subject area of
- A Practical Guide to the Management of the Fetus and Newborn With Hemophilia Academic Article
- A qualitative study of women and partners from Lebanon and Quebec regarding an expanded scope of noninvasive prenatal testing Academic Article
- A unique BRCA1 mutation identified in Mongolia Academic Article
- Age at clinical onset and at ultrasonographic detection of adult polycystic kidney disease: Data for genetic counselling Academic Article
- Alpha-thalassaemia and population health in Southeast Asia Academic Article
- Breast and ovarian cancer risk perception after prophylactic salpingo-oophorectomy due to an inherited mutation in theBRCA1orBRCA2gene Academic Article
- Cancer prevention and screening in a BRCA2-positive male to female transgender patient Academic Article
- Clinical genetics provider real-time workflow study Academic Article
- Coinheritance of α-thalassemia-1 and hemoglobin E/β0-thalassemia: Practical implications for neonatal screening and genetic counseling Academic Article
- Cross-cultural perspectives on decision making regarding noninvasive prenatal testing: A comparative study of Lebanon and Quebec Academic Article
- Data sharing as a national quality improvement program: reporting on BRCA1 and BRCA2 variant-interpretation comparisons through the Canadian Open Genetics Repository (COGR) Academic Article
- Decision Analysis of Prenatal Testing for Chromosomal Disorders: What Do the Preferences of Pregnant Women Tell Us? Academic Article
- Delivery of molecular genetic services within a health care system: time analysis of the clinical workload. The Molecular Genetic Study Group. Academic Article
- Development and Pilot Evaluation of Novel Genetic Educational Materials Designed for an Underserved Patient Population Academic Article
- Double heterozygosity for germline mutations in BRCA1 and p53 in a woman with early onset breast cancer Academic Article
- Factors That Predict Risk of Thrombosis in Relatives of Patients With Unprovoked Venous Thromboembolism Academic Article
- Familial ovarian cancer. Academic Article
- Familial pericentric inversion of chromosome 19, inv(19) (p13q13) with a note on genetic counseling of pericentric inversion carriers Academic Article
- Family system characteristics and psychological adjustment to cancer susceptibility genetic testing: a prospective study Academic Article
- Five year study of prenatal testing for Huntington's disease: demand, attitudes, and psychological assessment. Academic Article
- Fryns syndrome: A rare familial cause of congenital diaphragmatic hernia Academic Article
- Gastrointestinal polyposis syndromes Academic Article
- Genetic testing for amyotrophic lateral sclerosis in Canada – an assessment of current practices Academic Article
- Genetics Consultation Rates Following a Diagnosis of High-Grade Serous Ovarian Carcinoma in the Canadian Province of Ontario Academic Article
- Genetics in obstetricians? offices: a survey study*1 Academic Article
- Hb Adana (HBA2 or HBA1: c.179G > A) and alpha thalassemia: Genotype-phenotype correlation Academic Article
- Hemoglobin H disease: not necessarily a benign disorder Academic Article
- Hemophilia in the 1990s: Principles of Management and Improved Access to Care Academic Article
- Impact of hemochromatosis gene mutations on cardiac status in doxorubicin-treated survivors of childhood high-risk leukemia Academic Article
- Information-Sharing to Promote Informed Choice in Prenatal Screening in the Spirit of the SOGC Clinical Practice Guideline: A Proposal for an Alternative Model Academic Article
- International Consensus on the Use of Genetics in the Management of Hereditary Angioedema Academic Article
- Low first-trimester pregnancy-associated plasma protein-A and Cornelia de Lange syndrome Academic Article
- Metachromatic leukodystrophy: Multiple nonfunctional and pseudodeficiency alleles in a pedigree: Problems with diagnosis and counseling Academic Article
- Midwives' views on appropriate antenatal counselling for congenital anomaly tests: do they match clients' preferences? Academic Article
- Myocardial Diseases: Current Views on Etiopathogenesis, Diagnostic Modalities, and Therapeutic Options Academic Article
- Parents’ Understanding of Genetics and Heritability Academic Article
- Periodic health examination, 1994 update: 3. Primary and secondary prevention of neural tube defects. Canadian Task Force on the Periodic Health Examination. Academic Article
- Perspectives in the Teaching of Human Genetics Academic Article
- Predictive testing for Huntington disease in Canada: Adverse effects and unexpected results in those receiving a decreased risk Academic Article
- Predictive testing for Huntington disease in Canada: The experience of those receiving an increased risk Academic Article
- Preferences of women facing a prenatal diagnostic choice: long‐term outcomes matter most Academic Article
- Prenatal Diagnosis of Hemoglobinopathies in Ontario, Canada Academic Article
- Prenatal counseling for congenital anomaly tests: parental preferences and perceptions of midwife performance Academic Article
- Prophylactic oophorectomy in Ontario. Academic Article
- Psychological consequences and predictors of adverse events in the first 5 years after predictive testing for Huntington's disease Academic Article
- Ruling in and ruling out: Implications of molecular genetic diagnoses for disease classification Academic Article
- Serum alpha - fetoprotein levels in patients with cystic fibrosis and their parents and siblings. Academic Article
- Staying informed and recontacting patients about research advances: a study of patient attitudes. Academic Article
- Stoppage rules and genetic studies of autism Academic Article
- The Duty to Recontact: Benefit and Harm Academic Article
- The Intrauterine Diagnosis of Hemoglobin Disorders Academic Article
- The Psychological Consequences of Predictive Testing for Huntington’s Disease Academic Article
- The duty to recontact: attitudes of genetics service providers. Conference Paper