يعرض 1 - 20 نتائج من 79 نتيجة بحث عن '"Froyen, Guido"', وقت الاستعلام: 0.41s تنقيح النتائج
  1. 1
    Patent
    Recombinant DNA-molecule complex for the expression of anti-human-interferon-gamma chimeric antibodies or antibody fragments
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  2. 2
    Conference
    Breakpoint cloning of aberrations on the X chromosome: identification of an unusual type of recombination that results in a dosage-dependent severity of the phenotype

    المؤلفون: Froyen, Guido, Bauters, Marijke, Vandewalle, Joke, Marynen, Peter

    Relation: Genomics Disorders meeting location:Hinxton, UK date:24-26 March 2010; https://lirias.kuleuven.be/handle/123456789/290788

    الاتاحة: https://lirias.kuleuven.be/handle/123456789/290788

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  3. 3
    Conference
    Poster session: Deficiency in nuclear RNA export factor 7 impairs hippocampal synaptic plasticity and spatial learning in the Morris water maze

    المؤلفون: Callaerts-Vegh, Zsuzsanna, Ahmed, Tariq, Balschun, Detlef, Roebroek, Anton, Froyen, Guido, D'Hooge, Rudi

    Relation: FENS abstract vol:5; FENS Forum of European Neuroscience edition:7 location:Amsterdam date:3 - 7 july 2010; FENS Abstr., vol.5, 115.17, 2010; https://lirias.kuleuven.be/handle/123456789/271752

    الاتاحة: https://lirias.kuleuven.be/handle/123456789/271752

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  4. 4
    Conference
    Development and validation of the 'chromosome X exon-specific array' that enables identification of copy number changes in genes of the X chromosome

    المؤلفون: Patsalis, P, Kousoulidou, L, Van Bokoven, H, Ropers, H, Chelly, J, Moraine, C, De Brouwer, A, Van Esch, Hilde, Froyen, Guido, Bashiardes, S

    Relation: Chromosome research vol:15 pages:227-227; 6th European Cytogenetics Conference location:Istanbul, Turkey date:Jul 07-10, 2007; https://lirias.kuleuven.be/handle/123456789/267882

    الاتاحة: https://lirias.kuleuven.be/handle/123456789/267882

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  5. 5
    Conference
    Detection of genomic copy number changes in patients with idiopathic mental retardation by high-resolution X-array-CGH: frequent increased gene dosage of known XLMR genes

    المؤلفون: Froyen, Guido, Van Esch, Hilde, Bauters, Marijke, Frints, SGM, Vermeesch, Joris, Devriendt, Koenraad, Fryns, Jean-Pierre, Marynen, Peter

    Relation: 13th International Workshop on Fragile X and X-linked Mental Retardation location:Venezia Lido, Italy date:3-6 October 2007; https://lirias.kuleuven.be/handle/123456789/262063

    الاتاحة: https://lirias.kuleuven.be/handle/123456789/262063

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  6. 6
    Conference
    Partial duplications of the ATRX-gene cause the ATR-X syndrome

    المؤلفون: Thienpont, Bernard, de Ravel, Thomy, Van Esch, Hilde, Van Schoubroeck, Dominique, Moerman, Philippe, Vermeesch, Joris, Fryns, Jean-Pierre, Froyen, Guido, Badens, C, Devriendt, Koenraad

    Relation: European Journal of Human Genetics vol:15 issue:suppl. 1 pages:42; European Human Genetics Conference 2007 location:Nice, France date:June 16-19, 2007; https://lirias.kuleuven.be/handle/123456789/262021

    الاتاحة: https://lirias.kuleuven.be/handle/123456789/262021

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  7. 7
    Conference
    Complex genomic architecture at xq28 results in duplication of mecp2 commonly found in a specific subset of MR patients

    المؤلفون: Bauters, Marijke, Van Esch, Hilde, Friez, M, Boespflug-Tanguy, Zenker, M, Vianna-Morgante, AM, Ignatius, J, Raynaud, M, Hollanders, K, Vandenreijt, K, Blanc, P, Moraine, C, Stevenson, R, Marynen, Peter, Fryns, Jean-Pierre, Schwartz, C, Froyen, Guido

    Relation: Cellular Oncology vol:29 issue:2 pages:108; 1st Marie Curie-Genome Architecture in Relation to Disease Meeting (MC-GARD) location:VU Univ Med Ctr, Amsterdam, Netherlands date:May 03-05, 2007; https://lirias.kuleuven.be/handle/123456789/261989

    الاتاحة: https://lirias.kuleuven.be/handle/123456789/261989

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  8. 8
    Conference
    Duplication and rearrangement of the MYB oncogene in T-cellacute lymphoblastic leukemia

