المؤلفون: Stanley, KE, Jatsenko, T, Tuveri, S, Sudhakaran, D, Lannoo, L, Van Calsteren, K, de Borre, M, Van Parijs, I, Van Coillie, L, Van Den Bogaert, K, Toledo, RD, Lenaerts, L, Tejpar, S, Punie, K, Rengifo, LY, Vandenberghe, P, Thienpont, B, Vermeesch, JR

المصدر: Nature communications. 15(1):2220

مصطلحات موضوعية: Medicin och hälsovetenskap

URL الوصول: http://kipublications.ki.se/Default.aspx?queryparsed=id:155355740

المؤلفون: Bueno, MI, Rengifo, LY, Vergara, AP

المصدر: Repositorio UN
Universidad Nacional de Colombia
instacron:Universidad Nacional de Colombia

مصطلحات موضوعية: Citogenética, Bandeamiento cromosómico

وصف الملف: application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::36d2d214922d9a119127f0d98b15fa70
https://repositorio.unal.edu.co/handle/unal/74456

المؤلفون: Rengifo LY; Center for Human Genetics, KU Leuven, Leuven, Belgium., Smits S; Center for Human Genetics, KU Leuven, Leuven, Belgium., Boeckx N; Laboratory Medicine, University Hospitals Leuven, Leuven, Belgium.; Department of Oncology, KU Leuven, Leuven, Belgium., Michaux L; Center for Human Genetics, KU Leuven, Leuven, Belgium.; Center for Human Genetics, University Hospitals Leuven, Leuven, Belgium., Vandenberghe P; Center for Human Genetics, KU Leuven, Leuven, Belgium.; Department of Hematology, University Hospitals Leuven, Leuven, Belgium., Dewaele B; Center for Human Genetics, KU Leuven, Leuven, Belgium.; Center for Human Genetics, University Hospitals Leuven, Leuven, Belgium.

المصدر: Genes, chromosomes & cancer [Genes Chromosomes Cancer] 2023 Nov; Vol. 62 (11), pp. 663-671. Date of Electronic Publication: 2023 Jun 09.

نوع المنشور: Journal Article

بيانات الدورية: Publisher: Wiley-Liss Country of Publication: United States NLM ID: 9007329 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1098-2264 (Electronic) Linking ISSN: 10452257 NLM ISO Abbreviation: Genes Chromosomes Cancer Subsets: MEDLINE

مواضيع طبية MeSH: Neoplasms* , Myelodysplastic Syndromes*/genetics , Myelodysplastic Syndromes*/diagnosis, Humans ; Bone Marrow ; Retrospective Studies ; Cytogenetic Analysis/methods ; Whole Genome Sequencing

المؤلفون: Rengifo LY; Department of Human Genetics, KU Leuven, Leuven, Belgium. Electronic address: laurayissel.rengifocoronel@kuleuven.be., Smits S; Department of Human Genetics, KU Leuven, Leuven, Belgium., Buedts L; Department of Human Genetics, KU Leuven, Leuven, Belgium., Delforge M; Department of Hematology, University Hospitals Leuven, Leuven, Belgium., Dehaspe L; Center for Human Genetics, University Hospitals Leuven, Leuven, Belgium., Tousseyn T; Laboratory for Translational Cell and Tissue Research, Department of Imaging and Pathology, KU Leuven, Leuven, Belgium., Boeckx N; Laboratory Medicine, University Hospitals Leuven, Leuven, Belgium; Department of Oncology, KU Leuven, Leuven, Belgium., Lehnert S; Genomics Core, KU Leuven, Leuven, Belgium., Michaux L; Center for Human Genetics, University Hospitals Leuven, Leuven, Belgium., Vermeesch JR; Center for Human Genetics, University Hospitals Leuven, Leuven, Belgium., Vandenberghe P; Department of Human Genetics, KU Leuven, Leuven, Belgium; Department of Hematology, University Hospitals Leuven, Leuven, Belgium., Dewaele B; Center for Human Genetics, University Hospitals Leuven, Leuven, Belgium. Electronic address: barbara.dewaele@uzleuven.be.

المصدر: Cancer treatment and research communications [Cancer Treat Res Commun] 2021; Vol. 28, pp. 100380. Date of Electronic Publication: 2021 Apr 25.

نوع المنشور: Journal Article; Research Support, Non-U.S. Gov't

بيانات الدورية: Publisher: Elsevier Country of Publication: England NLM ID: 101694651 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 2468-2942 (Electronic) Linking ISSN: 24682942 NLM ISO Abbreviation: Cancer Treat Res Commun Subsets: MEDLINE

مواضيع طبية MeSH: Cell-Free Nucleic Acids* , Whole Genome Sequencing*, Multiple Myeloma/*genetics, Bone Marrow ; DNA Copy Number Variations ; Humans ; In Situ Hybridization, Fluorescence ; Plasma Cells

المؤلفون: Rengifo LY; Center for Human Genetics University Hospitals Leuven Leuven Belgium., Michaux L; Center for Human Genetics University Hospitals Leuven Leuven Belgium., Maertens J; Department of Microbiology and Immunology KU Leuven Leuven Belgium.; Department of Hematology University Hospitals Leuven Leuven Belgium., Tousseyn T; Department of Pathology University Hospitals Leuven Leuven Belgium., Lenaerts L; Department of Oncology KU Leuven Leuven Belgium., Vermeesch JR; Center for Human Genetics University Hospitals Leuven Leuven Belgium., Vandenberghe P; Center for Human Genetics University Hospitals Leuven Leuven Belgium.; Department of Hematology University Hospitals Leuven Leuven Belgium., Dewaele B; Center for Human Genetics University Hospitals Leuven Leuven Belgium.

