Hereditary gastric cancer: what’s new? Update 2013–2018
来源期刊:Familial CancerDOI:10.1007/s10689-019-00127-7
Moving into the mainstream: healthcare professionals’ views of implementing treatment focussed genetic testing in breast cancer care
来源期刊:Familial CancerDOI:10.1007/s10689-019-00122-y
Inequities in multi-gene hereditary cancer testing: lower diagnostic yield and higher VUS rate in individuals who identify as Hispanic, African or Asian and Pacific Islander as compared to European
来源期刊:Familial CancerDOI:10.1007/s10689-019-00144-6
Implication of DNA repair genes in Lynch-like syndrome
来源期刊:Familial CancerDOI:10.1007/s10689-019-00128-6
Novel candidates in early-onset familial colorectal cancer
来源期刊:Familial CancerDOI:10.1007/s10689-019-00145-5
Hereditary diffuse gastric cancer: cancer risk and the personal cost of preventive surgery
来源期刊:Familial CancerDOI:10.1007/s10689-019-00133-9
Ability of known susceptibility SNPs to predict colorectal cancer risk for persons with and without a family history
来源期刊:Familial CancerDOI:10.1007/s10689-019-00136-6
Long-term positive psychological outcomes in an Australian pancreatic cancer screening program
来源期刊:Familial CancerDOI:10.1007/s10689-019-00147-3
Should unaffected female BRCA2 pathogenic variant carriers be told there is little or no advantage from risk reducing mastectomy?
来源期刊:Familial CancerDOI:10.1007/s10689-019-00142-8
Renal cell carcinoma in young FH mutation carriers: case series and review of the literature
来源期刊:Familial CancerDOI:10.1007/s10689-019-00155-3
‘We don’t know for sure’: discussion of uncertainty concerning multigene panel testing during initial cancer genetic consultations
来源期刊:Familial CancerDOI:10.1007/s10689-019-00154-4
Genetic counseling referral for ovarian cancer patients: a call to action
来源期刊:Familial CancerDOI:10.1007/s10689-019-00129-5
Pediatric craniopharyngioma in association with familial adenomatous polyposis
来源期刊:Familial CancerDOI:10.1007/s10689-019-00126-8
The incidence of consecutive manifestations in Von Hippel-Lindau disease
来源期刊:Familial CancerDOI:10.1007/s10689-019-00131-x
Radiotherapy-induced malignancies in breast cancer patients with TP53 pathogenic germline variants (Li–Fraumeni syndrome)
来源期刊:Familial CancerDOI:10.1007/s10689-019-00153-5
TP53 variants of uncertain significance: increasing challenges in variant interpretation and genetic counseling
来源期刊:Familial CancerDOI:10.1007/s10689-019-00140-w
Health behaviours and beliefs in individuals with familial pancreatic cancer
来源期刊:Familial CancerDOI:10.1007/s10689-019-00143-7
Mutated SON putatively causes a cancer syndrome comprising high-risk medulloblastoma combined with café-au-lait spots
来源期刊:Familial CancerDOI:10.1007/s10689-019-00121-z
Phenotypic confirmation of oligodontia, colorectal polyposis and cancer in a family carrying an exon 7 nonsense variant in the AXIN2 gene
来源期刊:Familial CancerDOI:10.1007/s10689-019-00120-0
Implementation of a Systematic Tumor Screening Program for Lynch Syndrome in an Integrated Health Care Setting
来源期刊:Familial CancerDOI:10.1007/s10689-019-00123-x
Progress report: familial pancreatic cancer
来源期刊:Familial CancerDOI:10.1007/s10689-019-00125-9
Exploring the preferences of involved health professionals regarding the implementation of an online decision aid to support couples during reproductive decision-making in hereditary cancer: a mixed methods approach
来源期刊:Familial CancerDOI:10.1007/s10689-019-00119-7
Multiple primary malignancies associated with a germline SMARCB1 pathogenic variant
来源期刊:Familial CancerDOI:10.1007/s10689-019-00138-4
Energy balance related lifestyle factors and risk of endometrial and colorectal cancer among individuals with lynch syndrome: a systematic review
来源期刊:Familial CancerDOI:10.1007/s10689-019-00135-7
MLH1 promoter hypermethylation: are you absolutely sure about the absence of MLH1 germline mutation? About a new case
来源期刊:Familial CancerDOI:10.1007/s10689-019-00151-7
The (ir)relevance of the abandoned criterion II for the diagnosis of serrated polyposis syndrome: a retrospective cohort study
来源期刊:Familial CancerDOI:10.1007/s10689-019-00156-2
Population frequencies of pathogenic alleles of BRCA1 and BRCA2: analysis of 173 Danish breast cancer pedigrees using the BOADICEA model
来源期刊:Familial CancerDOI:10.1007/s10689-019-00141-9
Lynch syndrome with exclusive skin involvement: time to consider a molecular definition?
来源期刊:Familial CancerDOI:10.1007/s10689-019-00139-3
Targeted next generation sequencing screening of Lynch syndrome in Tunisian population
来源期刊:Familial CancerDOI:10.1007/s10689-019-00130-y
A unique case of two somatic APC mutations in an early onset cribriform-morular variant of papillary thyroid carcinoma and overview of the literature
来源期刊:Familial CancerDOI:10.1007/s10689-019-00146-4
International society for gastrointestinal hereditary tumours—InSiGHT
来源期刊:Familial CancerDOI:10.1007/s10689-019-00124-w
Assessing a single SNP located at TERT/CLPTM1L multi-cancer risk region as a genetic modifier for risk of pancreatic cancer and melanoma in Dutch CDKN2A mutation carriers
来源期刊:Familial CancerDOI:10.1007/s10689-019-00137-5
De novo pathogenic germline variant in PALB2 in a patient with pancreatic cancer
来源期刊:Familial CancerDOI:10.1007/s10689-019-00157-1
Clear cell chondrosarcoma in Von Hippel-Lindau disease
来源期刊:Familial CancerDOI:10.1007/s10689-019-00149-1
Endoscopic full thickness resection for early colon cancer in Lynch syndrome
来源期刊:Familial CancerDOI:10.1007/s10689-019-00132-w