35 results on '"El-Haffaf, Zaki"'
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2. A functionally impaired missense variant identified in French Canadian families implicates FANCI as a candidate ovarian cancer-predisposing gene
3. Current gene panels account for nearly all homologous recombination repair-associated multiple-case breast cancer families
4. Whether, when, how, and how much? General public’s and cancer patients’ views about the disclosure of genomic secondary findings
5. OR08-05 Case Series Of French Canadian Patients With Paragangliomas Carrying The c.397C>T SDHC Mutation: Insights On SDHC Phenotype And Outcomes
6. FRI157 Systematic Germline Genetic Analysis In A Cohort Of Adults With Primary Aldosteronism And Hypertension Onset ≤35 yo : Low Yield Of Genetic Pathogenic Variants
7. Langerhans cell histiocytosis presenting as Crohn’s disease: a case report
8. Clinical follow-up and breast and ovarian cancer screening of true BRCA1/2 noncarriers: a qualitative investigation
9. A comparative analysis of RAS variants in patients with disorders of somatic mosaicism
10. Molecular Genetic Characteristics of FANCI, a Proposed New Ovarian Cancer Predisposing Gene
11. Atypical ADPKD Due to a DNAJB11 Pathogenic Variant: An Educational Case Report
12. Supplemental Materials: Genetic Dissection of Primary Aldosteronism in a Patient With MEN1 and Ipsilateral Adrenocortical Carcinoma and Adenoma
13. Amyloid Deposits in a Functionally Unicuspid Stenotic Aortic Valve
14. QOL-25. IMPACTS OF IMPLEMENTING A PROSPECTIVE TREATMENT AND SURVEILLANCE PROTOCOL FOR THE MANAGEMENT OF NF2-ASSOCIATED VESTIBULAR SCHWANNOMAS ON TUMOR GROWTH, HEARING OUTCOMES, AND QUALITY OF LIFE
15. Genetic Dissection of Primary Aldosteronism in a Patient With MEN1 and Ipsilateral Adrenocortical Carcinoma and Adenoma
16. The Genetic and Molecular Analyses of RAD51C and RAD51D Identifies Rare Variants Implicated in Hereditary Ovarian Cancer from a Genetically Unique Population
17. Case Review: Whole-Exome Sequencing Analyses Identify Carriers of a Known Likely Pathogenic Intronic BRCA1 Variant in Ovarian Cancer Cases Clinically Negative for Pathogenic BRCA1 and BRCA2 Variants
18. eP362: Mosaic RAS family in-frame insertion variants in patients with hemangiomas and vascular malformations
19. Genetic analyses of DNA repair pathway associated genes implicate new candidate cancer predisposing genes in ancestrally defined ovarian cancer cases.
20. Genetic Dissection of Primary Aldosteronism in a Patient With MEN1 and Ipsilateral Adrenocortical Carcinoma and Adenoma.
21. A decade of RAD51C and RAD51D germline variants in cancer
22. Additional file 3 of A functionally impaired missense variant identified in French Canadian families implicates FANCI as a candidate ovarian cancer-predisposing gene
23. Additional file 1 of Whether, when, how, and how much? General public’s and cancer patients’ views about the disclosure of genomic secondary findings
24. Additional file 2 of Whether, when, how, and how much? General public’s and cancer patients’ views about the disclosure of genomic secondary findings
25. Additional file 2 of A functionally impaired missense variant identified in French Canadian families implicates FANCI as a candidate ovarian cancer-predisposing gene
26. Additional file 4 of A functionally impaired missense variant identified in French Canadian families implicates FANCI as a candidate ovarian cancer-predisposing gene
27. The genetic analysis of a founder Northern American population of European descent identifiesFANCIas a candidate familial ovarian cancer risk gene
28. Cancer Risks Associated With Germline PALB2 Pathogenic Variants: An International Study of 524 Families
29. A decade of RAD51C and RAD51D germline variants in cancer.
30. Cancer Risks Associated With Germline PALB2 Pathogenic Variants: An International Study of 524 Families
31. SUN-373 Small Adrenal Incidentaloma Stable in Size Becoming a Stage IV Adrenocortical Carcinoma 10 Years Later in a Young Patient Carrying a Germline APC Variant of Uncertain Significance (VUS)
32. Clinical follow-up and breast and ovarian cancer screening of true BRCA1/2noncarriers: a qualitative investigation
33. A comparative analysis of RASvariants in patients with disorders of somatic mosaicism
34. eP362: Mosaic RASfamily in-frame insertion variants in patients with hemangiomas and vascular malformations
35. A functionally impaired missense variant identified in French Canadian families implicates FANCI as a candidate ovarian cancer-predisposing gene
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