المؤلفون: Viorica Radoi, Andrei Kozma, Vasilica Toma, Horia Lăzărescu, Radu Ursu, Agnes Katherine Lackner, Laurențiu Camil Bohîlțea, Norina Forna

المصدر: Romanian Journal of Oral Rehabilitation, Vol 11, Iss 2, Pp 90-95 (2019)

مصطلحات موضوعية: oro-dental anomalies, genetic testing, Kallman syndrome, Noonan syndrome, Dentistry, RK1-715

وصف الملف: electronic resource

العلاقة: http://www.rjor.ro/differential-diagnosis-and-genetic-testing-for-determining-the-molecular-causes-underlying-oro-dental-anomalies-in-a-series-of-patientsTest/; https://doaj.org/toc/2066-7000Test; https://doaj.org/toc/2601-4661Test

الوصول الحر: https://doaj.org/article/a105987f9bd84a04a46f9d6944db98ecTest

المؤلفون: Andrei Kozma, Doriana Agop Forna, Viorica Radoi, Radu Ursu, Agnes Katalin Lackner, Laurentiu Camil Bohiltea, Horia Lazarescu

المصدر: Romanian Journal of Stomatology, Vol 65, Iss 2, Pp 97-100 (2019)

مصطلحات موضوعية: enamel, genetics, amelogenesis imperfecta, Medicine, Dentistry, RK1-715

وصف الملف: electronic resource

العلاقة: https://rjs.com.ro/articles/2019.2/RJS_2019_2_Art-01.pdfTest; https://doaj.org/toc/1843-0805Test; https://doaj.org/toc/2069-6078Test

الوصول الحر: https://doaj.org/article/27904ada8362456e92183ec672e5b106Test

المؤلفون: Andrei Kozma, Doriana Agop Forna, Viorica Rădoi, Radu Ursu, Laurențiu Camil Bohâlțea

المصدر: Romanian Journal of Medical and Dental Education, Vol 8, Iss 1, Pp 15-19 (2019)

مصطلحات موضوعية: Genetics, cleft lip, palate, genome-wide association studies (GWAS), Dentistry, RK1-715

وصف الملف: electronic resource

العلاقة: http://journal.adre.ro/genetic-factors-involved-in-the-development-of-cleft-lip-and-or-palateTest/; https://doaj.org/toc/2393-1108Test; https://doaj.org/toc/2393-1531Test

الوصول الحر: https://doaj.org/article/b507b6a810bb4cccbe330b97bc6a45c2Test

المؤلفون: Andrei Kozma, Doriana Agop Forna, Viorica Radoi, Ana Maria Alexandra Stanescu, Radu Ursu, Laurentiu Camil Bohaltea

المصدر: Romanian Medical Journal, Vol 65, Iss 4, Pp 258-260 (2018)

مصطلحات موضوعية: dentinogenesis, osteogenesis, gene panel, Medicine (General), R5-920, Surgery, RD1-811

وصف الملف: electronic resource

العلاقة: https://revistemedicale.amaltea.ro/Romanian_MEDICAL_Journal/Revista_MEDICALA_ROMANA-2018-Nr.4/RMJ_2018_4_Art-03.pdfTest; https://doaj.org/toc/1220-5478Test; https://doaj.org/toc/2069-606XTest

الوصول الحر: https://doaj.org/article/fba0f8e2083f4878a2565c746d2abe48Test

المؤلفون: Viorica Radoi, Delia Ileana Sabau, Radu Ursu, Laurentiu Bohiltea, Oana Toader, Lucian Pop

مصطلحات موضوعية: Bilateral anophthalmia, Clitoris agenesis, Labia minora agenesis, SOX2, Syndromic

العلاقة: https://zenodo.org/record/4625105Test; https://doi.org/10.5281/zenodo.4625105Test; oai:zenodo.org:4625105

الإتاحة: https://doi.org/10.5281/zenodo.4625105Test
https://doi.org/10.5281/zenodo.4625104Test
https://zenodo.org/record/4625105Test

المؤلفون: Viorica Radoi, Florentina Gherghiceanu, Dragos Cretoiu, Irina Balescu, Radu Ursu, Nicolae Bacalbasa, Daniela Oana Toader, Florentina Furtunescu, Lucian Pop, Daniel Radavoi

المصدر: Cancer Diagn Progn

مصطلحات موضوعية: Computer science, Case Report, Identification (biology), Case presentation, Computational biology, New variant, Gene

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3b06a886ac73c788ef93dcff77ded291Test
https://doi.org/10.21873/cdp.10029Test

المؤلفون: Iasi Pharmacy, Radu Ursu, Agnes Katalin Lackner, Viorica Radoi, Andrei Kozma, Bucharest Balneoclimatology, Doriana Agop Forna, Horia Lăzărescu, Laurentiu Camil Bohiltea, Bucharest Pharmacy

المصدر: Romanian Journal of Stomatology, Vol 65, Iss 2, Pp 97-100 (2019)

مصطلحات موضوعية: Genetics, business.industry, Genetic counseling, enamel, RK1-715, amelogenesis imperfecta, Industrial and Manufacturing Engineering, stomatognathic diseases, stomatognathic system, Dentistry, Medicine, genetics, business

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::89161a8371fdb4b26cf15240c2ea1a92Test
https://doi.org/10.37897/rjs.2019.2.1Test

المؤلفون: Cristian Toma, Viorel Jinga, Paul D. Iordache, Titus Valentin Grigorean, Dumitru Cristinel Badiu, George Daniel Radavoi, Viorica Radoi, Radu Ursu, Mihaela Mandu, Cristian Sorin Sima, Bogdan Braticevici, Razvan Danau, Stefan Rascu

