Found: 20
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RSK2 mutation co-segregates with X-linked intellectual disability and attenuated Coffin-Lowry phenotype in a three-generation family.
- Published in:
- Clinical Genetics, 2014, v. 85, n. 1, p. 96, doi. 10.1111/cge.12122
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- Article
Geographical distribution of Slovenian BRCA1/2 families according to family origin: implications for genetic screening.
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- Clinical Genetics, 2014, v. 85, n. 1, p. 59, doi. 10.1111/cge.12119
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- Article
High prevalence of BRCA1 founder mutations in Greek breast/ovarian families.
- Published in:
- Clinical Genetics, 2014, v. 85, n. 1, p. 36, doi. 10.1111/cge.12274
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- Article
Genomic signatures of BRCA1 but not BRCA2 associated high-grade serous carcinoma resemble basal-like breast cancer.
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- Clinical Genetics, 2014, v. 85, n. 1, p. 16, doi. 10.1111/cge.12302
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- Article
Delineating the effects BRCA1 and BRCA2 loss of heterozygosity in pancreatic cancer progression.
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- Clinical Genetics, 2014, v. 85, n. 1, p. 18, doi. 10.1111/cge.12306
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- Article
The uptake and outcome of prenatal and pre-implantation genetic diagnosis for Huntington's disease in the Netherlands (1998-2008).
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- Clinical Genetics, 2014, v. 85, n. 1, p. 87, doi. 10.1111/cge.12089
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- Article
Breast cancer genetics: 20 years later.
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- Clinical Genetics, 2014, v. 85, n. 1, p. 5, doi. 10.1111/cge.12293
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- Article
The psychological impact of breast and ovarian cancer preventive options in BRCA1 and BRCA2 mutation carriers.
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- Clinical Genetics, 2014, v. 85, n. 1, p. 7, doi. 10.1111/cge.12298
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- Article
The spectrum of BRCA1 and BRCA2 mutations in breast cancer patients in the Bahamas.
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- Clinical Genetics, 2014, v. 85, n. 1, p. 64, doi. 10.1111/cge.12132
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- Article
Risk of having BRCA1 mutation in high-risk women with triple-negative breast cancer: a meta-analysis.
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- Clinical Genetics, 2014, v. 85, n. 1, p. 43, doi. 10.1111/cge.12270
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- Article
Prenatal testing for Huntington's disease in the Netherlands from 1998 to 2008.
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- Clinical Genetics, 2014, v. 85, n. 1, p. 78, doi. 10.1111/cge.12090
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- Article
Clinical implications of genetic testing for BRCA1 and BRCA2 mutations in Austria.
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- Clinical Genetics, 2014, v. 85, n. 1, p. 72, doi. 10.1111/cge.12216
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- Article
Linking distant relatives with BRCA gene mutations: potential for cost savings.
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- Clinical Genetics, 2014, v. 85, n. 1, p. 54, doi. 10.1111/cge.12211
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- Publication type:
- Article
BRCA1/2 negative status predicts no extended risk of invasive ovarian cancer.
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- Clinical Genetics, 2014, v. 85, n. 1, p. 17, doi. 10.1111/cge.12303
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- Article
Health care provider recommendations for reducing cancer risks among women with a BRCA1 or BRCA2 mutation.
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- Clinical Genetics, 2014, v. 85, n. 1, p. 21, doi. 10.1111/cge.12233
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- Article
BRCA1 and BRCA2 - update and implications on the genetics of breast cancer: a clinical perspective.
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- Clinical Genetics, 2014, v. 85, n. 1, p. 1, doi. 10.1111/cge.12291
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- Article
Rates of risk-reducing surgery in Israeli BRCA1 and BRCA2 mutation carriers.
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- Clinical Genetics, 2014, v. 85, n. 1, p. 68, doi. 10.1111/cge.12149
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- Article
Modes of delivery of genetic testing services and the uptake of cancer risk management strategies in BRCA1 and BRCA2 carriers.
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- Clinical Genetics, 2014, v. 85, n. 1, p. 49, doi. 10.1111/cge.12130
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- Article
Screening for BRCA1 and BRCA2 mutations among French-Canadian breast cancer cases attending an outpatient clinic in Montreal.
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- Clinical Genetics, 2014, v. 85, n. 1, p. 31, doi. 10.1111/cge.12174
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- Article
Huntington disease in 2013 - genetic choices across the life cycle.
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- Clinical Genetics, 2014, v. 85, n. 1, p. 76, doi. 10.1111/cge.12093
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- Article