
46. Heterogeneous duplications in patients with Pelizaeus-Merzbacher disease suggest a mechanism of coupled homologous and nonhomologous recombination
47. The DNA sequence of the human X chromosome
48. Construction and integration of radiation-hybrid and cytogenetic maps of dog Chromosome X
49. Chromatin architecture of the human genome: gene-rich domains are enriched in open chromatin fibers
50. The zebrafish reference genome sequence and its relationship to the human genome
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