    المؤلفون: Lahortiga, Idoya, Cauwelier, B, Dekeersmaecker, K, Van Vlieberghe, P, Graux, Carlos, Lambert, F, Mentens, N, Beverloo, H. B, Pieters, R, Speleman, F, Oderos, M. D, Bauters, Marijke, Froyen, Guido, Marynen, Peter, Vandenberghe, Peter, Wlodarska, Iwona, Cools, Jan

    Relation: Acta Clinica Belgica vol:62 issue:4 pages:252-252; Belgian Hematological Society (BHS) General meeting date:26-27 January 2007; https://lirias.kuleuven.be/handle/123456789/214721

    الاتاحة: https://lirias.kuleuven.be/handle/123456789/214721

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  9. 9
    Conference
    Duplication of the MYB oncogene in T-cell acute lymphoblastic leukemia

    المؤلفون: Lahortiga, Idoya, De Keersmaecker, Kim, Van Vlierberghe, P, Graux, Carlos, Cauwelier, B, Lambert, F, Mentens, N, Beverloo, H. B, Pieters, R, Speleman, F, Odero, M. D, Bauters, Marijke, Froyen, Guido, Marynen, Peter, Vandenberghe, Peter, Wlodarska, Iwona, Meijerink, J, Cools, Jan

    Relation: Haematologica vol:92 pages:164-164; Congress of the European-Hematology-Association edition:12 location:Vienna, Austria date:JUN 07-10, 2007; https://lirias.kuleuven.be/handle/123456789/214657

    الاتاحة: https://lirias.kuleuven.be/handle/123456789/214657

    View record in BASE Full Text Finder

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  10. 10
    Conference
    Detection of genomic copy number changes in patients with idiopathic mental retardation by highresolution X-array-CGH: frequent increased gene dosage of known .xlmr genes

    المؤلفون: Bauters, Marijke, Froyen, Guido, Van Esch, Hilde, Nevelsteen, Joke, Frints, SGM, Vermeesch, Joris, Devriendt, Koenraad, Fryns, Jean-Pierre, Marynen, Peter

    Relation: Cellular Oncology vol:29 issue:2 pages:133; 1st Marie Curie-Genome Architecture in Relation to Disease Meeting (MC-GARD) location:VU Univ Med Ctr, Amsterdam, Netherlands date:May 03-05, 2007; https://lirias.kuleuven.be/handle/123456789/261986

    الاتاحة: https://lirias.kuleuven.be/handle/123456789/261986

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  11. 11
    Conference
    Duplication of the MECP2 region is a frequent cause of severe mental retardation and neurological symptoms in males

    المؤلفون: Van Esch, Hilde, Bauters, Marijke, Ignatius, J, Raynaud, M, Hollanders, K, Lugtenberg, D, Bienvenu, T, Jensen, L, Moraine, C, Marynen, Peter, Froyen, Guido, Fryns, Jean-Pierre

    Relation: Genetic Counseling vol:17 issue:1 pages:119-120; 16th European Meeting on Dysmorphology location:Le Bischenberg, Strasbourg, France date:8-9 September 2005; https://lirias.kuleuven.be/handle/123456789/271662

    الاتاحة: https://lirias.kuleuven.be/handle/123456789/271662

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  12. 12
    Conference
    Duplications of the MECP2 region are commonly found in a specific subset of MR patients; towards a detailed genotype-phenotype correlation

    المؤلفون: Bauters, Marijke, Van Esch, Hilde, Friez, M, Boespflug-Tangui, O, Raynaud, M, Vianna-Morgante, M, Ignathius, J, Zenker, M, Vandenreijt, K, Blanc, P, Morraine, C, Stevenson, R, Marynen, Peter, Fryns, Jean-Pierre, Schwartz, C, Froyen, Guido

    Relation: European Journal of Human Genetics vol:14 issue:suppl 1 pages:90-90; European Human Genetics Conference 2006 in conjunction with the European Meeting on Psychosocial Aspects of Genetics location:Amsterdam, The Netherlands date:May 6-9, 2006; https://lirias.kuleuven.be/handle/123456789/271811

    الاتاحة: https://lirias.kuleuven.be/handle/123456789/271811

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  13. 13
    Conference
    Duplication de la region MECP2: naissance d’un nouveau syndrome de retard mental lié au chromosome X

    المؤلفون: Van Esch, Hilde, Bauters, Marijke, Ignatius, J, Raynaud, M, Moraine, C, Schwartz, C, Zenker, M, Vianna-Morgantte, A, Marynen, Peter, Fryns, Jean-Pierre, Froyen, Guido

    Relation: Médecine Sciences vol:22 issue:hors série n° 2 pages:14-14; 3èmes Assises de Génétique Humaine et Médicale location:Le Corum-Montpellier, France date:26-28 janvier 2006; https://lirias.kuleuven.be/handle/123456789/271674

