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The New England journal of medicine, ISSN 1533-4406, 2007, Volume 356, Issue 3, pp. 237 - 247
Journal Article
Hereditary cancer in clinical practice, ISSN 1897-4287, 2019, Volume 17, Issue 1, pp. 14 - 8
Background: Pathogenic variants in BRCA1 and BRCA2 cause hereditary breast and ovarian cancer. Screening of these genes has become easily accessible in... 
BREAST-CANCER | Splicing | ONCOLOGY | RT-PCR | POLYPYRIMIDINE TRACT | Variant classification | mRNA | BRCA1 | OVARIAN-CANCER | BRCA2 | Variant of unknown significance | Messenger RNA | Analysis | Genetic research | Genetic aspects | Genetic transcription | Research | Diagnosis | Ovarian cancer | Cancer | Consortia | BRCA2 protein | BRCA1 protein | Laboratories | Copy number | Genes | Classification | Reverse transcription | Breast cancer | Mutation
Journal Article
Hereditary cancer in clinical practice, ISSN 1897-4287, 2018, Volume 16, Issue 1, pp. 3 - 15
...Author(s): Cecilie Heramb[sup.1,2,3], Teresia Wangensteen[sup.1], Eli Marie Grindedal[sup.1], Sarah Louise Ariansen[sup.1], Sheba Lothe[sup.4], Ketil... 
Founder mutations | BRCA1 | Genetic testing | BRCA2 | POPULATION | RISKS | BRCA2 MUTATIONS | SEQUENCE VARIANTS | OVARIAN-CANCER | FAMILY-HISTORY | CARRIERS | BREAST | ONCOLOGY | EPIDEMIOLOGY | Prevention | Gene mutations | Medical care | Genetic aspects | Genetic screening | Cancer | Quality management | Usage | Research | BRCA mutations
Journal Article
Molecular genetics & genomic medicine, ISSN 2324-9269, 2019, Volume 7, Issue 9, pp. e889 - n/a
Journal Article
Familial cancer, ISSN 1573-7292, 2020, Volume 19, Issue 2, pp. 133 - 142
... Schlichting5,6 · Tone Vamre1 · Teresia Wangensteen1 · Cecilie Heramb1 · Lovise Mæhle1 Published online: 30 January 2020 © The Author(s) 2020 Abstract Studies have shown... 
POLY(ADP-RIBOSE) POLYMERASE | RISKS | MUTATION CARRIERS | GUIDELINES | Breast cancer | Mainstreaming cancer genetics | BRCA1 | FAMILY-HISTORY | BRCA | WOMEN | ONCOLOGY | GENETICS & HEREDITY | OVARIAN | Genetic testing | Genetic counseling | Hospitals | Patients | Genetic screening | Original
Journal Article
ISSN 2324-9269, 2019
Background Genetic risk variants in the hemizygous allele may influence neuropsychiatric manifestations and clinical course in 3q29 deletion carriers. Methods... 
Journal Article
Tidsskrift for den Norske Laegeforening, ISSN 0029-2001, 11/2005, Volume 125, Issue 22, pp. 3090 - 3093
Journal Article
Tidsskrift for den Norske Laegeforening, ISSN 0029-2001, 12/2003, Volume 123, Issue 24, pp. 3549 - 3552
Journal Article
Tidsskrift for den Norske Lægeforening, 11/2005, Volume 125, Issue 22, p. 3090
Overweight and obesity represent an increasing health problem. Both genetic and environmental factors contribute to the development of obesity. This article... 
Receptors, Leptin | Appetite - genetics | Genetic Predisposition to Disease | Humans | Risk Factors | Overweight - genetics | Receptor, Melanocortin, Type 4 - genetics | Obesity - genetics | Syndrome | Obesity, Morbid - genetics | Adult | Obesity - etiology | Child | Receptors, Cell Surface - genetics
Journal Article
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