يعرض 1 - 20 نتائج من 572 نتيجة بحث عن '"Gatt M."', وقت الاستعلام: 0.67s تنقيح النتائج
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    Report

    المؤلفون: Grandis, S., Ghirardini, V., Bocquet, S., Garrel, C., Mohr, J. J., Liu, A., Kluge, M., Kimmig, L., Reiprich, T. H., Alarcon, A., Amon, A., Artis, E., Bahar, Y. E., Balzer, F., Bechtol, K., Becker, M. R., Bernstein, G., Bulbul, E., Campos, A., Rosell, A. Carnero, Kind, M. Carrasco, Cawthon, R., Chang, C., Chen, R., Chiu, I., Choi, A., Clerc, N., Comparat, J., Cordero, J., Davis, C., Derose, J., Diehl, H. T., Dodelson, S., Doux, C., Drlica-Wagner, A., Eckert, K., Elvin-Poole, J., Everett, S., Ferte, A., Gatt, M., Giannini, G., Giles, P., Gruen, D., Gruendl, R. A., Harrison, I., Hartley, W. G., Herner, K., Huf, E. M., Kleinebreil, F., Kuropatkin, N., Leget, P. F., Maccrann, N., Mccullough, J., Merloni, A., Myles, J., Nandra, K., Navarro-Alsina, A., Okabe, N., Pacaud, F., Pandey, S., Prat, J., Predehl, P., Ramos, M., Raveri, M., Rollins, R. P., Roodman, A., Ross, A. J., Rykoff, E. S., Sanchez, C., Sanders, J., Schrabback, T., Secco, L. F., Seppi, R., Sevilla-Noarbe, I., Sheldon, E., Shin, T., Troxel, M., Tutusaus, I., Varga, T. N., Wu, H., Yanny, B., Yin, B., Zhang, X., Zhang, Y., Alves, O., Bhargava, S., Brooks, D., Burke, D. L., Carretero, J., Costanzi, M., da Costa, L. N., Pereira, M. E. S., De Vicente, J., Desai, S., Doel, P., Ferrero, I., Flaugher, B., Friedel, D., Frieman, J., García-Bellido, J., Gutierrez, G., Hinton, S. R., Hollowood, D. L., Honscheid, K., James, D. J., Jeffrey, N., Lahav, O., Lee, S., Marshall, J. L., Menanteau, F., Ogando, R. L. C., Pieres, A., Malagón, A. A. Plazas, Romer, A. K., Sanchez, E., Schubnell, M., Smith, M., Suchyta, E., Swanson, M. E. C., Tarle, G., Weaverdyck, N., Weller, J.

    المصدر: A&A 687, A178 (2024)

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    المصدر: European journal of human genetics, vol. 32, no. 4, pp. 407-412

    وصف الملف: application/pdf

    Relation: info:eu-repo/semantics/altIdentifier/pmid/38052905; info:eu-repo/semantics/altIdentifier/eissn/1476-5438; info:eu-repo/semantics/altIdentifier/urn/urn:nbn:ch:serval-BIB_D5E08218E6E95; https://serval.unil.ch/notice/serval:BIB_D5E08218E6E9; https://serval.unil.ch/resource/serval:BIB_D5E08218E6E9.P001/REF.pdf

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    Academic Journal

    المساهمون: Sozzoni, M., Ferrer Obiol, J., Formenti, G., Tigano, A., Paris, J. R., Balacco, J. R., Jain, N., Tilley, T., Collins, J., Sims, Y., Wood, J., Benowitz-Fredericks, Z. M., Field, K. A., Seyoum, E., Gatt, M. C., Leandri-Breton, D. -J., Nakajima, C., Whelan, S., Gianfranceschi, L., Hatch, S. A., Elliott, K. H., Shoji, A., Cecere, J. G., Jarvis, E. D., Pilastro, A., Rubolini, D.

    وصف الملف: ELETTRONICO

    Relation: info:eu-repo/semantics/altIdentifier/pmid/37590950; info:eu-repo/semantics/altIdentifier/wos/WOS:001055067300002; volume:15; issue:8; journal:GENOME BIOLOGY AND EVOLUTION; https://hdl.handle.net/11577/3494241; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85168796415; https://doi.org/10.1093/gbe/evad153

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    المصدر: American journal of medical genetics. Part A, vol. 191, no. 4, pp. 995-1006

    وصف الملف: application/pdf

    Relation: info:eu-repo/semantics/altIdentifier/pmid/36584346; info:eu-repo/semantics/altIdentifier/eissn/1552-4833; info:eu-repo/semantics/altIdentifier/urn/urn:nbn:ch:serval-BIB_B90F6ED045DA9; https://serval.unil.ch/notice/serval:BIB_B90F6ED045DA; https://serval.unil.ch/resource/serval:BIB_B90F6ED045DA.P001/REF.pdf

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    Academic Journal

    وصف الملف: application/pdf

    Relation: https://openaccess.sgul.ac.uk/id/eprint/115586/1/e071687.full.pdf; Claridge, H; Tan, J; Loane, M; Garne, E; Barisic, I; Cavero-Carbonell, C; Dias, C; Gatt, M; Jordan, S; Khoshnood, B; et al. Claridge, H; Tan, J; Loane, M; Garne, E; Barisic, I; Cavero-Carbonell, C; Dias, C; Gatt, M; Jordan, S; Khoshnood, B; Kiuru-Kuhlefelt, S; Klungsoyr, K; Mokoroa Carollo, O; Nelen, V; Neville, AJ; Pierini, A; Randrianaivo, H; Rissmann, A; Tucker, D; de Walle, H; Wertelecki, W; Morris, JK (2023) Ethics and legal requirements for data linkage in 14 European countries for children with congenital anomalies. BMJ Open, 13 (7). e071687. ISSN 2044-6055 https://doi.org/10.1136/bmjopen-2023-071687 SGUL Authors: Morris, Joan Katherine

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    المساهمون: Coi, A., Santoro, M., Pierini, A., Rankin, J., Glinianaia, S. V., Tan, J., Reid, A. -K., Garne, E., Loane, M., Given, J., Ballardini, E., Cavero-Carbonell, C., de Walle, H. E. K., Gatt, M., Garcia-Villodre, L., Gissler, M., Jordan, S., Kiuru-Kuhlefelt, S., Kjaer Urhoj, S., Klungsoyr, K., Lelong, N., Lutke, L. R., Neville, A. J., Rahshenas, M., Scanlon, I., Wellesley, D., Morris, J. K.

    مصطلحات موضوعية: Child, Cohort Studie, Europe, Female, Human, Infant, Newborn, Pregnancy, Registries

    وصف الملف: STAMPA

    Relation: info:eu-repo/semantics/altIdentifier/pmid/35351164; info:eu-repo/semantics/altIdentifier/wos/WOS:000775075600002; volume:17; issue:1; firstpage:142-1; lastpage:142-11; numberofpages:11; journal:ORPHANET JOURNAL OF RARE DISEASES; https://hdl.handle.net/11392/2489298; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85127261034; https://ojrd.biomedcentral.com/articles/10.1186/s13023-022-02292-y