Search

Your search keyword '"Newlin, Anna"' showing total 41 results

Search Constraints

Start Over You searched for: Author "Newlin, Anna" Remove constraint Author: "Newlin, Anna"
41 results on '"Newlin, Anna"'

Search Results

1. A prospective prostate cancer screening programme for men with pathogenic variants in mismatch repair genes (IMPACT): initial results from an international prospective study

7. A prospective prostate cancer screening programme for men with pathogenic variants in mismatch repair genes (IMPACT): initial results from an international prospective study

11. List of Contributors

14. Psychosocial impact of undergoing prostate cancer screening for men with BRCA1 or BRCA2 mutations

15. Psychosocial impact of undergoing prostate cancer screening for men with BRCA1 or BRCA2 mutations

16. Prostate-specific antigen velocity in a prospective prostate cancer screening study of men with genetic predisposition

17. Postmortem Somatic Sequencing of Tumors From Patients With Suspected Lynch Syndrome Has Clinical Utility for Surviving Relatives

18. Erratum: Prostate-specific antigen velocity in a prospective prostate cancer screening study of men with genetic predisposition

19. Point Mutations in Exon 1B of APC Reveal Gastric Adenocarcinoma and Proximal Polyposis of the Stomach as a Familial Adenomatous Polyposis Variant

20. Targeted Prostate Cancer Screening in BRCA1 and BRCA2 Mutation Carriers: Results from the Initial Screening Round of the IMPACT Study

24. Human TUBB3 Mutations Perturb Microtubule Dynamics, Kinesin Interactions, and Axon Guidance

25. Psychological impact of recall in high-risk breast MRI screening

29. Heterozygous mutations of the kinesin KIF21A in congenital fibrosis of the extraocular muscles type 1 (CFEOM1)

30. Craniofacial Syndromes and Malformations.

38. List of Contributors

39. Prostate-specific antigen velocity in a prospective prostate cancer screening study of men with genetic predisposition.

40. Psychological impact of recall in high-risk breast MRI screening.

41. Characterization and prevalence of PITX2 microdeletions and mutations in Axenfeld-Rieger malformations.

Catalog

Books, media, physical & digital resources