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在“
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”中,
命中:
6,510
条,耗时:小于0.01 秒
在所有数据库中总计命中:
16,161
条
1.
Hereditary
cancer syndromes in Latino populations: genetic characterization and surveillance guidelines
作者:
Marcia Cruz-Correa
;
Julyann Pérez-Mayoral…
关键词:
Genetic testing
;
Genetic counseling
;
Germline mutations
;
Hereditary
cancer
;
Hispanics
刊名:
Hereditary
Cancer in Clinical Practice
出版年:2017
2.
Anxiety and depression symptoms among women attending group-based patient education courses for
hereditary
breast and ovarian cancer
作者:
Wenche Listøl
;
Hildegunn Høberg-Vetti…
关键词:
Group
;
based patient education course
;
Genetic counseling
;
Hereditary
cancer
;
Anxiety symptoms
;
Depression symptoms
刊名:
Hereditary
Cancer in Clinical Practice
出版年:2017
3.
DNA copy number profiling in microsatellite-stable and microsatellite-unstable
hereditary
non-polyposis colorectal cancers by targeted CNV array
作者:
Weixiang Chen
;
Jun Ding
;
Long Jiang
;
Zebing Liu…
关键词:
Colorectal cancer
;
Hereditary
non
;
polyposis colorectal cancer
;
Microsatellite stable
;
Copy number
;
Loss of heterozygosity
刊名:Functional & Integrative Genomics
出版年:2017
4.
The impact of
hereditary
multiple exostoses on quality of life, satisfaction, global health status, and pain
作者:
Riccardo D’Ambrosi
;
Vincenza Ragone…
关键词:
Hereditary
multiple exostoses
;
Quality of life
;
Global health status
;
Rare disease
;
Pain
;
Satisfaction
;
Surgical procedure
刊名:Archives of Orthopaedic and Trauma Surgery
出版年:2017
5.
Hereditary
breast and ovarian cancer: successful systematic implementation of a group approach to genetic counselling
作者:
Patrick R. Benusiglio
;
Marina Di Maria
;
Leila Dorling
;
Anne Jouinot…
关键词:
Genetic counselling
;
Delivery of health care
;
Patient education
;
BRCA1
;
BRCA2
;
Hereditary
breast and ovarian cancer syndrome
刊名:Familial Cancer
出版年:2017
6.
ALS and MMN mimics in patients with
BSCL2
mutations: the expanding clinical spectrum of SPG17
hereditary
spastic paraplegia
作者:
Thomas Musacchio
;
Ann-Kathrin Zaum
;
Nurcan Üçeyler
;
Claudia Sommer…
关键词:
Hereditary
spastic paraplegia
;
SPG17
;
BSCL2
刊名:Journal of Neurology
出版年:2017
7.
Frequency of pathogenic germline mutation in
CHEK2, PALB2, MRE11
, and
RAD50
in patients at high risk for
hereditary
breast cancer
作者:
Haeyoung Kim
;
Dae-Yeon Cho
;
Doo Ho Choi
;
Mijin Oh…
关键词:
CHEK2
;
PARB2
;
MRE11
;
RAD50
;
Hereditary
breast and ovarian cancer syndrome
刊名:Breast Cancer Research and Treatment
出版年:2017
8.
Georgia Primary Care Providers’ Knowledge of
Hereditary
Breast and Ovarian Cancer Syndrome
作者:
Navya Nair
;
Cecelia Bellcross
;
Lisa Haddad
;
Monique Martin…
关键词:
Hereditary
;
BRCA
;
Breast cancer
;
Ovarian cancer
刊名:Journal of Cancer Education
出版年:2017
9.
Hereditary
hemorrhagic telangiectasia, liver disease and elevated serum testosterone (Osler–Weber–Rendu syndrome): a case report
作者:
R. Dissanayake
;
K. P. K. Y. M. D. S. Wickramarathne…
关键词:
Hereditary
hemorrhagic telangiectasia
;
Arterio venous malformation
;
Liver nodules
;
Elevated serum testosterone
刊名:BMC Research Notes
出版年:2017
10.
Quality of life in patients with
hereditary
haemorrhagic telangiectasia (HHT)
作者:
Roberto Zarrabeitia
;
Concepción Fariñas-Álvarez…
关键词:
HHT
;
Hereditary
hemorrhagic telangiectasia
;
Rendu Osler
;
Euroqol
;
Qol
刊名:Health and Quality of Life Outcomes
出版年:2017
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作者(19)
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