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                             27 gevonden resultaten
nr titel auteur tijdschrift jaar jaarg. afl. pagina('s) type
1 Addressing uncertainty in hereditary colorectal cancer: the role of a regional expert multidisciplinary team meeting Varde, Avani

24 1 artikel
2 A family-based approach to cascade genetic testing in a pediatric cancer genetics clinic Haider, Rida

24 1 artikel
3 A novel likely pathogenic germline variant in CDKN1B in a patient with MEN4 and medullary thyroid cancer Mercè, Fernández

24 1 artikel
4 Bilateral familial retinoblastoma diagnosed via optical coherence tomography following a normal funduscopic exam Allphin, Mitchell T.

24 1 artikel
5 BRCAIndica: a resource for ACMG/AMP classified BRCA1 and BRCA2 variants Vatsyayan, Aastha

24 1 artikel
6 Cascade genetic testing in hereditary cancer: exploring the boundaries of the Italian legal framework Varesco, Liliana

24 1 artikel
7 Case review of perivascular epithelioid cell tumor occurring in patients with Li-Fraumeni syndrome Abe, Natsuno

24 1 artikel
8 CHEK2-related breast cancer: real-world challenges Weis, Luiza N.

24 1 artikel
9 Correction: Benign tumors and non-melanoma skin cancers in patients with fanconi anemia Enache, Aura

24 1 artikel
10 Correction: Outcomes of retesting in patients with previously uninformative cancer genetics evaluations Sanoba, Shenin A.

24 1 artikel
11 Germline pathogenic variants in RNF43 in patients with and without serrated polyposis syndrome Brinch, Heidi Hesselø

24 1 artikel
12 Haplotype analysis detects MLH1 founder variant in Indian Lynch syndrome patient cohort Sheth, Harsh

24 1 artikel
13 Healthcare provider-mediated cascade testing of Lynch syndrome to at-risk family members: an interview study Ong, Serene

24 1 artikel
14 Hereditary breast and ovarian cancer genetic testing in unselected patients: example of private supplementation of public healthcare service Fiorentino, Francesca

24 1 artikel
15 Identification of a germline deep intronic PTEN-deletion leading to exonization through whole genome and targeted RNA sequencing Boedec, Morgane

24 1 artikel
16 Mainstreaming cancer genetics: feasibility of an advanced nurse practitioner-led service diagnosing Lynch syndrome from colorectal cancer in Ireland Loughrey, Mechelle

24 1 artikel
17 Myelodysplastic syndrome with dual germline RUNX1 and DDX41 variants: a rare genetic predisposition case Bove, Virginia

24 1 artikel
18 New RPS20 gene variant in colorectal cancer diagnosis: insight from a large series of patients Amiot, Julie

24 1 artikel
19 Optimizing MRI sequences and apparent diffusion coefficient parameters for small pancreatic ductal adenocarcinoma detection Mori, Naoko

24 1 artikel
20 Overlap syndrome of hereditary hemorrhagic telangiectasia and juvenile polyposis syndrome: ten years follow-up-case series and review of literature Gonzalez, Maria Laura

24 1 artikel
21 Prevalence of cardiometabolic outcomes in women who underwent salpingo-oophorectomy to prevent hereditary breast and ovarian cancer: a meta-analysis Moraes, Francisco Cezar Aquino de

24 1 artikel
22 Progress report on multiple endocrine neoplasia type 1 Halperin, Reut

24 1 artikel
23 Recurrent paraneoplastic nephrotic syndrome; insights from a Lynch syndrome patient with multiple malignancies de Jong, Myrthe A.

24 1 artikel
24 Sarcomas arising in MEN1 patients: demonstrating LOH of the MEN1 locus and loss of menin expression van Leeuwaarde, Rachel S.

24 1 artikel
25 The challenge of preventing gastric cancer in patients under surveillance for familial adenomatous polyposis Bouchiba, Hicham

24 1 artikel
26 The genetic landscape of Lynch syndrome in the Israeli population Abu Shtaya, Aasem

24 1 artikel
27 Thirty-year compliance with a surveillance program for patients with familial adenomatous polyposis Cleret de Langavant, Boris

24 1 artikel
                             27 gevonden resultaten
 
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