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You searched for: Author/Creator Verhoef, Senno

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1. An unbalanced submicroscopic translocation t(8;16)(q24.3;p13.3)pat associated with tuberous sclerosis complex, adult polycystic kidney disease, and hypomelanosis of Ito. Issue 4 (1st April 2000)

2. Breast and ovarian cancer risks in a large series of clinically ascertained families with a high proportion of BRCA1 and BRCA2 Dutch founder mutations. Issue 2 (27th November 2013)

3. Comprehensive Mutation Analysis of PMS2 in a Large Cohort of Probands Suspected of Lynch Syndrome or Constitutional Mismatch Repair Deficiency Syndrome. Issue 11 (21st August 2016)

4. Do BRCA1/2 mutation carriers have an earlier onset of natural menopause?. Issue 8 (August 2016)

5. Do BRCA1/2 mutation carriers have an earlier onset of natural menopause?. Issue 8 (August 2016)

6. Functional analysis of MSH2 unclassified variants found in suspected Lynch syndrome patients reveals pathogenicity due to attenuated mismatch repair. Issue 4 (5th February 2014)

7. Identification of independent association signals and putative functional variants for breast cancer risk through fine-scale mapping of the 12p11 locus. Issue 1 (December 2016)

8. Mutational spectrum of the TSC1 gene in a cohort of 225 tuberous sclerosis complex patients: no evidence for genotype-phenotype correlation. Issue 4 (1st April 1999)

9. No evidence that protein truncating variants in BRIP1 are associated with breast cancer risk: implications for gene panel testing. Issue 5 (26th February 2016)

10. PALB2, CHEK2 and ATM rare variants and cancer risk: data from COGS. Issue 12 (5th September 2016)