    الاتاحة: https://lirias.kuleuven.be/handle/123456789/271674

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  14. 14
    Conference
    Deletion of the ophn1 gene in two brothers with severe mental retardation and neurological symptoms

    المؤلفون: Van Esch, Hilde, Froyen, Guido, Fryns, Jean-Pierre

    Relation: Genetic Counseling vol:17 issue:1 pages:119-119; 16th European Meeting on Dysmorphology location:Le Bischenberg, Strasbourg, France date:8-9 September 2005; https://lirias.kuleuven.be/handle/123456789/271612

    الاتاحة: https://lirias.kuleuven.be/handle/123456789/271612

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  15. 15
    Conference
    Duplications of the MECP2 gene are commonly found in a specific subset of patients with syndromal MR; towards a detailed genotype-phenotype correlation

    المؤلفون: Van Esch, Hilde, Bauters, Marijke, Friez, M, Boespflug-Tanguy, O, Raynaud, M, Vianna-Morgante, AM, Ignathius, J, Zenker, M, Blanc, P, Moraine, C, Stevenson, R, Marynen, Peter, Schkwartz, C, Froyen, Guido, Fryns, Jean-Pierre

    Relation: pages:14-14; 7th National conference for general practitioners and paediatricians with international participation location:Slanchev Briag, Bulgarije date:May 24-26, 2006; https://lirias.kuleuven.be/handle/123456789/271828

    الاتاحة: https://lirias.kuleuven.be/handle/123456789/271828

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  16. 16
    Conference
    Identification of new genes and genetic mechanisms in patients with X-linked mental retardation

    المؤلفون: Bauters, Marijke, Van Esch, Hilde, Frints, S, Van Hummelen, P, Marynen, Peter, Froyen, Guido

    Relation: Sixth Annual Meeting of the Belgian Society of Human Genetics location:Antwerp, Belgium date:February 17, 2006; https://lirias.kuleuven.be/handle/123456789/271772

    الاتاحة: https://lirias.kuleuven.be/handle/123456789/271772

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  17. 17
    Conference
    ArrayCGH analysis detects cryptic chromosomal aberrations in more than twenty percent of patients with idiopathic mental retardation and multiple congenital anomalies

    المؤلفون: Maas, NMC, Menten, B, Melotte, Cindy, Thienpont, Bernard, Buysse, K, Froyen, Guido, Marynen, Peter, De Paepe, A, Fryns, Jean-Pierre, Mortier, G, Devriendt, Koenraad, Vermeesch, Joris, Speleman, F

    Relation: Fifth Annual Meeting of the Belgian Society of Human Genetics location:Liège date:January 25, 2005; https://lirias.kuleuven.be/handle/123456789/263178

    الاتاحة: https://lirias.kuleuven.be/handle/123456789/263178

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  18. 18
    Conference
    ArrayCGH detects mosaics in similar to 4% of patients with MR/CA

    المؤلفون: Maas, N. M. C, Menten, B, Melotte, Cindy, Thienpont, Bernard, Buysse, K, Froyen, Guido, Marynen, Peter, De Paepe, A, Fryns, Jean-Pierre, Mortier, G, Devriendt, Koenraad, Vermeesch, Joris, Speleman, F

    Relation: Chromosome research vol:13 pages:202-203; 5th European Cytogenetics Conference (5th ECG) location:Madrid, Spain date:June 4-7, 2005; https://lirias.kuleuven.be/handle/123456789/261670

    الاتاحة: https://lirias.kuleuven.be/handle/123456789/261670

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  19. 19
    Conference
    Characterization of subtle copy number changes on the X chromosome identified in 7% of patients with X-linked mental retardation by high-resolution array-CGH

    المؤلفون: Bauters, Marijke, Van Esch, Hilde, Hollanders, K, Devriendt, Koenraad, Fryns, Jean-Pierre, Marynen, Peter, Froyen, Guido

    Relation: pages:6-6; Second Marie curie conference on ArrayCGH and Molecular Cytogenetics location:Bari, Italy date:October 20-22, 2005; https://lirias.kuleuven.be/handle/123456789/271096

    الاتاحة: https://lirias.kuleuven.be/handle/123456789/271096

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  20. 20
    Conference
    Screening of submicroscopic genomic aberrations in patients with X-linked mental retardation by high resolution array-CGH

    المؤلفون: Froyen, Guido, Van Esch, Hilde, Bauters, Marijke, Vermeesch, Joris, Vanhummelen, P, Fryns, Jean-Pierre, Devriendt, Koenraad, Marynen, Peter

    Relation: European Journal of Human Genetics vol:13 issue:suppl. 1 pages:89; European Human Genetics Conference 2005 location:Prague, Czech Republic date:May 7-10, 2005; https://lirias.kuleuven.be/handle/123456789/261636

    الاتاحة: https://lirias.kuleuven.be/handle/123456789/261636

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