المصدر: ROMANIAN BIOTECHNOLOGICAL LETTERS. 24:100-107

مصطلحات موضوعية: Oncology, medicine.medical_specialty, education.field_of_study, business.industry, Romanian, Population, medicine.disease, Applied Microbiology and Biotechnology, language.human_language, Prostate cancer, Internal medicine, Genetics, medicine, language, Genetic risk, education, business, Agronomy and Crop Science, Biotechnology

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_________::53cad11a7aa64283b0a48f1c7792cdd9Test
https://doi.org/10.25083/rbl/24.1/100.107Test

المؤلفون: Bjarni Gunnarsson, Viorel Jinga, Angelica Voinoiu, Hrefna Johannsdottir, Stefan Rascu, Stefania Benonisdottir, Violeta Calota, Sorin Cristian Sima, Jon G. Jonasson, Razvan Danau, Dana Mates, Viorica Radoi, Daniel Badescu, Radu Ursu, Camelia Nicolae, Gudny A. Arnadottir, Cătălin Alexandru Staicu, Bjarni V. Halldorsson, Thorunn Rafnar, Paul D. Iordache, Aslaug Jonasdottir, Asgeir Sigurdsson, Kari Stefansson, Mihai Dobra, Irma Eva Csiki, Hannes P. Eggertsson, Sigrun Kristjansdottir, Ioan Nicolae Mates, Mariana Jinga, Louise le Roux, Andrei Manolescu, Brynjar O. Jensson, Nicoleta Suciu, Daniel Radavoi, Gabriel Rosoga, Patrick Sulem

المساهمون: Læknadeild (HÍ), Faculty of Medicine (UI), Tækni- og verkfræðideild (HR), School of Science and Engineering (RU), Heilbrigðisvísindasvið (HÍ), School of Health Sciences (UI), Háskólinn í Reykjavík, Reykjavik University, Háskóli Íslands, University of Iceland

المصدر: Journal of Cellular and Molecular Medicine

مصطلحات موضوعية: Male, 0301 basic medicine, Rúmenía, DNA Mismatch Repair, DNA Glycosylases, Risk Factors, PMS2, Mismatch Repair Endonuclease PMS2, Genetics, education.field_of_study, Middle Aged, Lynch syndrome, 3. Good health, DNA-Binding Proteins, MutS Homolog 2 Protein, Adenomatous Polyposis Coli, Molecular Medicine, Female, Original Article, MutL Protein Homolog 1, Adult, congenital, hereditary, and neonatal diseases and abnormalities, Lynch heilkenni, Population, Biology, MLH1, Familial adenomatous polyposis, 03 medical and health sciences, MUTYH, medicine, Humans, Genetic Predisposition to Disease, MLH1,MSH2,MSH6, MUTYH,PMS2, education, neoplasms, Aged, Endaþarmskrabbamein, Romania, nutritional and metabolic diseases, Original Articles, Cell Biology, DNA Methylation, medicine.disease, Colorectal Neoplasms, Hereditary Nonpolyposis, Colorectal cancer, digestive system diseases, MSH6, 030104 developmental biology, MSH2, Mutation

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::beb71a9cd3010c7f038a6df677219bc6Test
https://doi.org/10.1111/jcmm.13881Test

المؤلفون: Thorunn Rafnar, Viorel Jinga, Stefan Rascu, Viorica Radoi, Daniel Badescu, Stefania Benonisdottir, Bjarni V. Halldorsson, Angelica Voinoiu, Radu Ursu, Hannes P. Eggertsson, Bjarni Gunnarsson, Paul D. Iordache, Razvan Danau, Cătălin Alexandru Staicu, Irma Eva Csiki, Mariana Jinga, Violeta Calota, Dana Mates, Nicoleta Suciu, Patrick Sulem, Daniel Radavoi, Gabriel Rosoga, Kari Stefansson, Sorin Cristian Sima, Andrei Manolescu, Júlíus Guðmundsson

المساهمون: Læknadeild (HÍ), Faculty of Medicine (UI), Tækni- og verkfræðideild (HR), School of Science and Engineering (RU), School of Health Sciences (UI), Heilbrigðisvísindasvið (HÍ), Háskólinn í Reykjavík, Reykjavik University, Háskóli Íslands, University of Iceland

المصدر: Journal of Cellular and Molecular Medicine

مصطلحات موضوعية: 0301 basic medicine, Male, Erfðagreining, Genome-wide association study, unscreened population, Unscreened population, Genome-wide association studies, Prostate cancer, Gene Frequency, GWAS, genome‐wide association study, Oligonucleotide Array Sequence Analysis, Genetics, Prostate cancer risk, Aged, 80 and over, education.field_of_study, Middle Aged, prostate cancer, 3. Good health, Molecular Medicine, Population study, Original Article, Risk, Population, Single-nucleotide polymorphism, Blöðruhálskirtilskrabbamein, Biology, Polymorphism, Single Nucleotide, 03 medical and health sciences, medicine, Biomarkers, Tumor, SNP, Erfðafræði, Humans, Genetic Predisposition to Disease, 1000 Genomes Project, education, Alleles, Aged, Neoplasm Staging, Romania, Genome, Human, Gene Expression Profiling, Prostatic Neoplasms, Cell Biology, Rannsóknir, Original Articles, Prostate-Specific Antigen, medicine.disease, 030104 developmental biology, Genetic Loci, Case-Control Studies, Genome-Wide Association Study

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e347f6d1ee2040725e35a42a4f8dc28dTest
http://europepmc.org/articles/PMC5824401Test