المؤلفون: Orsetta Zuffardi, Stavros Sifakis, George Kitsos, Michael B. Petersen, Martina Merkas, Konstantinos Kefalas, Sotirios Sotiriou, Georgios Aperis, Loretta Thomaidis, Emmanouil Manolakos, Ioannis Papoulidis, Annalisa Vetro, Thomas Liehr

المصدر: American Journal of Medical Genetics Part A. 155:1476-1482

مصطلحات موضوعية: Pathology, medicine.medical_specialty, Microcephaly, Intellectual Disability/genetics/*pathology, media_common.quotation_subject, Abnormalities, Multiple/genetics/*pathology, In situ hybridization, Central nervous system disease, Chromosomes, Human, Pair 2/*genetics, Intellectual Disability, Genetics, medicine, Humans, Abnormalities, Multiple, Girl, In Situ Hybridization, Fluorescence, Genetics (clinical), media_common, Comparative Genomic Hybridization, business.industry, Phenotype, Karyotype, Chromosome Deletion, medicine.disease, Developmental disorder, Child, Preschool, Chromosomes, Human, Pair 2, Karyotyping, Female, Microcephaly/genetics/*pathology, business, Comparative genomic hybridization

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::64f1246508e0b8b45c78a9eb7d6b9bf0
https://doi.org/10.1002/ajmg.a.33981

المؤلفون: Anamaria Štambuk, Maja Šrut, Goran Klobučar, Luka Traven, Želimira Cvetković, Martina Merkas, Ivana Husnjak

المصدر: Environmental Pollution. 159:841-849

مصطلحات موضوعية: Eisenia fetida, Pentachlorophenol, Croatia, Health, Toxicology and Mutagenesis, 010501 environmental sciences, Toxicology, medicine.disease_cause, 01 natural sciences, chemistry.chemical_compound, 11. Sustainability, medicine, Animals, Soil Pollutants, Oligochaeta, Vehicle Emissions, 0105 earth and related environmental sciences, biology, Copper toxicity, Earthworm, 04 agricultural and veterinary sciences, General Medicine, medicine.disease, biology.organism_classification, Pollution, Soil contamination, Comet assay, DNA damage, NRRT assay, coelomocytes, Aporrectodea caliginosa, chemistry, Neutral Red, Environmental chemistry, 040103 agronomy & agriculture, 0401 agriculture, forestry, and fisheries, Biological Assay, Comet Assay, Copper, Genotoxicity, Cadmium, Environmental Monitoring

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a8c766ab05f4ce98a3870a0ddca31556
https://doi.org/10.1016/j.envpol.2011.01.009

المؤلفون: Elisabeth Ewers, Kristin Mrasek, Nadezda Kosyakova, Anja Weise, Martina Merkas, Thomas Liehr, Lukrecija Brecevic, Ahmed B. Hamid, Tatyana V. Karamysheva

المصدر: Current Genomics

مصطلحات موضوعية: Genetics, Chromosome number, Screening test, business.industry, Genetic counseling, Karyotype, small supernumerary marker chromosomes (sSMC), Article, mosaic, genotype-phenotype correlation, Somatic mosaicism, Chromosome instability, Centromere, Medicine, Supernumerary, business, Mosaic, Genetics (clinical)

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6dac920f09c0c27e13fd93cf15fedeb6
https://doi.org/10.2174/138920210793176029

المؤلفون: Monika Ziegler, G.R. Pilic, Martina Merkas, Elisabeth Ewers, S.B. Niksic, Thomas Liehr, V.I. Deretic

المصدر: Balkan Journal of Medical Genetics, Vol 13, Iss 1, Pp 55-58 (2010)

مصطلحات موضوعية: Genetics, Partial Trisomy, down syndrome, medicine.diagnostic_test, Healthy subjects, Karyotype, small supernumerary marker chromosome (ssmc), Biology, QH426-470, medicine.disease, medicine, Fish , partial trisomy 18p, small supernumerary marker chromosome (sSMC), Partial trisomy 18p, Down syndrome, Trisomy, Small supernumerary marker chromosome, Genetics (clinical), Fluorescence in situ hybridization

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5300884e3644693929ffc481e07018f3
https://doaj.org/article/6baee4dd10984eebbf6ac1c8c5b9a086

