المؤلفون: Morris, JK, Bergman, JEH, Barisic, I, Wellesley, D, Tucker, D, Limb, E, Addor, M-C, Cavero-Carbonell, C, Matias Dias, C, Draper, ES, Echevarría-González-de-Garibay, LJ, Gatt, M, Klungsøyr, K, Lelong, N, Luyt, K, Materna-Kiryluk, A, Nelen, V, Neville, A, Perthus, I, Pierini, A, Randrianaivo-Ranjatoelina, H, Rankin, J, Rissmann, A, Rouget, F, Sayers, G, Wertelecki, W, Kinsner-Ovaskainen, A, Garne, E

وصف الملف: application/pdf; application/vnd.openxmlformats-officedocument.wordprocessingml.document

العلاقة: https://openaccess.sgul.ac.uk/id/eprint/115921/1/s41431-023-01502-w.pdfTest; https://openaccess.sgul.ac.uk/id/eprint/115921/6/41431_2023_1502_MOESM1_ESM.docxTest; Morris, JK; Bergman, JEH; Barisic, I; Wellesley, D; Tucker, D; Limb, E; Addor, M-C; Cavero-Carbonell, C; Matias Dias, C; Draper, ES; et al. Morris, JK; Bergman, JEH; Barisic, I; Wellesley, D; Tucker, D; Limb, E; Addor, M-C; Cavero-Carbonell, C; Matias Dias, C; Draper, ES; Echevarría-González-de-Garibay, LJ; Gatt, M; Klungsøyr, K; Lelong, N; Luyt, K; Materna-Kiryluk, A; Nelen, V; Neville, A; Perthus, I; Pierini, A; Randrianaivo-Ranjatoelina, H; Rankin, J; Rissmann, A; Rouget, F; Sayers, G; Wertelecki, W; Kinsner-Ovaskainen, A; Garne, E (2024) Surveillance of multiple congenital anomalies; searching for new associations. Eur J Hum Genet, 32 (4). pp. 407-412. ISSN 1476-5438 https://doi.org/10.1038/s41431-023-01502-wTest SGUL Authors: Morris, Joan Katherine

الإتاحة: https://doi.org/10.1038/s41431-023-01502-wTest
https://openaccess.sgul.ac.uk/id/eprint/115921Test/
https://openaccess.sgul.ac.uk/id/eprint/115921/1/s41431-023-01502-w.pdfTest
https://openaccess.sgul.ac.uk/id/eprint/115921/6/41431_2023_1502_MOESM1_ESM.docxTest

المؤلفون: Morris, JK, Garne, E, Loane, M, Addor, M-C, Barisic, I, Bianchi, F, Gatt, M, Lanzoni, M, Lynch, C, Mokoroa, O, Nelen, V, Neville, A, O'Mahony, MT, Randrianaivo-Ranjatoelina, H, Rissmann, A, Tucker, D, de Walle, HEK, Zymak-Zakutnia, N, Rankin, J

مصطلحات موضوعية: Congenital anomaly, Sodium valproate, Valproic acid, Adult, Anticonvulsants, Cognitive Dysfunction, Congenital Abnormalities, Epilepsy, Europe, Female, Humans, Pregnancy, Pregnancy Complications, Registries, Syndrome

وصف الملف: 479 - 482

العلاقة: Eur J Med Genet; http://qmro.qmul.ac.uk/xmlui/handle/123456789/42427Test

الإتاحة: https://doi.org/10.1016/j.ejmg.2018.05.008Test
http://qmro.qmul.ac.uk/xmlui/handle/123456789/42427Test

المؤلفون: Morris, J.K., Garne, E., Loane, M., Addor, M.C., Barisic, I., Bianchi, F., Gatt, M., Lanzoni, M., Lynch, C., Mokoroa, O., Nelen, V., Neville, A., O'Mahony, M.T., Randrianaivo-Ranjatoelina, H., Rissmann, A., Tucker, D., de Walle, HEK, Zymak-Zakutnia, N., Rankin, J.

