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1
المؤلفون: Shu Liu, Nuan Chen, Weihong Zeng, Haimei OuYang, Xunjie Xie, Sisi Wei, Zhiqing Wang, Jinqun Liang, Liying Chen, Jianhui Jiang
المصدر: Cytogenetic and Genome Research. 154:201-208
مصطلحات موضوعية: Adult, Male, 0301 basic medicine, Gray matter heterotopia, Microcephaly, Pathology, medicine.medical_specialty, Candidate gene, Developmental Disabilities, Ring chromosome, Biology, 03 medical and health sciences, 0302 clinical medicine, Intellectual Disability, Cytogenetic Abnormality, Intellectual disability, Genetics, medicine, Humans, Ring Chromosomes, Gray Matter, Child, Molecular Biology, Genetics (clinical), 10 year follow up, Infant, Karyotype, Middle Aged, medicine.disease, 030104 developmental biology, Child, Preschool, Face, Chromosomes, Human, Pair 6, Female, 030217 neurology & neurosurgery, Follow-Up Studies
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::20db7deed22d6effbfddbc3c04ab040cTest
https://doi.org/10.1159/000488692Test -
2
المؤلفون: E. Engels, Soyhan Bagci, Annette M. Müller, Peter Bartmann, Heiko Reutter, E. Wohlleber, A.L. Berner, Ruthild G. Weber
المصدر: Cytogenetic and Genome Research. 136:308-313
مصطلحات موضوعية: Adult, Male, Infertility, Pediatrics, medicine.medical_specialty, Monosomy, Chromosomes, Human, Pair 20, Trisomy, Chromosomal translocation, Biology, Familial translocation, Translocation, Genetic, Chromosome Painting, Miscarriage, Pregnancy, Genetics, medicine, Humans, Abnormalities, Multiple, Molecular Biology, Genetics (clinical), Partial Trisomy, Infant, Karyotype, medicine.disease, Chromosome Banding, Pedigree, Phenotype, Karyotyping, Chromosomes, Human, Pair 6, Female, Chromosome Deletion
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::aeef29149f46e7a69008db432b495f08Test
https://doi.org/10.1159/000337019Test -
3
المؤلفون: Z. Zmitkova, Zdenek Sedlacek, Miroslava Hancarova, Zuzana Zemanova, D Raskova, Y Tan, D Novotna, Alena Puchmajerová, Marketa Vlckova, Jana Drabova, M Trkova
المصدر: Cytogenetic and Genome Research; Vol 136
مصطلحات موضوعية: Male, Marker chromosome, Karyotype, Biology, 03 medical and health sciences, Centromere, Genetics, Humans, Molecular Biology, Gene, Genetic Association Studies, In Situ Hybridization, Fluorescence, Genetics (clinical), 030304 developmental biology, Comparative Genomic Hybridization, 0303 health sciences, 030305 genetics & heredity, Breakpoint, Infant, Chromosome, Phenotype, Molecular biology, Chromosome Banding, Child, Preschool, Chromosomes, Human, Pair 6, Female, Chromosome Deletion, Comparative genomic hybridization
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d329035bb6f304cc807d0d03bab965faTest
https://doi.org/10.1159/000334709Test -
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المؤلفون: S. Selvarajah, Maisa Yoshimoto, Paul S. Thorner, Maria Zielenska, Olga Ludkovski, Paul C. Park, Jane Bayani, Georges Maire, Jeremy A. Squire
المصدر: Cytogenetic and Genome Research. 122:5-15
مصطلحات موضوعية: Male, musculoskeletal diseases, Chromosomes, Artificial, Bacterial, Adolescent, Gene Dosage, High resolution, Bone Neoplasms, Biology, Chromosomal Instability, Chromosome instability, Genetics, medicine, Humans, Child, Interphase, Molecular Biology, In Situ Hybridization, Fluorescence, Genetics (clinical), Oligonucleotide Array Sequence Analysis, Osteosarcoma, Karyotype, Prognosis, medicine.disease, Molecular biology, Karyotyping, Fish
, Chromosomes, Human, Pair 6, Female, Virtual karyotype, Chromosomes, Human, Pair 17, Chromosomes, Human, Pair 8, Comparative genomic hybridization الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d6f3c4578654ace184b72d1bbf5ce8f4Test
https://doi.org/10.1159/000151310Test -
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المؤلفون: Jörg Weimer, Walter Jonat, Ute Wiedemann, Norbert Arnold, U.R. Heinrich, M. Cohen
المصدر: Cytogenetic and Genome Research. 114:235-239
مصطلحات موضوعية: media_common.quotation_subject, Mothers, Chromosomal translocation, Allelic Imbalance, Biology, Translocation, Genetic, Genetics, Humans, Molecular Biology, In Situ Hybridization, Fluorescence, Genetics (clinical), Microdissection, media_common, Chromosome Aberrations, Daughter, Chromosomes, Human, Pair 11, Dissection, Chromosome Mapping, Telomere, Phenotype, Molecular biology, Fish
