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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 -
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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 -
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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: 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