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1دورية أكاديمية
المؤلفون: D. Hettiarachchi, S. M. V. Subasinghe, G. G. Anandagoda, Hetalkumar Panchal, P. S. Lai, V. H. W. Dissanayake
المصدر: BMC Medical Genomics, Vol 15, Iss 1, Pp 1-8 (2022)
مصطلحات موضوعية: Internal medicine, RC31-1245, Genetics, QH426-470
وصف الملف: electronic resource
Relation: https://doaj.org/toc/1755-8794
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2دورية أكاديمية
المؤلفون: D. Hettiarachchi, Hetalkumar Panchal, P. S. Lai, V. H. W. Dissanayake
المصدر: BMC Medical Genetics, Vol 21, Iss 1, Pp 1-7 (2020)
مصطلحات موضوعية: CHILD syndrome, X-linked dominant, NSDHL gene, Novel variant, Syndactyly, Internal medicine, RC31-1245, Genetics, QH426-470
وصف الملف: electronic resource
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3دورية أكاديمية
المصدر: Journal of Pure and Applied Microbiology, Vol 14, Iss suppl 1, Pp 849-860 (2020)
مصطلحات موضوعية: covid-19, sars-cov-2, sars-cov, mers-cov, pandemic, who, Microbiology, QR1-502
وصف الملف: electronic resource
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4دورية أكاديمية
المؤلفون: D. Hettiarachchi, Hetalkumar Panchal, B. A. P. S. Pathirana, P. D. Rathnayaka, A. Padeniya, P. S. Lai, V. H. W. Dissanayake
المصدر: Case Reports in Genetics, Vol 2020 (2020)
وصف الملف: electronic resource
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5دورية أكاديمية
المصدر: Genomics Data, Vol 8, Iss C, Pp 52-60 (2016)
مصطلحات موضوعية: PCOS, Phylogenetic analysis, MeV, String, Modeller, RaptorX, Microarray, Genetics, QH426-470
وصف الملف: electronic resource
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6دورية أكاديمية
المصدر: Genomics Data, Vol 7, Iss , Pp 189-194 (2016)
وصف الملف: electronic resource
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7
المؤلفون: A. Padeniya, P D Rathnayaka, Hetalkumar Panchal, D. Hettiarachchi, B. A. P. S. Pathirana, P. S. Lai, Vajira H. W. Dissanayake
المصدر: Case Reports in Genetics, Vol 2020 (2020)
Case Reports in Geneticsمصطلحات موضوعية: Genetics, Sanger sequencing, congenital, hereditary, and neonatal diseases and abnormalities, Chromosome, Chorea, General Medicine, QH426-470, Biology, medicine.disease, Compound heterozygosity, symbols.namesake, Exon, Ataxia-telangiectasia, medicine, symbols, Case Series, medicine.symptom, Gene, Myoclonus
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::47e40efd10b4c37b5f5466b0accec5ee
https://doi.org/10.1155/2020/6630300 -
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المؤلفون: P. S. Lai, Hetalkumar Panchal, D. Hettiarachchi, V. H. W. Dissanayake
المصدر: BMC Medical Genetics
BMC Medical Genetics, Vol 21, Iss 1, Pp 1-7 (2020)مصطلحات موضوعية: 0301 basic medicine, Proband, lcsh:Internal medicine, medicine.medical_specialty, 3-Hydroxysteroid Dehydrogenases, lcsh:QH426-470, Limb Deformities, Congenital, Mutation, Missense, Erythroderma, Case Report, 030105 genetics & heredity, Protein Structure, Secondary, 03 medical and health sciences, Protein Domains, Catalytic Domain, Internal medicine, Genetics, medicine, Animals, Humans, Missense mutation, Abnormalities, Multiple, Genetic Predisposition to Disease, Syndactyly, lcsh:RC31-1245, Conserved Sequence, Genetic Association Studies, Genetics (clinical), Exome sequencing, X-linked dominant, business.industry, CHILD syndrome, Genodermatosis, Infant, Genetic Diseases, X-Linked, Ichthyosiform Erythroderma, Congenital, medicine.disease, Novel variant, Hypoplasia, lcsh:Genetics, 030104 developmental biology, Endocrinology, Mutation, Female, NSDHL gene, business
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المؤلفون: Gauravi Trivedi, Janhavi T. Karlekar, Hetalkumar Panchal
المصدر: SSRN Electronic Journal.
مصطلحات موضوعية: Drug, G protein, Mechanism (biology), Cell growth, Apoptosis, Chemistry, In silico, media_common.quotation_subject, Target protein, Computational biology, Ligand (biochemistry), media_common
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::edbb2689559d799c5827e9eeed7d17ed
https://doi.org/10.2139/ssrn.3570339 -
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