المؤلفون: Jamie M Ellingford, Ryan George, John H McDermott, Shazaad Ahmad, Jonathan J Edgerley, David Gokhale, William G Newman, Stephen Ball, Nicholas Machin, Graeme CM Black

المصدر: eLife, Vol 10 (2021)

مصطلحات موضوعية: SARS-CoV-2, genome, sequencing, healthcare worker, healthcare-associated, nosocomial, Medicine, Science, Biology (General), QH301-705.5

وصف الملف: electronic resource

العلاقة: https://elifesciences.org/articles/65453Test; https://doaj.org/toc/2050-084XTest

الوصول الحر: https://doaj.org/article/ccd0a2e9674f422e9315dcf5926a5603Test

المؤلفون: David Gokhale, Diane Cairns, Victoria McKay, Lynn Greenhalgh, Roger Mountford

المصدر: Familial Cancer. 15:57-61

مصطلحات موضوعية: Male, 0301 basic medicine, congenital, hereditary, and neonatal diseases and abnormalities, Cancer Research, Nonsense mutation, Peutz-Jeghers Syndrome, STK11, Peutz–Jeghers syndrome, Protein Serine-Threonine Kinases, 030105 genetics & heredity, Biology, medicine.disease_cause, Frameshift mutation, 03 medical and health sciences, Exon, 0302 clinical medicine, AMP-Activated Protein Kinase Kinases, Genetics, medicine, Humans, Multiplex ligation-dependent probe amplification, skin and connective tissue diseases, Genetics (clinical), Mutation, Mosaicism, medicine.disease, Human genetics, Oncology, 030220 oncology & carcinogenesis, Cancer research, Female, Multiplex Polymerase Chain Reaction

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7450cec6224b42d7351b95e25d804b1bTest
https://doi.org/10.1007/s10689-015-9839-3Test

المؤلفون: Maria Panayi, Rob Elles, Sahar Mansour, David Gokhale

المصدر: Prenatal Diagnosis. 25:930-933

مصطلحات موضوعية: Pathology, medicine.medical_specialty, L1, Gestational Age, Neural Cell Adhesion Molecule L1, Prenatal diagnosis, Polymerase Chain Reaction, Central nervous system disease, Pregnancy, Prenatal Diagnosis, medicine, Humans, Point Mutation, Missense mutation, Agenesis of the corpus callosum, Genetics (clinical), X chromosome, business.industry, Point mutation, Obstetrics and Gynecology, Genetic Diseases, X-Linked, DNA, Syndrome, medicine.disease, Pedigree, nervous system diseases, Hydrocephalus, Chorionic Villi Sampling, Mutation, Female, business, Gene Deletion

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::aa268df39a19209edf34d37c529d0415Test
https://doi.org/10.1002/pd.1228Test

المؤلفون: Edited Sian Ellard, Ruth Charlton, Michael Yau, David Gokhale, Graham R Taylor, Simon C Ramsden, Ratified Cmgs, Executive Committee August

المساهمون: The Pennsylvania State University CiteSeerX Archives

المصدر: http://www.cmgs.org/BPGs/pdfsTest current bpgs/Sequencingv2.pdf.

وصف الملف: application/pdf

العلاقة: http://citeseerx.ist.psu.edu/viewdoc/summary?doi=10.1.1.486.4607Test; http://www.cmgs.org/BPGs/pdfsTest current bpgs/Sequencingv2.pdf

الإتاحة: http://www.cmgs.org/BPGs/pdfsTest current bpgs/Sequencingv2.pdf

المؤلفون: Malcolm Taylor, David Gokhale, William Fergusson, Colin W. Summers

المصدر: The Lancet. 339:621

مصطلحات موضوعية: Genetics, Polymorphism, Genetic, Histocompatibility Testing, Single-strand conformation polymorphism, DNA, General Medicine, Biology, law.invention, HLA-DR locus, medicine.anatomical_structure, Investigation methods, HLA Antigens, law, HLA-DQ locus, Nucleic acid, medicine, Humans, Nucleic Acid Conformation, Bone marrow, Polymerase chain reaction, Bone Marrow Transplantation, Single-Strand Conformation Polymorphism Analysis

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6e2b6302fd1e6d591b534c316e869d6eTest
https://doi.org/10.1016/0140-6736Test(92)90911-l