المصدر: European journal of medical genetics, vol. 61, no. 9, pp. 479-482

مصطلحات موضوعية: Adult, Anticonvulsants/adverse effects, Cognitive Dysfunction/epidemiology, Cognitive Dysfunction/etiology, Congenital Abnormalities/epidemiology, Congenital Abnormalities/etiology, Epilepsy/drug therapy, Europe, Female, Humans, Pregnancy, Pregnancy Complications/drug therapy, Registries, Syndrome, Valproic Acid/adverse effects, Congenital anomaly, Sodium valproate, Valproic acid

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/29753923; info:eu-repo/semantics/altIdentifier/eissn/1878-0849; https://serval.unil.ch/notice/serval:BIB_DCD99F62608ATest; urn:issn:1769-7212

الإتاحة: https://doi.org/10.1016/j.ejmg.2018.05.008Test
https://serval.unil.ch/notice/serval:BIB_DCD99F62608ATest

المؤلفون: Garne, E., Loane, M., Dolk, H., Barisic, I., Addor, M.C., Arriola, L., Bakker, M., Calzolari, E., Matias Dias, C., Doray, B., Gatt, M., Melve, K.K., Nelen, V., O'Mahony, M., Pierini, A., Randrianaivo-Ranjatoelina, H., Rankin, J., Rissmann, A., Tucker, D., Verellun-Dumoulin, C., Wiesel, A.

المصدر: Birth Defects Research. Part A, Clinical and Molecular Teratology, vol. 94, no. 3, pp. 134-140

مصطلحات موضوعية: Adult, Congenital Abnormalities/epidemiology, Congenital Abnormalities/etiology, Diabetes Mellitus, Ear/abnormalities, Europe/epidemiology, Female, Heart Defects, Congenital/epidemiology, Congenital/etiology, Hernia, Umbilical/epidemiology, Umbilical/etiology, Humans, Infant, Newborn, Live Birth, Male, Neural Tube Defects/epidemiology, Neural Tube Defects/etiology, Population Surveillance/methods, Pregnancy, Pregnancy Complications/epidemiology, Pregnancy in Diabetics/epidemiology, Registries, Risk Factors, Young Adult

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/22371321; info:eu-repo/semantics/altIdentifier/eissn/1542-0760; https://serval.unil.ch/notice/serval:BIB_A0BD24C0B9F7Test; urn:issn:1542-0752

الإتاحة: https://doi.org/10.1002/bdra.22886Test
https://serval.unil.ch/notice/serval:BIB_A0BD24C0B9F7Test

المؤلفون: Garne, E., Loane, M., Dolk, H., Barisic, I., Addor, M.C., Arriola, L., Bakker, M., Calzolari, E., Matias Dias, C., Doray, B., Gatt, M., Melve, K.K., Nelen, V., O'Mahony, M., Pierini, A., Randrianaivo-Ranjatoelina, H., Rankin, J., Rissmann, A., Tucker, D., Verellun-Dumoulin, C., Wiesel, A.

المصدر: Serveur académique Lausannois ; Birth Defects Research. Part A, Clinical and Molecular Teratology, vol. 94, no. 3, pp. 134-140

مصطلحات موضوعية: demo, envir

العلاقة: urn:issn:1542-0752; 10670/1.egrked; https://serval.unil.ch/notice/serval:BIB_A0BD24C0B9F7Test

الإتاحة: https://doi.org/10.1002/bdra.22886Test
https://serval.unil.ch/notice/serval:BIB_A0BD24C0B9F7Test

المؤلفون: Greenlees, R, Neville, A, Calzolari, E, Addor, M-C, Amar, E, Arriola, L, Bakker, M, Barisic, I, Boyd, PA, Doray, B, Draper, E, Emil Vollset S, Garne, E, Gatt, M, Haeusler, M, Kallen, K, Khoshnood, B, Latos-Bielenska, A, Materna-Kiryluk, A, Martinez-Frias, M-L, Matias Dias C, Mcdonnell, B, Mullaney, C, Nelen, V, O'Mahony, M, Pierini, A, Queisser-Luft, A, Randrianaivo-Ranjatoélina, H, Rankin, J, Rissmann, A, Ritvanen, A, Salvador, J, Sipek, A, Tucker, D, Verellen-Dumoulin, C, Wellesley, D, Wertelecki, W

المصدر: Scopus ; http://www.scopus.com/home.urlTest

وصف الملف: metadata

العلاقة: BIRTH DEFECTS RESEARCH PART A - CLINICAL AND MOLECULAR TERATOLOGY, 2011, 91 (SUPPL. 1); http://hdl.handle.net/2381/26720Test

الإتاحة: https://doi.org/10.1002/bdra.20775Test
http://hdl.handle.net/2381/26720Test

