| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Absence of the RET+3:T allele in the MTC patients
|
Borun, Pawel
|
|
2012
|
10 |
1 |
|
artikel
|
| 2 |
A Pilot study of the Sharing Risk Information Tool (ShaRIT) for Families with Hereditary Breast and Ovarian Cancer Syndrome
|
Kardashian, Ani
|
|
2012
|
10 |
1 |
|
artikel
|
| 3 |
Birt-Hogg-Dube syndrome presenting as multiple oncocytic parotid tumors
|
Lindor, Noralane M
|
|
2012
|
10 |
1 |
|
artikel
|
| 4 |
BRAF mutations in thyroid tumors from an ethnically diverse group
|
Schulten, Hans-Juergen
|
|
2012
|
10 |
1 |
|
artikel
|
| 5 |
Challenges in the management of a patient with Cowden syndrome: case report and literature review
|
Melbārde-Gorkuša, Inga
|
|
2012
|
10 |
1 |
|
artikel
|
| 6 |
Chemokine Ligand 5 (CCL5) and chemokine receptor (CCR5) genetic variants and prostate cancer risk among men of African Descent: a case-control study
|
Kidd, LaCreis R
|
|
2012
|
10 |
1 |
|
artikel
|
| 7 |
Close ties: an exploratory Colored Eco-Genetic Relationship Map (CEGRM) study of social connections of men in Familial Testicular Cancer (FTC) families
|
Peters, June A
|
|
2012
|
10 |
1 |
|
artikel
|
| 8 |
Determining the functional significance of mismatch repair gene missense variants using biochemical and cellular assays
|
Heinen, Christopher D
|
|
2012
|
10 |
1 |
|
artikel
|
| 9 |
Diagnostic and pathogenetic role of café-au-lait macules in nevoid basal cell carcinoma syndrome
|
Ponti, Giovanni
|
|
2012
|
10 |
1 |
|
artikel
|
| 10 |
DNA and RNA analyses in detection of genetic predisposition to cancer
|
Kurzawski, Grzegorz
|
|
2012
|
10 |
1 |
|
artikel
|
| 11 |
Factors influencing receptivity to future screening options for pancreatic cancer in those with and without pancreatic cancer family history
|
Breitkopf, Carmen Radecki
|
|
2012
|
10 |
1 |
|
artikel
|
| 12 |
Familial gastric cancer: detection of a hereditary cause helps to understand its etiology
|
Vogelaar, Ingrid P
|
|
2012
|
10 |
1 |
|
artikel
|
| 13 |
Family perspectives in lynch syndrome becoming a family at risk, patterns of communication and influence on relations
|
Bartuma, Katarina
|
|
2012
|
10 |
1 |
|
artikel
|
| 14 |
Novel germline CDK4 mutations in patients with head and neck cancer
|
Sabir, Maimoona
|
|
2012
|
10 |
1 |
|
artikel
|
| 15 |
Novel germline MSH2 mutation in lynch syndrome patient surviving multiple cancers
|
Janavicius, Ramunas
|
|
2012
|
10 |
1 |
|
artikel
|
| 16 |
Prevalance of BRCA1 and BRCA2 mutations in familial breast cancer patients in Lebanon
|
Jalkh, Nadine
|
|
2012
|
10 |
1 |
|
artikel
|
| 17 |
Rare vertebral metastasis in a case of Hereditary Paraganglioma
|
da Silva, Manuel Eduardo Ribeiro
|
|
2012
|
10 |
1 |
|
artikel
|
| 18 |
The R337H mutation in TP53 and breast cancer in Brazil
|
Gomes, Magda CB
|
|
2012
|
10 |
1 |
|
artikel
|
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