subject area of
- A Practical Guide to the Management of the Fetus and Newborn With Hemophilia Journal Articles
- A qualitative study of women and partners from Lebanon and Quebec regarding an expanded scope of noninvasive prenatal testing Journal Articles
- A rare subtelomeric deletion syndrome: Wolf Hirschhorn syndrome. Journal Articles
- A unique BRCA1 mutation identified in Mongolia Journal Articles
- Age at clinical onset and at ultrasonographic detection of adult polycystic kidney disease: Data for genetic counselling Journal Articles
- Alpha-thalassaemia and population health in Southeast Asia Journal Articles
- Breast and ovarian cancer risk perception after prophylactic salpingo‐oophorectomy due to an inherited mutation in the BRCA1 or BRCA2 gene Journal Articles
- Cancer prevention and screening in a BRCA2-positive male to female transgender patient Journal Articles
- Clinical genetics provider real-time workflow study Journal Articles
- Coinheritance of α-thalassemia-1 and hemoglobin E/β0-thalassemia: Practical implications for neonatal screening and genetic counseling Journal Articles
- Cross-cultural perspectives on decision making regarding noninvasive prenatal testing: A comparative study of Lebanon and Quebec Journal Articles
- Data sharing as a national quality improvement program: reporting on BRCA1 and BRCA2 variant-interpretation comparisons through the Canadian Open Genetics Repository (COGR) Journal Articles
- Decision Analysis of Prenatal Testing for Chromosomal Disorders: What Do the Preferences of Pregnant Women Tell Us? Journal Articles
- Delivery of molecular genetic services within a health care system: time analysis of the clinical workload. The Molecular Genetic Study Group. Journal Articles
- Development and Pilot Evaluation of Novel Genetic Educational Materials Designed for an Underserved Patient Population Journal Articles
- Double heterozygosity for germline mutations in BRCA1 and p53 in a woman with early onset breast cancer Journal Articles
- Evaluation of a decision aid for incidental genomic results, the Genomics ADvISER: protocol for a mixed methods randomised controlled trial Journal Articles
- Evolution of genetic assessment for BRCA-associated gynaecologic malignancies: a Canadian multisociety roadmap Journal Articles
- Factors That Predict Risk of Thrombosis in Relatives of Patients With Unprovoked Venous Thromboembolism Journal Articles
- Familial ovarian cancer. Journal Articles
- Family system characteristics and psychological adjustment to cancer susceptibility genetic testing: a prospective study Journal Articles
- Gastrointestinal polyposis syndromes Journal Articles
- Genetic testing for amyotrophic lateral sclerosis in Canada – an assessment of current practices Journal Articles
- Genetics Adviser: a protocol for a mixed-methods randomised controlled trial evaluating a digital platform for genetics service delivery Journal Articles
- Genetics Consultation Rates Following a Diagnosis of High-Grade Serous Ovarian Carcinoma in the Canadian Province of Ontario Journal Articles
- Genetics in obstetricians? offices: a survey study*1 Journal Articles
- Genomic testing in cancer: Patient knowledge, attitudes, and expectations Journal Articles
- Hb Adana (HBA2 or HBA1: c.179G > A) and alpha thalassemia: Genotype–phenotype correlation Journal Articles
- Hemoglobin H disease: not necessarily a benign disorder Journal Articles
- Hemophilia in the 1990s: Principles of Management and Improved Access to Care Journal Articles
- Impact of hemochromatosis gene mutations on cardiac status in doxorubicin‐treated survivors of childhood high‐risk leukemia Journal Articles
- Information-Sharing to Promote Informed Choice in Prenatal Screening in the Spirit of the SOGC Clinical Practice Guideline: A Proposal for an Alternative Model Journal Articles
- International Consensus on the Use of Genetics in the Management of Hereditary Angioedema Journal Articles
- Low first‐trimester pregnancy‐associated plasma protein‐A and Cornelia de Lange syndrome Journal Articles
- Metachromatic leukodystrophy: Multiple nonfunctional and pseudodeficiency alleles in a pedigree: Problems with diagnosis and counseling Journal Articles
- Midwives' views on appropriate antenatal counselling for congenital anomaly tests: Do they match clients' preferences? Journal Articles
- Midwives' views on appropriate antenatal counselling for congenital anomaly tests: do they match clients' preferences? Journal Articles
- Myocardial Diseases: Current Views on Etiopathogenesis, Diagnostic Modalities, and Therapeutic Options Journal Articles
- Parents’ Understanding of Genetics and Heritability Journal Articles
- Periodic health examination, 1994 update: 3. Primary and secondary prevention of neural tube defects. Canadian Task Force on the Periodic Health Examination. Journal Articles
- Perspectives in the Teaching of Human Genetics Journal Articles
- Preferences of women facing a prenatal diagnostic choice: long‐term outcomes matter most Journal Articles
- Prenatal Diagnosis of Hemoglobinopathies in Ontario, Canada Journal Articles
- Prenatal counseling for congenital anomaly tests: parental preferences and perceptions of midwife performance Journal Articles
- Prophylactic oophorectomy in Ontario. Journal Articles
- RETIRED: Fetal and Perinatal Autopsy in Prenatally Diagnosed Fetal Abnormalities With Normal Karyotype Journal Articles
- Rates of genetic consultation in high-grade serous ovarian cancer patients in the era of PARP inhibitor therapy: A population-based study. Journal Articles
- Ruling in and ruling out: Implications of molecular genetic diagnoses for disease classification Journal Articles
- Serum alpha - fetoprotein levels in patients with cystic fibrosis and their parents and siblings. Journal Articles
- Stoppage rules and genetic studies of autism Journal Articles
- The Intrauterine Diagnosis of Hemoglobin Disorders Journal Articles