46 results on '"Sutherland Joanne"'
Search Results
2. Correction: Gene therapy: perspectives from young adults with Leber’s congenital amaurosis
3. Improved diagnostic yield compared with targeted gene sequencing panels suggests a role for whole-genome sequencing as a first-tier genetic test
4. Building an Academic Nation through Social Networks: Black Immigrant Men in Community Colleges
5. Expanding Access Through Doctoral Education: Perspectives from Two Participants of the Sisters of the Academy Research Boot Camp
6. Management and outcome of unilateral retinoblastoma
7. Human Ribosomal RNA Genes: Orientation of the Tandem Array and Conservation of the 5$^{\prime}$ End
8. Gene therapy: perspectives from young adults with Leber’s congenital amaurosis
9. OTX2 mutations cause autosomal dominant pattern dystrophy of the retinal pigment epithelium
10. The Ocular Genetics Program: multidisciplinary care of patients with ocular genetic eye disease
11. Ocular Manifestations of Chromosomal Abnormalities
12. Genetic Counseling for Genetic Eye Disorders
13. Exome sequencing identifies NMNAT1 mutations as a cause of Leber congenital amaurosis
14. Utility of molecular testing for related retinal dystrophies
15. Advantages and disadvantages of molecular testing in ophthalmology
16. Counseling and screening for cystic fibrosis in patients with congenital bilateral absence of the vas deferens: Patient perceptions
17. Frequency of somatic and germ-line mosaicism in retinoblastoma: implications for genetic counseling
18. Phenotypic heterogeneity of CYP1B1: mutations in a patient with Petersʼ anomaly
19. Sensitive and Efficient Detection of RB1 Gene Mutations Enhances Care for Families with Retinoblastoma
20. Molecular characterisation of congenital glaucoma in a consanguineous Canadian community: a step towards preventing glaucoma related blindness
21. Eight previously unidentified mutations found in the OA1 ocular albinism gene
22. Evaluation of minimally invasive blood pressure telemetry devices in conscious Beagle dogs
23. Validation of the minimally invasive blood pressure telemetry technique for use in repeat-dose toxicology studies
24. Genetic counseling and genetic testing in ophthalmology
25. 005: A 20-year review of the management and outcome of unilateral retinoblastoma
26. Psychosocial Adjustment to Visual Loss in Patients with Retinitis Pigmentosa
27. Eight previously unidentified mutations found in the OA1ocular albinism gene
28. Unique insertional translocation in a childhood Wilms' tumor survivor detected when his daughter developed bilateral retinoblastoma
29. Mutational analysis of the OA1 gene in ocular albinism
30. Mutation analysis of the tyrosinase gene in oculocutaneous albinism
31. Impact of carrier status determination for Duchenne/Becker muscular dystrophy by computer-assisted laser densitometry
32. Improving access to services in neuro-developmental disability: proceedings of a national meeting to advance community capacity.
33. Isolation and characterization of a major tandem repeat family from the human X chromosome.
34. A novel mutation in the Norrie disease gene predicted to disrupt the cystine knot growth factor motif.
35. An orientation to researching leadership for learning.
36. Reclaiming Rhetorical Women in the Rhetorical Tradition.
37. Teaching About Social Justice Issues in Physical Education
38. The Medical Directory 2015
39. Turner Classic Movies Presents Leonard Maltin's Classic Movie Guide : From the Silent Era Through 1965: Third Edition
40. The Medical Directory 2014, 168th Edition
41. Holly Would Dream
42. United Kingdom : Magic circle retail finance lawyer returns to Eversheds Sutherland
43. Magic circle retail finance lawyer returns to Eversheds Sutherland
44. Trollope and the Magazines : Gendered Issues in Mid-Victorian Britain
45. Letters: People living near Heathrow want speedy airport expansion there; Back Heathrow and 2,000 London residents voice their support for expansion at Heathrow
46. OBITUARIES
Catalog
Books, media, physical & digital resources
Discovery Service for Jio Institute Digital Library
For full access to our library's resources, please sign in.