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Immune Checkpoint Inhibition as Primary Adjuvant Therapy for an IDH1 -Mutant Anaplastic Astrocytoma in a Patient with CMMRD: A Case Report-Usage of Immune Checkpoint Inhibition in CMMRD
Current oncology (Toronto), 2021-02, Vol.28 (1), p.757-766
2021
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Referral, Genetic Counselling, and BRCA Testing in the Manitoba High-Grade Serous Ovarian Cancer Population, 2004-2019
Current oncology (Toronto), 2022-11, Vol.29 (12), p.9365-9376
2022
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Sa1185 ASCERTAINMENT OF LYNCH SYNDROME IN MANITOBA: A POPULATION-BASED STUDY
Gastroenterology (New York, N.Y. 1943), 2023-05, Vol.164 (6), p.S-318-S-318
2023
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Clinical genetics and the Hutterite population: A review of Mendelian disorders
American journal of medical genetics. Part A, 2008-04, Vol.146A (8), p.1088-1098
2008
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How Common are Uterine Doppler Abnormalities for Pregnant Patients with Elevated Maternal Serum Alpha-Fetoprotein (MS-AFP)?
Journal of obstetrics and gynaecology Canada, 2022-05, Vol.44 (5), p.625-625
2022
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Quantifying the risk of placentally-mediated complications of pregnancy after false-positive combined screens for aneuploidy
American journal of obstetrics and gynecology, 2022-01, Vol.226 (1), p.S643-S644
2022
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Tu1101: QUALITY ASSESSMENT OF A PROVINCIAL SCREENING PROGRAM FOR LYNCH SYNDROME
Gastroenterology (New York, N.Y. 1943), 2022-05, Vol.162 (7), p.S-883-S-883
2022
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Second and first trimester estimation of risk for Down syndrome: implementation and performance in the SAFER study
Prenatal diagnosis, 2010-05, Vol.30 (5), p.459-466
2010
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Referral, Genetic Counselling, and IBRCA/I Testing in the Manitoba High-Grade Serous Ovarian Cancer Population, 2004–2019
Current oncology (Toronto), 2022-11, Vol.29 (12)
2022
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Genetic Linkage of the Dehydrated Hereditary Stomatocytosis Locus to Chromosome 16 in Two Kindreds and Refinement of the Candidate Gene Region to 16q24.2 - 16qter
Blood, 2011-11, Vol.118 (21), p.3170-3170
2011
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Phenotypic Evaluation of a Family Cohort with Hemolytic Anemia
Blood, 2010-11, Vol.116 (21), p.3214-3214
2010
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large novel deletion in the APC promoter region causes gene silencing and leads to classical familial adenomatous polyposis in a Manitoba Mennonite kindred
Human genetics, 2008-12, Vol.124 (5), p.535-541
2008
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Immune Checkpoint Inhibition as Primary Adjuvant Therapy for an IDH1-Mutant Anaplastic Astrocytoma in a Patient with CMMRD: A Case Report-Usage of Immune Checkpoint Inhibition in CMMRD
Current oncology (Toronto, Ont.), 2021, Vol.28 (1), p.757-766
2021
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Molecular and clinical correlation study of Williams-Beuren syndrome: No evidence of molecular factors in the deletion region or imprinting affecting clinical outcome
American journal of medical genetics, 1999-09, Vol.86 (1), p.34-43
1999
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