, Chromosomes, Human, Pair 6, Female, Dandy-Walker variant الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::89a1677987ff867f710156b1b645671fTest
https://doi.org/10.1159/000094206Test -
6
المؤلفون: Hildegard Kehrer-Sawatzki, H. Röck, W. Krone, A. Siegel, H. Götz
المصدر: Cytogenetic and Genome Research. 86:28-33
مصطلحات موضوعية: Adult, Male, Monosomy, Time Factors, Loss of Heterozygosity, Stimulation, Biology, Fibroblast growth factor, Cell Line, Nondisjunction, Genetic, Dosage Compensation, Genetic, Genetics, medicine, Humans, Selection, Genetic, Child, Fibroblast, Molecular Biology, Alleles, In Situ Hybridization, Fluorescence, Genetics (clinical), Fibroblast growth factor receptor 2, Chromosome Breakage, Fibroblasts, FGF1, medicine.disease, Molecular biology, In vitro, Clone Cells, medicine.anatomical_structure, Receptors, Androgen, Cell culture, Fibroblast Growth Factor 1, Chromosomes, Human, Pair 6, Female, Fibroblast Growth Factor 2, Cell Division, Microsatellite Repeats
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f9a65faa17f504c6f10cef79897102e5Test
https://doi.org/10.1159/000015424Test -
7
المؤلفون: Emilio Garcia, Reinhilde Thoelen, M. Aly, Koenraad Devriendt, W.J.M. Van de Ven, Peter M.A. Groenen, J. P. Fryns, Eric F.P.M. Schoenmakers
المصدر: Cytogenetic and Genome Research. 75:210-215
مصطلحات موضوعية: Adult, Chromosome Breakpoints, Chromosome Disorders, Chromosomal translocation, Locus (genetics), Hydronephrosis, Biology, Polymerase Chain Reaction, Oligohydramnios, Translocation, Genetic, Gene mapping, Pregnancy, Chromosome 19, Genetics, medicine, Humans, Kidney Pelvis, Lung, Molecular Biology, In Situ Hybridization, Fluorescence, Genetics (clinical), Chromosome Aberrations, Polycystic Kidney Diseases, medicine.diagnostic_test, Breakpoint, DNA, Fibroblasts, Cosmids, Fetal Diseases, Cosmid, Chromosomes, Human, Pair 6, Female, Ureter, Chromosomes, Human, Pair 19, Ureteral Obstruction, Fluorescence in situ hybridization
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::718d0c0a91b4361c7412109efa277a29Test
https://doi.org/10.1159/000134485Test -
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المؤلفون: Marine Guillaud-Bataille, R. Berger, Alain Bernheim, H. Waxin, S. Toujani, C. Richon, P. Dessen
المصدر: Cytogenetic and genome research. 119(3-4)
مصطلحات موضوعية: Genetics, Daughter, media_common.quotation_subject, Breakpoint, Gene Dosage, Chromosome Breakage, DNA, Biology, Familial translocation, Translocation, Genetic, Cell Line, Array-Based Comparative Genomic Hybridization, Chromosomes, Human, Pair 2, Karyotyping, Humans, Chromosomes, Human, Pair 6, Female, DNA Probes, Molecular Biology, Genetics (clinical), In Situ Hybridization, Fluorescence, media_common, Oligonucleotide Array Sequence Analysis
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::efa3f98b3855412963781aefa7569486Test
https://pubmed.ncbi.nlm.nih.gov/18253027Test -
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المؤلفون: Michael B. Petersen, Yolanda Gyftodimou, Maria Grigoriadou, Haris Kokotas, Efi Pandelia, Catherine Sarri, Kristin Mrasek, S. Kalogirou, Anja Weise
المصدر: Cytogenetic and genome research. 114(3-4)
مصطلحات موضوعية: Genetic Markers, Heart Defects, Congenital, Marker chromosome, Biology, Craniofacial Abnormalities, Gene duplication, Genetics, medicine, Humans, Supernumerary, Abnormalities, Multiple, Child, Molecular Biology, Small supernumerary marker chromosome, Genetics (clinical), In Situ Hybridization, Fluorescence, Chromosome Aberrations, medicine.diagnostic_test, Chromosome, Chromosome Mapping, Karyotype, medicine.disease, Uniparental disomy, Karyotyping, Chromosomes, Human, Pair 6, Female, Fluorescence in situ hybridization
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::51e39ae587158cdee29a0f332f5219dbTest
https://pubmed.ncbi.nlm.nih.gov/16954675Test -
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المؤلفون: T H, Vu, R L, Jirtle, A R, Hoffman
المصدر: Cytogenetic and genome research. 113(1-4)
مصطلحات موضوعية: Male, Exons, DNA Methylation, Receptor, IGF Type 2, Evolution, Molecular, Genomic Imprinting, Mice, Gene Expression Regulation, Species Specificity, Vertebrates, Animals, Humans, Chromosomes, Human, Pair 6, Female
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=pmid________::7bb911973168312dca618124213bb865Test
https://pubmed.ncbi.nlm.nih.gov/16575181Test