subject area of
- A DNA marker closely linked to the factor IX (haemophilia B) gene Journal Articles
- A Multicenter Trial of the Effectiveness of ζ-Globin Enzyme-Linked Immunosorbent Assay and Hemoglobin H Inclusion Body Screening for the Detection of α0-Thalassemia Trait Journal Articles
- A novel monoclonal antibody based diagnostic test for alpha-thalassemia- 1 carriers due to the (-SEA/) deletion Journal Articles
- A single strand conformation polymorphism study of CD40 ligand. Efficient mutation analysis and carrier detection for X-linked hyper IgM syndrome. Journal Articles
- An assessment of the use of flanking DNA markers for fra(X) syndrome carrier detection and prenatal diagnosis Journal Articles
- Carrier detection and prenatal diagnosis of hemoglobinopathies in Ontario. Journal Articles
- Carrier detection in the hemophilias Journal Articles
- Carrier detection of haemophilia A using DNA markers in families with an isolated affected male Journal Articles
- Carrier detection strategy in haemophilia A: the benefits of combined DNA marker analysis and coagulation testing in sporadic haemophilic families Journal Articles
- Cholesterol Metabolism and Suicidality in Smith-Lemli-Opitz Syndrome Carriers Journal Articles
- Clonal origin of human basophil/mast cells from circulating multipotent hemopoietic progenitors. Journal Articles
- Compound Heterozygosity For Triplicated α‐Globin Gene and (– –SEA) α‐Globin Gene Deletion: Implication For Thalassaemia Screening Journal Articles
- DHCR7 and Smith-Lemli-Opitz syndrome. Journal Articles
- Distribution of CFTR mutations in Saguenay– Lac-Saint-Jean: proposal of a panel of mutations for population screening Journal Articles
- Fixed-bin analysis for statistical evaluation of continuous distributions of allelic data from VNTR loci, for use in forensic comparisons. Journal Articles
- Frequency and ethnic distribution of the commonDHCR7 mutation in Smith-Lemli-Opitz syndrome Journal Articles
- Genetic mapping of X-linked albinism-deafness syndrome (ADFN) to Xq26.3-q27.I. Journal Articles
- Hemophilia B (Christmas disease) variants and carrier detection analyzed by DNA probes. Journal Articles
- Hemophilia in the 1990s: Principles of Management and Improved Access to Care Journal Articles
- High functioning autism and Childhood Disintegrative Disorder in half brothers. Journal Articles
- Human embryonic zeta-globin chain expression in deletional alpha- thalassemias Journal Articles
- Identification of a novel β0 ‐ thalassaemia mutation in a greek family and subsequent prenatal diagnosis Journal Articles
- Immunocytological test to detect adult carriers of (--SEA/) deletional α-thalassaemia Journal Articles
- Individual and family characteristics associated with protein truncating BRCA1 and BRCA2 mutations in an Ontario population based series from the Cooperative Family Registry for Breast Cancer Studies Journal Articles
- Mutation Analysis in F9 Gene of 17 Families with Haemophilia B from Iran Conferences
- Potential Application of a New Screening Test for α-Thalassemia-1 Carriers Journal Articles
- Prenatal Diagnosis of Hemoglobinopathies in Ontario, Canada Journal Articles
- Protein C deficiency and thromboembolism: recurrent mutation at Arg 306 in the protein C gene Journal Articles
- Reduced Excitatory Neurotransmission and Mild Autism-Relevant Phenotypes in AdolescentShank3Null Mutant Mice Journal Articles
- Routine Screening of (--<sup>SEA</sup>) α-Thalassemia Deletion by an Enzyme-Linked Immunosorbent Assay for Embryonic ζ-Globin Chains Journal Articles
- Smith-Lemli-Opitz syndrome: carrier frequency and spectrum of DHCR7 mutations in Canada Journal Articles
- Spontaneous and therapeutic abortions and the risk of breast cancer among BRCAmutation carriers Journal Articles
- The Genetic Distance between the Coagulation Factor IX Gene and the Locus for the Fragile X Syndrome: Clinical Implications Journal Articles
- Treatment of Two Infants with Cooley's Anemia with Sodium Phenylbutyrate Journal Articles
- Variability of clinical manifestation of factor VII-deficiency in homozygous and heterozygous subjects of the European F7 gene mutation A294V Journal Articles
- β‐thalassemia in association with a new δ‐chain hemoglobin variant [δ116(g18)Arg→Leu]: Implications for carrier screening and prenatal diagnosis Journal Articles