33 results on '"Suthers, Graeme K."'
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2. Data from Lynch Syndrome–Associated Breast Cancers: Clinicopathologic Characteristics of a Case Series from the Colon Cancer Family Registry
3. Lynch syndrome-associated breast cancers do not overexpress chromosome 11-encoded mucins
4. Immunohistochemical testing of conventional adenomas for loss of expression of mismatch repair proteins in Lynch syndrome mutation carriers: a case series from the Australasian site of the colon cancer family registry
5. Rising incidence of early-onset colorectal cancer in Australia over two decades: Report and review
6. Linkage to chromosome 2q32.2-q33.3 in familial serrated neoplasia (Jass syndrome)
7. Phenotypic diversity in patients with multiple serrated polyps: a genetics clinic study
8. Analysis of families with Lynch syndrome complicated by advanced serrated neoplasia: the importance of pathology review and pedigree analysis
9. Congenital hypertrophy of the retinal pigment epithelium (CHRPE) in familial colorectal cancer
10. Erratum to: Phenotypic diversity in patients with multiple serrated polyps: a genetics clinic study
11. Letter to the editor: reply to Bousman et al.
12. Mutation detection in FGFR2 craniosynostosis syndromes
13. CANCER RISKS FOR AUSTRALIAN WOMEN WITH A BRCA1 OR A BRCA2 MUTATION
14. Frequent deletions at Xq28 indicate genetic heterogeneity in Hunter syndrome
15. Comparing the performance of gene expression assays in breast cancer
16. Deafness due to Pro250Arg mutation of FGFR3
17. Novel germ line DDX41 mutations define families with a lower age of MDS/AML onset and lymphoid malignancies
18. Diagnostic performance and costs of contingent screening models for trisomy 21 incorporating non-invasive prenatal testing
19. Recombination and the fragile X
20. Point Mutations in Exon 1B of APC Reveal Gastric Adenocarcinoma and Proximal Polyposis of the Stomach as a Familial Adenomatous Polyposis Variant
21. Rising incidence of early‐onset colorectal cancer in Australia over two decades: Report and review
22. Cancer Risks for Relatives of Patients With Serrated Polyposis
23. Heritable GATA2 mutations associated with familial myelodysplastic syndrome and acute myeloid leukemia
24. Doctors breaching patient privacy: Orwell redux
25. Alerting genetic relatives to a risk of serious inherited disease without a patient's consent
26. Linkage to chromosome 2q32.2-q33.3 in familial serrated neoplasia (Jass syndrome)
27. GATA2 is a New Predisposition Gene for Familial Myelodysplastic Syndrome (MDS) and Acute Myeloid Leukemia (AML)
28. Risk Factors for Colorectal Cancer in Patients with Multiple Serrated Polyps: A Cross-Sectional Case Series from Genetics Clinics
29. Lynch Syndrome–Associated Breast Cancers: Clinicopathologic Characteristics of a Case Series from the Colon Cancer Family Registry
30. Reply
31. Novel germ line DDX41mutations define families with a lower age of MDS/AML onset and lymphoid malignancies
32. GATA2is a New Predisposition Gene for Familial Myelodysplastic Syndrome (MDS) and Acute Myeloid Leukemia (AML)
33. Rising incidence of early-onset colorectal cancer in Australia over two decades: report and review
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