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Nature genetics, ISSN 1061-4036, 02/2019, Volume 51, Issue 2, pp. 230 - 236
Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | Genetic Predisposition to Disease - genetics | Humans | Middle Aged | Male | United Kingdom | Case-Control Studies | Osteoarthritis, Hip - genetics | Biological Specimen Banks | Polymorphism, Single Nucleotide - genetics | Adult | Female | Aged | Genome-Wide Association Study - methods | Quantitative Trait Loci - genetics | Knee | Fibroblast growth factor | Target recognition | Disease | Genes | Interleukin | Clinical trials | Animal diseases | Mapping | Genomes | Arthritis | Joint replacement surgery | Body mass index | Pain | Animal tissues | Interleukin 1 | Extracellular matrix | Biocompatibility | Fibroblast growth factor 18 | Bioinformatics | Growth factors | Medical research | Phenotypes | Cathepsin K | Transforming growth factor-b1 | Therapeutic applications | Interleukin 11 | Gene expression | Loci | Hip | Quantitative trait loci | Studies | Collagen | Gene mapping | Osteoarthritis | Index Medicus
Journal Article
The Yorkshire post (Leeds, England : 1959), 11/2019
Newspaper Article
European journal of human genetics : EJHG, ISSN 1018-4813, 01/2013, Volume 21, Issue 1, pp. 82 - 88
speech delay | array CGH | ELKS/ERC1 gene | 12p13.33 | childhood apraxia of speech (CAS) | inherited deletion | Biochemistry & Molecular Biology | Genetics & Heredity | Life Sciences & Biomedicine | Science & Technology | Chromosome Deletion | Genetic Predisposition to Disease | Language Development Disorders - genetics | Humans | Child, Preschool | In Situ Hybridization, Fluorescence | Male | Apraxias - etiology | Nerve Tissue Proteins - genetics | Pregnancy | Apraxias - genetics | Adaptor Proteins, Signal Transducing - genetics | Family | Female | Speech | Chromosomes, Human, Pair 12 | France | Child | Phenotypes | Language disorders | Genes | Cognitive ability | Heredity | Genomes | Sound | Patients | Autism | Hypotheses | Databases | DVD | Clonal deletion | Collaboration | Genetics | Chromosome 12 | Children | Mutation | Speech disorders | Index Medicus | Telomeres | speech | Gene deletion | ERC1 gene | ELKS
Journal Article
European journal of human genetics : EJHG, ISSN 1018-4813, 10/2010, Volume 18, Issue 10, pp. 1095 - 1099
abnormal hand movement | array CGH | monoamine oxidase | X chromosome | MAOA and MAOB | Biochemistry & Molecular Biology | Genetics & Heredity | Life Sciences & Biomedicine | Science & Technology | Fundamental and applied biological sciences. Psychology | General aspects. Genetic counseling | Medical genetics | Biological and medical sciences | Molecular and cellular biology | Genetics of eukaryotes. Biological and molecular evolution | Medical sciences | Chromosomes, Human, X - genetics | Muscle Hypotonia - genetics | Chromosomes, Human, X - ultrastructure | Humans | Male | Developmental Disabilities - genetics | Monoamine Oxidase - genetics | Intellectual Disability - genetics | Monoamine Oxidase - deficiency | Gene Deletion | Stereotyped Behavior | Polymerase Chain Reaction | Epilepsy - genetics | Dyskinesias - genetics | Index Medicus
Journal Article
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Constitutional and somatic rearrangement of chromosome 21 in acute lymphoblastic leukaemia
Nature (London), ISSN 0028-0836, 2014, Volume 508, Issue 1, pp. 98 - 102
Science & Technology - Other Topics | Multidisciplinary Sciences | Science & Technology | Precursor Cell Lymphoblastic Leukemia-Lymphoma - genetics | Chromatids - genetics | Humans | Chromosome Aberrations | Recombination, Genetic - genetics | DNA Copy Number Variations - genetics | Chromosomes, Human, Pair 15 - genetics | Chromosomes, Human, Pair 21 - genetics | Chromosome Breakage | Translocation, Genetic - genetics | Hypotheses | Hematology | Leukemia | Cytogenetics | Gene expression | Chromosomes | Cancer | Index Medicus
Journal Article
The New England journal of medicine, ISSN 0028-4793, 10/2008, Volume 359, Issue 16, pp. 1685 - 1699
Journal Article
International journal of cancer, ISSN 0020-7136, 09/2019, Volume 145, Issue 6, pp. 1493 - 1498
chromosome aberrations | epidemiology | cohort studies | mortality | breast cancer | cytogenetics | neoplasms | Life Sciences & Biomedicine | Oncology | Science & Technology | Translocation, Genetic | Genetic Predisposition to Disease | Prospective Studies | Humans | Middle Aged | Child, Preschool | Neoplasms - mortality | Infant | Male | Incidence | Young Adult | Neoplasms - genetics | Adolescent | Aged, 80 and over | Adult | Heterozygote | Aged | Chromosomes, Human, Pair 11 | Chromosomes, Human, Pair 22 | Child | United Kingdom - epidemiology | Infant, Newborn | Neoplasms - epidemiology | Oncology, Experimental | Mortality | Cytogenetics | Research | Health aspects | Epidemiology | Cancer | Translocation | Robertsonian translocation | Invasiveness | Health risks | Aneuploidy | Breast cancer | Carriers | Offspring | Infertility | Health risk assessment | Index Medicus | Cancer Epidemiology
Journal Article
Developmental medicine and child neurology, ISSN 0012-1622, 10/2009, Volume 51, Issue 10, pp. 833 - 837
Pediatrics | Clinical Neurology | Neurosciences & Neurology | Life Sciences & Biomedicine | Science & Technology | Chromosome Deletion | Pain Insensitivity, Congenital - genetics | Humans | Child, Preschool | Female | Nerve Growth Factor - genetics | Chromosomes, Human, Pair 1 - genetics | Index Medicus
Journal Article
American journal of epidemiology, ISSN 0002-9262, 03/2019, Volume 188, Issue 3, pp. 500 - 508
Life Sciences & Biomedicine | Public, Environmental & Occupational Health | Science & Technology | Protein Translocation Systems - analysis | Humans | Middle Aged | Risk Factors | Neoplasms - mortality | Male | Lymphoma, Non-Hodgkin - genetics | Incidence | Young Adult | Neoplasms - genetics | Adolescent | Aged, 80 and over | Adult | Female | Heterozygote | Aged | Lymphoma, Non-Hodgkin - mortality | Child | United Kingdom - epidemiology | Leukemia - genetics | Cohort Studies | Leukemia - mortality | Translocation | Robertsonian translocation | Leukemia | Mortality | Health risks | Risk | Breast cancer | Lymphoma | Carriers | Confidence intervals | Chromosome translocations | Offspring | Risk assessment | Infertility | Cytogenetics | Children | Health risk assessment | Chromosomes | Age | Hodgkin's disease | Index Medicus | hematological malignancies | chromosome disorders | epidemiology | genetics | Original Contributions | cohort studies | mortality | cytogenetics | neoplasms
Journal Article
Nature genetics, ISSN 1061-4036, 11/2018
Journal Article
Nature genetics, ISSN 1061-4036, 2018, Volume 50, pp. 1752 - 1755
Journal Article
Nature genetics, ISSN 1061-4036, 11/2016, Volume 48, Issue 11, pp. 1303 - 1312
Journal Article
American journal of human genetics, ISSN 0002-9297, 11/2016
Journal Article