10 results on '"Bakry, Doua"'
Search Results
2. TP53 Germline Mutations: Genetics of Li–Fraumeni Syndrome
3. Gastrointestinal Findings in the Largest Series of Patients With Hereditary Biallelic Mismatch Repair Deficiency Syndrome: Report from the International Consortium
4. Phenotypic and genotypic characterisation of biallelic mismatch repair deficiency (BMMR-D) syndrome
5. 548 Gastrointestinal (GI) Findings in Patients With Biallelic Mismatch Repair (BMMRD) Gene Deficiency Syndrome: Report From the International Consortium
6. BRAF Mutation and CDKN2A Deletion Define a Clinically Distinct Subgroup of Childhood Secondary High-Grade Glioma
7. Abstract 35: Novel genetic and clinical determinants of Constitutional Mismatch Repair Deficiency syndrome: Report from the CMMRD consortium
8. Genetic and clinical determinants of constitutional mismatch repair deficiency syndrome: Report from the constitutional mismatch repair deficiency consortium
9. Abstract 1435: Phenotype:Genotype correlations of p53 mutation carriers: The 20-year Toronto experience
10. Permanent Neonatal Diabetes Caused by Glucokinase Deficiency
Catalog
Books, media, physical & digital resources
Discovery Service for Jio Institute Digital Library
For full access to our library's resources, please sign in.