Suchergebnisse - "Jasperson, Kory"

PubPharm (103)

1

Risk assessment and genetic counseling for Lynch syndrome - Practice resource of the National Society of Genetic Counselors and the Collaborative Group of the Americas on Inherited Gastrointestinal Cancer

enthalten in: Journal of genetic counseling | 2022

von Holter, S. | Hall, M. | Hampel, H. | +9

2

Diagnostic criteria for constitutional mismatch repair deficiency (CMMRD) : recommendations from the international consensus working group

enthalten in: Journal of medical genetics | 2022

von Aronson, M. | Colas, C. | Shuen, A. | +11

3

Universal Germline Panel Testing for Individuals With Pheochromocytoma and Paraganglioma Produces High Diagnostic Yield

enthalten in: The Journal of clinical endocrinology and metabolism | 2022

von Horton, C. | LaDuca, H. | Deckman, A. | +7

4

Risk assessment and genetic counseling for Lynch syndrome – Practice resource of the National Society of Genetic Counselors and the Collaborative Group of the Americas on Inherited Gastrointestinal Cancer

enthalten in: Journal of Genetic Counseling | 2022

von Holter, S. | Hall, M. | Hampel, H. | +9

5

An alternative approach to establishing unbiased colorectal cancer risk estimation in Lynch syndrome

enthalten in: Genetics in medicine : official journal of the American College of Medical Genetics | 2019

von Suerink, M. | Rodríguez-Girondo, M. | van der Klift, H. | +36

6

Prevalence of Germline Mutations in Polyposis and Colorectal Cancer-Associated Genes in Patients With Multiple Colorectal Polyps

enthalten in: Clinical gastroenterology and hepatology : the official clinical practice journal of the American Gastroenterological Association | 2019

von Stanich, P. | Pearlman, R. | Hinton, A. | +4

CommentIn: Clin Gastroenterol Hepatol. 2019 Sep;17(10):1942-1944. - PMID 30876960

7

Monoallelic MUTYH carrier status is not associated with increased breast cancer risk in a multigene panel cohort

enthalten in: Familial cancer | 2019

von Fulk, K. | LaDuca, H. | Black, M. | +5

8

Comprehensive Paired Tumor/Germline Testing for Lynch Syndrome : Bringing Resolution to the Diagnostic Process

enthalten in: Journal of clinical oncology : official journal of the American Society of Clinical Oncology | 2019

von Salvador, M. | Truelson, M. | Mason, C. | +18

9

Delineating a new feature of constitutional mismatch repair deficiency (CMMRD) syndrome : breast cancer

enthalten in: Familial cancer | 2019

von Bush, L. | Aronson, M. | Tabori, U. | +3

10

Monoallelic MUTYH carrier status is not associated with increased breast cancer risk in a multigene panel cohort

enthalten in: Familial cancer | 2018

von Fulk, K. | LaDuca, H. | Black, M. | +5

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