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2011, ISBN 0691123179, 368
.... The Enculturated Gene traces how this genetic discourse has blotted from view the roles that Senegalese patients and doctors have played in making sickle cell "mild" in a social setting where public... 
Social aspects | Senegal | Sickle cell anemia | Services for | Genetic disorders | Sociology | Kinship | Anthropology | Genetic aspects | History | Patients | Health aspects | SOCIAL SCIENCE | Disease & Health Issues | Cultural
eBook
American journal of obstetrics and gynecology, ISSN 0002-9378, 2017, Volume 217, Issue 5, pp. 512 - 521
... for the majority of mutations encountered by gynecologists, newly identified deleterious genetic mutations continue... 
Obstetrics and Gynecology | BRCA | risk reduction | screening | ovarian cancer | high risk | endometrial cancer | hereditary cancer | cervical cancer | Lynch syndrome | Life Sciences & Biomedicine | Obstetrics & Gynecology | Science & Technology | Genetic Testing | DNA Polymerase III - genetics | Hereditary Breast and Ovarian Cancer Syndrome - diagnosis | Humans | Li-Fraumeni Syndrome - diagnosis | DNA Mismatch Repair - genetics | Tumor Suppressor Protein p53 - genetics | Genital Neoplasms, Female - diagnosis | Li-Fraumeni Syndrome - genetics | Epithelial Cell Adhesion Molecule - genetics | Genes, BRCA2 | Female | RNA Helicases - genetics | Lynch Syndrome II - genetics | Neoplastic Syndromes, Hereditary - genetics | Genes, BRCA1 | Genital Neoplasms, Female - genetics | Hereditary Breast and Ovarian Cancer Syndrome - genetics | PTEN Phosphohydrolase - genetics | Genetic Predisposition to Disease | Hamartoma Syndrome, Multiple - genetics | Fanconi Anemia Complementation Group Proteins - genetics | Protein-Serine-Threonine Kinases - genetics | Neoplastic Syndromes, Hereditary - diagnosis | MutS Homolog 2 Protein - genetics | DNA-Binding Proteins - genetics | Peutz-Jeghers Syndrome - genetics | Hamartoma Syndrome, Multiple - diagnosis | MutL Protein Homolog 1 - genetics | Peutz-Jeghers Syndrome - diagnosis | Lynch Syndrome II - diagnosis | Mismatch Repair Endonuclease PMS2 - genetics | Gene mutations | Endometrial cancer | Diagnosis | Cervical cancer | Genetic screening | Cancer | Ovarian cancer | Index Medicus | Abridged Index Medicus
Journal Article
Journal of clinical oncology, ISSN 1527-7755, 04/2017, Volume 35, Issue 10, pp. 1086 - 1095
Journal Article
Cancer, ISSN 0008-543X, 05/2017, Volume 123, Issue 10, pp. 1721 - 1730
Journal Article
Cancer, ISSN 0008-543X, 10/2017, Volume 123, Issue 20, pp. 3925 - 3932
BACKGROUND Prostate cancer has a significant heritable component, and rare deleterious germline variants in certain genes can increase the risk of the disease.... 
prostate cancer | germline variants | multiple primary malignant neoplasms | genetic testing | gene panel | Life Sciences & Biomedicine | Oncology | Science & Technology | Humans | Middle Aged | Male | Mutation, Missense | Checkpoint Kinase 2 - genetics | Prostatic Neoplasms - genetics | DNA Mutational Analysis | Tumor Suppressor Proteins - genetics | Aged, 80 and over | Germ-Line Mutation | Adult | RNA Helicases - genetics | Neoplastic Syndromes, Hereditary - genetics | Neoplasms, Second Primary - genetics | Nuclear Proteins - genetics | Fanconi Anemia Complementation Group N Protein | Receptor, Fibroblast Growth Factor, Type 3 - genetics | Genetic Predisposition to Disease | Neoplastic Syndromes, Hereditary - diagnosis | DNA-Binding Proteins - genetics | Fanconi Anemia Complementation Group Proteins | Sequence Analysis, DNA | Homeodomain Proteins - genetics | MutL Protein Homolog 1 - genetics | Age of Onset | Aged | Ataxia Telangiectasia Mutated Proteins - genetics | BRCA2 Protein - genetics | Care and treatment | Genetic aspects | Research | Gene mutations | Genetic variation | Prostate cancer | Fibroblast growth factor | Genes | DNA damage | Homology | Malignancy | Criteria | DNA repair | Genetic screening | Homeobox | DNA helicase | Proteins | Ataxia | Genetics | Deoxyribonucleic acid--DNA | Fibroblast growth factor receptor 3 | BRCA2 protein | CHK2 protein | Nucleotide sequence | BRCA1 protein | MLH1 protein | Health risks | Protein C | Breast cancer | Medical screening | Patients | Medical prognosis | Men | Ataxia telangiectasia mutated protein | Mutation | Prostate | Cancer | Fibroblast growth factor receptors | Index Medicus | Abridged Index Medicus
Journal Article
Molecular cell, ISSN 1097-2765, 07/2018, Volume 71, Issue 1, pp. 25 - 41.e6
Journal Article
PLoS genetics, ISSN 1553-7404, 03/2011, Volume 7, Issue 3, pp. e1001357 - e1001357
Journal Article
PloS one, ISSN 1932-6203, 03/2014, Volume 9, Issue 3, pp. e92506 - e92506
Background: Genetic variation at loci influencing adult levels of HbF have been shown to modify the clinical course of sickle cell disease (SCD... 
Science & Technology - Other Topics | Multidisciplinary Sciences | Science & Technology | Prognosis | Follow-Up Studies | Humans | Middle Aged | Child, Preschool | Hospitalization - statistics & numerical data | Proto-Oncogene Proteins c-myb - genetics | Male | Erythrocytes, Abnormal - metabolism | GTP-Binding Proteins - genetics | Young Adult | Haplotypes - genetics | Anemia, Sickle Cell - epidemiology | Polymerase Chain Reaction | Adult | Female | Nuclear Proteins - genetics | Child | Peptide Elongation Factors - genetics | Fetal Hemoglobin - metabolism | African Americans - genetics | HSP70 Heat-Shock Proteins - genetics | Carrier Proteins - genetics | Erythrocytes, Abnormal - pathology | Phenotype | Cameroon - epidemiology | Polymorphism, Restriction Fragment Length | Anemia, Sickle Cell - metabolism | Adolescent | Polymorphism, Single Nucleotide - genetics | Anemia, Sickle Cell - genetics | Medical research | Sickle cell anemia | African Americans | Medicine, Experimental | Medical records | Hemoglobin | Hydroxyurea | Research | Comparative analysis | Blood transfusion | Haplotypes | Health sciences | Transfusion | Single-nucleotide polymorphism | Blood | Gene sequencing | Ethics | Demographics | Genetic analysis | Chromosome 11 | Genetics | Electrophoresis | Population | Mathematical models | Sickle cell disease | Chromosomes | Public health | Parasitology | Statistical analysis | Hematology | Capillary electrophoresis | Fetuses | Genetic diversity | Minority & ethnic groups | Patients | Loci | HBB gene | Homozygotes | Medicine | Statistical models | Infectious diseases | Genotyping | Gene frequency | Influence | Mutation | Index Medicus
Journal Article