المؤلفون: Emel Ergul, Martina Merkas, A Polityko, Gisela Reising-Ackermann, Marianne Volleth, Anna I. Kulpanovich, Marcelo de Bello Cioffi, Markus Stumm, Alla Frolova, Isabella Simonyan, Thomas Liehr, Samarth Bhatt, Monika Ziegler, Hasmik Mkrtchyan, Isolde Schreyer, Katharina Kreskowski, Thomas Martin, Ani Grigorian, Laura R. Rodríguez, Lukretija Brecevic, Evgenia Jaroshevich, Tatiana Egorova, Svetlana G. Vorsanova, Nadezda Kosyakova, Heike Nelle, Irina Naumchik, Natalia Shorokh, Anja Weise, Marina Manvelyan, Rouben Aroutiounian, Ali Sazci, Rolf-Dieter Wegner

المصدر: Molecular Cytogenetics

مصطلحات موضوعية: Breakpoints, medicine.medical_specialty, Heterochromatin, Western Europe, Chromosome 9, Eastern Europe, Biology, Biochemistry, Dicentric chromosome, Research based, medicine, Genetics, Genetics(clinical), Heteromorphism, Molecular Biology, Genetics (clinical), Biochemistry, medical, Research, Biochemistry (medical), Breakpoint, Cytogenetics, heteromorphism, breakpoints, Human genetics, Western europe, Molecular Medicine

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b88e7e616715b34c4787c77d0df549f9
https://pubmed.ncbi.nlm.nih.gov/23547710

المؤلفون: Iris Bartels, Barbara Zoll, Nadezda Kosyakova, F. von Eggeling, Ahmed B. Hamid, Nicole Posorski, Thomas Liehr, Kristin Mrasek, Martina Merkas, Anja Weise, Elisabeth Ewers

مصطلحات موضوعية: Genetics, Chromosome Aberrations, 0303 health sciences, Chromosome engineering, 4p14, Duplication, Small supernumerary marker chromosome, Unbalanced chromosomal abnormalities, Autosome, 030302 biochemistry & molecular biology, Chromosomal rearrangement, Biology, 03 medical and health sciences, Chromosome 4, Karyotyping, Chromosomal region, Chromosomal polymorphism, Humans, Chromosomes, Human, Pair 4, Molecular Biology, Genetics (clinical), In Situ Hybridization, Fluorescence, 030304 developmental biology, Comparative genomic hybridization

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e81255bedc8ab76eab030fa0ca4c0993
http://resolver.sub.uni-goettingen.de/purl?gs-1/8160

المؤلفون: Nikolai Rubtsov, Martina Merkas, Ahmed B. Hamid, Thomas Liehr, Alma Küchler, Isolde Schreyer, Ferdinand von Eggeling, Raimund Fahsold, Jasen Anderson, Nadezda Kosyakova, Kristin Mrasek, Julia Hentschel, Elisabeth Ewers, Heike Nelle, Anikó Ujfalusi, Anja Weise

مصطلحات موضوعية: Genetics, Cancer Research, Pathology, medicine.medical_specialty, Heterochromatin, small supernumerary marker chromosomes, fragile X-syndrome, unclear mental retardation, Orvostudományok, Biology, medicine.disease, Klinikai orvostudományok, Biochemistry, Phenotype, Uniparental disomy, Fragile X syndrome, Oncology, medicine, Molecular Medicine, Supernumerary, Clinical case, Genetic diagnosis, Molecular Biology, Small supernumerary marker chromosome

وصف الملف: application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c1c92d1ba50c42acbfef3d532589cb18

المؤلفون: Thomas Liehr, Tatyana Karamysheva, Martina Merkas, Lukrecija Brecevic, Ahmed B. Hamid, Elisabeth Ewers, Kristin Mrasek, Nadezda Kosyakova, Anja Weise

المساهمون: The Pennsylvania State University CiteSeerX Archives

المصدر: ftp://ftp.ncbi.nlm.nih.gov/pub/pmc/9e/6b/Curr_Genomics_2010_Sep_11(6)_432-439.tar.gz

مصطلحات موضوعية: Mosaic, small supernumerary marker chromosomes (sSMC, genotype-phenotype correlation. SMALL SUPERNUMERARY MARKER CHROMO

وصف الملف: application/zip

Relation: http://citeseerx.ist.psu.edu/viewdoc/summary?doi=10.1.1.292.2259

الاتاحة: http://citeseerx.ist.psu.edu/viewdoc/summary?doi=10.1.1.292.2259