المؤلفون: Greenlees R, Neville A, Addor MC, Amar E, Arriola L, Bakker M, Barisic I, Boyd PA, Calzolari E, Doray B, Draper E, Vollset SE, Garne E, Gatt M, Haeusler M, Kallen K, Khoshnood B, Latos-Bielenska A, Martinez-Frias ML, Materna-Kiryluk A, Dias CM, McDonnell B, Mullaney C, Nelen V, OMahony M, Pierini A, Queisser-Luft A, Randrianaivo-Ranjatoélina H, Rankin J, Rissmann A, Ritvanen A, Salvador J, Sipek A, Tucker D, Verellen-Dumoulin C, Wellesley D, Wertelecki W

المساهمون: TITO

مصطلحات موضوعية: HYTE

وصف الملف: S51 - S100

العلاقة: Birth Defects Research. Part A; 91; http://www.julkari.fi/handle/10024/106193Test

الإتاحة: http://www.julkari.fi/handle/10024/106193Test

المؤلفون: Greenlees R, Neville A, Addor MC, Amar E, Arriola L, Bakker M, Barisic I, Boyd PA, Calzolari E, Doray B, Draper E, Vollset SE, Garne E, Gatt M, Haeusler M, Kallen K, Khoshnood B, Latos-Bielenska A, Martinez-Frias ML, Materna-Kiryluk A, Dias CM, McDonnell B, Mullaney C, Nelen V, OMahony M, Pierini A, Queisser-Luft A, Randrianaivo-Ranjatoélina H, Rankin J, Rissmann A, Ritvanen A, Salvador J, Sipek A, Tucker D, Verellen-Dumoulin C, Wellesley D, Wertelecki W

المساهمون: TITO

مصطلحات موضوعية: HYTE

وصف الملف: S51 - S100

العلاقة: Birth Defects Research. Part A; 91; http://www.julkari.fi/handle/10024/81527Test

الإتاحة: http://www.julkari.fi/handle/10024/81527Test

المؤلفون: Greenlees, R., Neville, A., Addor, M.C., Amar, E., Arriola, L., Bakker, M., Barisic, I., Boyd, P.A., Calzolari, E., Doray, B., Draper, E., Vollset, S.E., Garne, E., Gatt, M., Haeusler, M., Kallen, K., Khoshnood, B., Latos-Bielenska, A., Martinez-Frias, M.L., Materna-Kiryluk, A., Dias, C.M., McDonnell, B., Mullaney, C., Nelen, V., O'Mahony, M., Pierini, A., Queisser-Luft, A., Randrianaivo-Ranjatoélina, H., Rankin, J., Rissmann, A., Ritvanen, A., Salvador, J., Sipek, A., Tucker, D., Verellen-Dumoulin, C., Wellesley, D., Wertelecki, W.

المصدر: Birth Defects Research. Part A, Clinical and Molecular Teratology, vol. 91, no. Suppl. 1, pp. S51-S100

مصطلحات موضوعية: Abortion, Induced/statistics & numerical data, Committee Membership, Congenital Abnormalities/epidemiology, Databases, Factual, Europe%2Fepidemiology%22">Type="Geographic">Europe/epidemiology, Evaluation Studies as Topic, Female, Fetal Death/epidemiology, Humans, Internet, Population Surveillance, Pregnancy, Prenatal Diagnosis, Prevalence, Registries/statistics & numerical data, Stillbirth/epidemiology

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/21381185; info:eu-repo/semantics/altIdentifier/eissn/1542-0760; https://serval.unil.ch/notice/serval:BIB_4FA4255CB1F0Test; urn:issn:1542-0752

الإتاحة: https://doi.org/10.1002/bdra.20775Test
https://serval.unil.ch/notice/serval:BIB_4FA4255CB1F0Test

المؤلفون: Morris, J.K., Bergman, JEH, Barisic, I., Wellesley, D., Tucker, D., Limb, E., Addor, M.C., Cavero-Carbonell, C., Matias Dias, C., Draper, E.S., Echevarría-González-de-Garibay, L.J., Gatt, M., Klungsøyr, K., Lelong, N., Luyt, K., Materna-Kiryluk, A., Nelen, V., Neville, A., Perthus, I., Pierini, A., Randrianaivo-Ranjatoelina, H., Rankin, J., Rissmann, A., Rouget, F., Sayers, G., Wertelecki, W., Kinsner-Ovaskainen, A., Garne, E.

المصدر: European journal of human genetics

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/38052905; info:eu-repo/semantics/altIdentifier/eissn/1476-5438; https://serval.unil.ch/notice/serval:BIB_D5E08218E6E9Test; urn:issn:1018-4813

الإتاحة: https://doi.org/10.1038/s41431-023-01502-wTest
https://serval.unil.ch/notice/serval:BIB_D5E08218E6E9Test