المصدر: Clinical case reports [Clin Case Rep] 2020 Jun 20; Vol. 8 (10), pp. 1924-1927. Date of Electronic Publication: 2020 Jun 20 (Print Publication: 2020).

نوع المنشور: Case Reports

بيانات الدورية: Publisher: John Wiley & Sons Country of Publication: England NLM ID: 101620385 Publication Model: eCollection Cited Medium: Print ISSN: 2050-0904 (Print) Linking ISSN: 20500904 NLM ISO Abbreviation: Clin Case Rep Subsets: PubMed not MEDLINE

المؤلفون: Vervoort L; Department of Human Genetics, KU Leuven, Leuven, Belgium., Demaerel W; Department of Human Genetics, KU Leuven, Leuven, Belgium., Rengifo LY; Department of Human Genetics, KU Leuven, Leuven, Belgium., Odrzywolski A; Department of Human Genetics, KU Leuven, Leuven, Belgium.; Department of Biochemistry and Molecular Biology, Medical University of Lublin, Lublin, Poland., Vergaelen E; Department of Human Genetics, KU Leuven, Leuven, Belgium., Hestand MS; Department of Human Genetics, KU Leuven, Leuven, Belgium.; Division of Human Genetics, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, USA.; Department of Pediatrics, University of Cincinnati, Cincinnati, OH, USA., Breckpot J; Department of Human Genetics, KU Leuven, Leuven, Belgium., Devriendt K; Department of Human Genetics, KU Leuven, Leuven, Belgium., Swillen A; Department of Human Genetics, KU Leuven, Leuven, Belgium., McDonald-McGinn DM; Division of Human Genetics, Children's Hospital of Philadelphia, Philadelphia, PA, USA.; Department of Pediatrics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA., Fiksinski AM; Brain Center Rudolf Magnus, University Medical Center Utrecht, Utrecht, The Netherlands.; The Dalglish Family 22q Clinic and Centre for Addiction and Mental Health, Toronto, ON, Canada., Zinkstok JR; Brain Center Rudolf Magnus, University Medical Center Utrecht, Utrecht, The Netherlands., Morrow BE; Department of Genetics, Albert Einstein College of Medicine, Bronx, NY, USA., Heung T; The Dalglish Family 22q Clinic and Centre for Addiction and Mental Health, Toronto, ON, Canada.; Department of Psychiatry, University of Toronto, Toronto, ON, Canada., Vorstman JAS; Brain Center Rudolf Magnus, University Medical Center Utrecht, Utrecht, The Netherlands.; The Dalglish Family 22q Clinic and Centre for Addiction and Mental Health, Toronto, ON, Canada., Bassett AS; The Dalglish Family 22q Clinic and Centre for Addiction and Mental Health, Toronto, ON, Canada.; Department of Psychiatry, University of Toronto, Toronto, ON, Canada., Chow EWC; Department of Psychiatry, University of Toronto, Toronto, ON, Canada.; Clinical Genetics Service, Centre for Addiction and Mental Health, Toronto, ON, Canada., Shashi V; Department of Pediatrics, Duke University School of Medicine, Durham, NC, USA., Vermeesch JR; Department of Human Genetics, KU Leuven, Leuven, Belgium.

مؤلفون مشاركون: International 22q11.2 Brain, Behavior Consortium

المصدر: Human molecular genetics [Hum Mol Genet] 2019 Nov 15; Vol. 28 (22), pp. 3724-3733.

نوع المنشور: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't

بيانات الدورية: Publisher: IRL Press at Oxford University Press Country of Publication: England NLM ID: 9208958 Publication Model: Print Cited Medium: Internet ISSN: 1460-2083 (Electronic) Linking ISSN: 09646906 NLM ISO Abbreviation: Hum Mol Genet Subsets: MEDLINE

مواضيع طبية MeSH: DiGeorge Syndrome/*genetics , DiGeorge Syndrome/*metabolism , Homologous Recombination/*genetics, Adult ; Alleles ; Chromosome Breakpoints ; Chromosome Deletion ; Chromosome Inversion/genetics ; Chromosome Mapping/methods ; Chromosomes/genetics ; Chromosomes, Human, Pair 22/genetics ; Female ; Humans ; In Situ Hybridization, Fluorescence/methods ; Male ; Segmental Duplications, Genomic/genetics ; Whole Genome Sequencing/methods

المؤلفون: Botero S; Departamento de Ciencias Biológicas, Universidad de los Andes, Bogotá, Colombia. sbotero@rockefeller.edu, Rengifo LY, Bueno ML, Stevenson PR

المصدر: American journal of primatology [Am J Primatol] 2010 Dec; Vol. 72 (12), pp. 1131-40.

نوع المنشور: Journal Article; Research Support, Non-U.S. Gov't

بيانات الدورية: Publisher: Wiley-Blackwell Country of Publication: United States NLM ID: 8108949 Publication Model: Print Cited Medium: Internet ISSN: 1098-2345 (Electronic) Linking ISSN: 02752565 NLM ISO Abbreviation: Am J Primatol Subsets: MEDLINE

مواضيع طبية MeSH: Phylogeny* , Trees*, Atelinae/*genetics, Animals ; Atelinae/classification ; Base Sequence ; Bayes Theorem ; Colombia ; DNA Primers/genetics ; DNA, Mitochondrial/genetics ; Genetics, Population ; Karyotyping ; Models, Genetic ; Molecular Sequence Data ; Population Dynamics ; Sequence Analysis, DNA ; Species Specificity