M. Mork

发表

Patients with unexplained mismatch repair deficiency are interested in updated genetic testing

B. Stevens, E. Vilar, S. Noblin, 2020, Hereditary cancer in clinical practice.

Somatic mismatch repair testing in evaluation of Lynch syndrome: The gap between preferred and current practices

E. Vilar, S. Noblin, M. Mork, 2020, Journal of genetic counseling.

Genetic counselor approaches to BRCA1/2 direct‐to‐consumer genetic testing results

B. Arun, M. Mork, A. Woodson, 2021, Journal of genetic counseling.

Influence of genetic counselor medical history on specialty and psychosocial practice in North America

C. Singletary, P. McCarthy Veach, Lauren Murphy, 2021, Journal of genetic counseling.

Evaluation of Patients and Families With Concern for Predispositions to Hematologic Malignancies Within the Hereditary Hematologic Malignancy Clinic (HHMC).

J. Orange, K. Bhalla, G. Garcia-Manero, 2016, Clinical lymphoma, myeloma & leukemia.

NFB-06. TREATMENT CHALLENGES IN PEDIATRIC GLIOBLASTOMA MULTIFORME WITH CONCURRENT SOMATIC AND GERMLINE NF1 MUTATIONS WITH GERMLINE MISMATCH REPAIR MUTATIONS: TWO UNIQUE CASES

S. Khatua, G. Fuller, S. Gupta, 2020, Neuro-Oncology.

Is it all Lynch Syndrome? An assessment of family history in individuals with mismatch repair deficient tumors

R. Broaddus, K. Lu, B. Fellman, 2014, Genetics in Medicine.

Perceptions of provider’s epistemic authority in response to variant of uncertain significance‐related recommendations

B. Arun, R. Volk, Sukh Makhnoon, 2020, Journal of genetic counseling.

Frameshift mutational target gene analysis identifies similarities and differences in constitutional mismatch repair‐deficiency and Lynch syndrome

M. Linnebacher, E. Vilar, F. Prall, 2017, Molecular carcinogenesis.