"Familial risk" trang 1 - tải miễn phí từ tailieuXANH
Cancer risks in Lynch syndrome, Lynch-like syndrome, and familial colorectal cancer type X: A prospective cohort study

Cancer risks in Lynch syndrome, Lynch-like syndrome, and familial colorectal cancer type X: A prospective cohort study
11    69    0
Family-specific, novel, deleterious germline variants provide a rich resource to identify genetic predispositions for BRCAx familial breast cancer

Family-specific, novel, deleterious germline variants provide a rich resource to identify genetic predispositions for BRCAx familial breast cancer
11    64    0
Familial risk and protective factors in alcohol intoxicated adolescents: Psychometric evaluation of the family domain of the Communities That Care Youth Survey (CTC) and a new short version of the Childhood Trauma Questionnaire (CTQ)

Familial risk and protective factors in alcohol intoxicated adolescents: Psychometric evaluation of the family domain of the Communities That Care Youth Survey (CTC) and a new short version of the Childhood Trauma Questionnaire (CTQ)
14    41    0
The contribution of the rs55705857 G allele to familial cancer risk as estimated in the Utah population database

The contribution of the rs55705857 G allele to familial cancer risk as estimated in the Utah population database
6    59    0
Familial breast cancer - The classification and care of women at risk of familial breast cancer in primary, secondary and tertiary care

Familial breast cancer - The classification and care of women at risk of familial breast cancer in primary, secondary and tertiary care

50    39    0
Broadening risk profile in familial colorectal cancer type X; increased risk for five cancer types in the national Danish cohort

Broadening risk profile in familial colorectal cancer type X; increased risk for five cancer types in the national Danish cohort
10    99    0
Stellate cells and mesenchymal stem cells in benign mammary stroma are associated with risk factors for breast cancer – an observational study

Stellate cells and mesenchymal stem cells in benign mammary stroma are associated with risk factors for breast cancer – an observational study
13    78    0
Using a state cancer registry to recruit young breast cancer survivors and high-risk relatives: Protocol of a randomized trial testing the efficacy of a targeted versus a tailored intervention to increase breast cancer screening

Using a state cancer registry to recruit young breast cancer survivors and high-risk relatives: Protocol of a randomized trial testing the efficacy of a targeted versus a tailored intervention to increase breast cancer screening
9    210    0
Breast ductal lavage for biomarker assessment in high risk women: Rationale, design and methodology of a randomized phase II clinical trial with nimesulide, simvastatin and placebo

Breast ductal lavage for biomarker assessment in high risk women: Rationale, design and methodology of a randomized phase II clinical trial with nimesulide, simvastatin and placebo
10    59    0
Báo cáo y học:

Báo cáo y học: "Improving calculation, interpretation and communication of familial colorectal cancer risk: Protocol for a randomized controlled trial"
7    32    0
báo cáo khoa học:

báo cáo khoa học: " Improving calculation, interpretation and communication of familial colorectal cancer risk: Protocol for a randomized controlled trial"
7    35    0
Predictors of mammographic density among women with a strong family history of breast cancer

Predictors of mammographic density among women with a strong family history of breast cancer
12    81    0
CATCHing putative causative variants in consanguineous families

CATCHing putative causative variants in consanguineous families
5    62    0
A burden of rare variants in BMPR2 and KCNK3 contributes to a risk of familial pulmonary arterial hypertension

A burden of rare variants in BMPR2 and KCNK3 contributes to a risk of familial pulmonary arterial hypertension
8    41    1
A novel mutation of KCNQ2 gene in a patient with self-limited non-familial neonatal epilepsy: A case report

A novel mutation of KCNQ2 gene in a patient with self-limited non-familial neonatal epilepsy: A case report
8    42    1
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