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Nature genetics, ISSN 1061-4036, 05/2009, Volume 41, Issue 5, pp. 585 - 590
Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | Fundamental and applied biological sciences. Psychology | Classical genetics, quantitative genetics, hybrids | Gynecology. Andrology. Obstetrics | Mammary gland diseases | Biological and medical sciences | Genetics of eukaryotes. Biological and molecular evolution | Medical sciences | Methods, theories and miscellaneous | Tumors | Genetic Predisposition to Disease - genetics | Breast Neoplasms - genetics | Breast Neoplasms - pathology | Humans | Disease Susceptibility - metabolism | Female | Genotype | Chromosome Mapping | Genome, Human | Chromosomes, Human, Pair 17 - genetics | Chromosomes, Human, Pair 3 - genetics | Breast cancer | Genetic aspects | Disease susceptibility | Research | Single nucleotide polymorphisms | Risk factors | Medical research | Genetic markers | Gene loci | Hospitals | Regression analysis | chromosome 3 | Index Medicus | Medicin och hälsovetenskap
Journal Article
Nature genetics, ISSN 1061-4036, 03/2016, Volume 48, Issue 4, pp. 374 - 386
Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | Gene Expression | Genetic Predisposition to Disease | Genetic Association Studies | Humans | Risk Factors | Cell Cycle Proteins - metabolism | Gene Expression Regulation, Neoplastic | Chromosomes, Human, Pair 6 - genetics | Breast Neoplasms - metabolism | Carrier Proteins - genetics | Phenotype | Breast Neoplasms - genetics | Carrier Proteins - metabolism | Estrogen Receptor alpha - genetics | Base Sequence | Cell Cycle Proteins - genetics | Protein Binding | Estrogen Receptor alpha - metabolism | Female | Polymorphism, Single Nucleotide | Genetic variation | Breast cancer | Genetic aspects | Gene expression | Properties | Health aspects | Identification and classification | Risk factors | Index Medicus | Clinical Medicine | Medical and Health Sciences | Klinisk medicin | Cancer and Oncology | Medicin och hälsovetenskap | Cancer och onkologi
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Full Text
Irbesartan in Marfan syndrome (AIMS): a double-blind, placebo-controlled randomised trial
The Lancet (British edition), ISSN 0140-6736, 12/2019, Volume 394, Issue 10216, pp. 2263 - 2270
Medicine, General & Internal | Life Sciences & Biomedicine | General & Internal Medicine | Science & Technology | Echocardiography | Aorta - diagnostic imaging | Double-Blind Method | Drug Administration Schedule | Aorta - drug effects | Humans | Male | Treatment Outcome | United Kingdom | Angiotensin II Type 1 Receptor Blockers - pharmacology | Young Adult | Marfan Syndrome - drug therapy | Adolescent | Adult | Female | Marfan Syndrome - diagnostic imaging | Irbesartan - administration & dosage | Child | Angiotensin II Type 1 Receptor Blockers - administration & dosage | Irbesartan - pharmacology | Irbesartan | Clinical trials | Marfan syndrome | Marfan's syndrome | Young adults | Sensitivity analysis | Laboratories | Complications | Research | Diameters | Randomization | Consent | Angiotensin | Aorta | Blood pressure | Adults | Mutation | Children | Mercury | Stretching | Index Medicus | Abridged Index Medicus
Journal Article
Scientific reports, ISSN 2045-2322, 12/2018, Volume 8, Issue 1, pp. 285 - 285
Science & Technology - Other Topics | Multidisciplinary Sciences | Science & Technology | Forests | Phenotype | Quantitative Trait, Heritable | Tropical Climate | Plant Leaves | Biological Variation, Population | Plants | Biodiversity | Costa Rica | Economics | Leaves | Succession | Drought resistance | Ordination | Environmental changes | Ontogeny | Leaf area | Variation | Species | Index Medicus
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5.
Dracula
2017, East Central and Eastern Europe in the Middle Ages, 450-1450, ISBN 9004347259, Volume 46, xxxiii, 457 pages
Book
The Lancet (British edition), ISSN 0140-6736, 02/2019, Volume 393, Issue 10173, pp. 747 - 757
Medicine, General & Internal | Life Sciences & Biomedicine | General & Internal Medicine | Science & Technology | Fetus - abnormalities | Congenital Abnormalities - epidemiology | Fetus - diagnostic imaging | Prospective Studies | Humans | Parents | Perinatal Death - etiology | Male | DNA Copy Number Variations - genetics | Whole Exome Sequencing - methods | Abnormal Karyotype - embryology | Congenital Abnormalities - diagnosis | Pregnancy | Abortion, Spontaneous - epidemiology | Congenital Abnormalities - genetics | Nuchal Translucency Measurement | Stillbirth - epidemiology | Abnormal Karyotype - statistics & numerical data | Female | Live Birth - epidemiology | Fetal Development - genetics | Abortion, Eugenic - statistics & numerical data | Infant, Newborn | Whole Exome Sequencing - statistics & numerical data | Ultrasound imaging | Pregnant women | Heart | Intellectual disabilities | Copy number | Genes | Disorders | Prenatal development | Aneuploidy | Genomes | Gestation | Microcephaly | Genetic screening | Gene sequencing | Disability | Proteins | Parents & parenting | Ultrasonic imaging | Next-generation sequencing | Scoliosis | Heart diseases | Ultrasound | Deoxyribonucleic acid--DNA | Phenotypes | Congenital diseases | Research & development--R&D | Fetuses | Abnormalities | Birth defects | Heredity | Hearing impairment | Coronary artery disease | Genetic variance | DNA microarrays | Gene frequency | Diagnostic systems | Cardiovascular diseases | Anomalies | Index Medicus | Abridged Index Medicus
Journal Article
Nature genetics, ISSN 1061-4036, 06/2010, Volume 42, Issue 6, pp. 504 - 507
Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | Fundamental and applied biological sciences. Psychology | Gynecology. Andrology. Obstetrics | Mammary gland diseases | Biological and medical sciences | Genetics of eukaryotes. Biological and molecular evolution | Medical sciences | Tumors | Genetic Predisposition to Disease | Genome-Wide Association Study | Breast Neoplasms - genetics | Humans | Female | Genotype | Chromosomes, Human, Pair 11 | Chromosomes, Human, Pair 8 | Polymorphism, Single Nucleotide | Chromosomes, Human, Pair 9 | Chromosomes, Human, Pair 6 | Chromosomes, Human, Pair 10 | Gene mutations | Breast cancer | Genetic aspects | Disease susceptibility | Diagnosis | Research | Single nucleotide polymorphisms | Health aspects | Risk factors | Studies | Medical research | Genetics | Family medical history | Index Medicus
Journal Article