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von Loviglio, M. N ; Leleu, M. ; Männik, K. ; et al.
Schlagworte: Molecular Biology; Cellular and Molecular Neuroscience; Psychiatry and Mental Health
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von Maillard AM ; Ruef A ; Pizzagalli F ; et al.
Schlagworte: Adolescent; Adult; Anthropometry; Arabidopsis Protein; Autistic Disorder; Body Mass Index; Brain; Brain Mapping; Child; Chromosomes; Human; Pair 16; DNA Copy Number Variation; Female; Gene Dosage; Genetic Association Studie; Intramolecular Transferase; Male; Middle Aged; Obesity; Phenotype; Psychiatric Status Rating Scale; Schizophrenia; Young Adult
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von Boyle, B ; Morris, JK ; McConkey, R ; et al.
BJOG An International Journal of Obstetrics & Gynaecology, vol 121, iss 7
Schlagworte: 3215 Reproductive Medicine (for-2020); 32 Biomedical and Clinical Sciences (for-2020); Pediatric (rcdc); Pregnancy (rcdc); Brain Disorders (rcdc); Genetics (rcdc); Genetic Testing (rcdc); Intellectual and Developmental Disabilities (IDD) (rcdc); Down Syndrome (rcdc); Perinatal Period - Conditions Originating in Perinatal Period (rcdc); Women's Health (rcdc); Congenital (hrcs-hc); Reproductive health and childbirth (hrcs-hc); 3 Good Health and Well Being (sdg); Adult (mesh); Down Syndrome (mesh); Europe (mesh); Female (mesh); Humans (mesh); Maternal Age (mesh); Middle Aged (mesh); Pregnancy (mesh); Pregnancy Outcome (mesh); Pregnancy; Multiple (mesh); Prenatal Diagnosis (mesh); Prevalence (mesh); Risk (mesh); Risk Assessment (mesh); Twins
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von Jaureguiberry, G ; De la Dure-Molla, M ; Parry, D ; et al.
Nephron Physiology , 122 (1-2) 1 - 6. (2012)
Schlagworte: Adolescent; Adult; Amelogenesis imperfecta; Child; Consanguinity; Dental enamel proteins; Exome; Family health; Female; Genes; Recessive; Genetic predisposition to disease; Genome-wide association study; Humans; Male; Middle aged; Mutation; Nephrocalcinosis; Pedigree; Sequence Analysis; DNA; Syndrome; Young Adult
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von Hwang, CS ; Sukalo, M ; Batygin, O ; et al.
Schlagworte: TERMINAL ACETYLTRANSFERASE; DEGRADATION SIGNALS; CARDIOVASCULAR DEVELOPMENT; RECOGNITION COMPONENT; CYTOSOLIC PROTEINS; PROTEASOME SYSTEM; STRUCTURAL BASIS; MICE LACKING; DNA-REPAIR; E3
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Schlagworte: Epidemiology
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von Morris, J.K. ; Garne, E. ; Loane, M. ; et al.
European journal of medical genetics 61 (2018): 479–482. doi:10.1016/j.ejmg.2018.05.008 ; info:cnr-pdr/source/autori:Morris, J.K.; Garne, E.; Loane, M.; Addor, MC; 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, H. E.K.; Zymak-Zakutnia, N.; Rankin, J./titolo:Prevalence of valproate syndrome in Europe from 2005 to 2014: A registry based multi-centre study/doi:10.1016j.ejmg.2018.05.008/rivista:European journal of medical genetics/anno:2018/pagina_da:479/pagina_a:482/intervallo_pagine:479–482/volume:61
Schlagworte: Congenital anomaly; Sodium valproate; Valproic acid
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von Boyle B 1 ; 2 ; Addor MC 3 ; et al.
Archives of disease in childhood. Fetal and neonatal edition 2017 (2017): F1–F8. doi:10.1136/archdischild-2016-311845 ; info:cnr-pdr/source/autori:Boyle B 1,2, Addor MC 3, Arriola L 4, Barisic I5, Bianchi F 6, Csáky-Szunyogh M 7, de Walle HEK 8, Dias CM 9, Draper E 10, Gatt M 11, Garne E 12, Haeusler M 13, Källén K 14, Latos-Bielenska A 15, McDonnell B 16, Mullaney C 17, Nelen V 18, Neville AJ 19, O'Mahony M 20, Queisser-Wahrendorf A 21, Randrianaivo H 22, Rankin J 23, Rissmann A 24, Ritvanen A 25, Rounding C 26, Tucker D 27, Verellen-Dumoulin C 28, Wellesley D 29, Wreyford ....
Schlagworte: Congenital anomaly; DALY; Global Burden of Disease; YLL; mortality
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von Faber, HH ; Bouman, K ; Walle, HEK ; et al.
Serveur académique Lausannois ; Prenatal Diagnosis / 19th International Conference on Prenatal Diagnosis, Washington July 2015, vol. 35
Schlagworte: demo; geo
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von Hauschild, M ; Martinet, D ; Phan Hug, F ; et al.
Serveur académique Lausannois ; Congrès de la Société Suisse d'endocrinologie pédiatrique, Septembre 2013
Schlagworte: hist; lang
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von Greenlees, R (Greenlees, Ruth) 1 ; Neville, A (Neville, Amanda) 2 ; Addor, MC (Addor, Marie-Claude) 3 ; et al.
Birth defects research. Part A. Clinical and molecular teratology (Online) 91 (2011): S51–S100. doi:10.1002/bdra.20775 ; info:cnr-pdr/source/autori:Greenlees, R (Greenlees, Ruth)[ 1 ] ; Neville, A (Neville, Amanda)[ 2 ] ; Addor, MC (Addor, Marie-Claude)[ 3 ] ; Amar, E (Amar, Emmanuelle)[ 4 ] ; Arriola, L (Arriola, Larraitz)[ 5 ] ; Bakker, M (Bakker, Marian)[ 6 ] ; Barisic, I (Barisic, Ingeborg)[ 7 ] ; Boyd, PA (Boyd, Patricia A.)[ 8 ] ; Calzolari, E (Calzolari, Elisa)[ 2 ] ; Doray, B (Doray, Berenice)[ 9 ] ; Draper, E (Draper, Elizabeth)[ 10 ] ; Vollset, SE (Vollset, Stein Emil)[ 11 ....
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von BUSBY A ; ARMSTRONG BM ; DOLK H ; et al.
Schlagworte: NTDs
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von Luteijn JM ; Addor MC ; Arriola L ; et al.
Epidemiology (Online) 26 (2015): 853–861. doi:10.1097/EDE.0000000000000372. ; info:cnr-pdr/source/autori:Luteijn JM, Addor MC, Arriola L, Bianchi F, Garne E, Khoshnood B, Nelen V, Neville A, Queisser-Luft A, Rankin J, Rounding C, Verellen-Dumoulin C, de Walle H, Wellesley D, Wreyford B, Yevtushok L, de Jong-van den Berg L, Morris J, Dolk H./titolo:The Association of H1N1 Pandemic Influenza with Congenital Anomaly Prevalence in Europe: An Ecological Time Series Study/doi:10.1097EDE.0000000000000372./rivista:Epidemiology (Online)/anno:2015/pagina_da:853/pagina_a:861/intervallo_pagine:853–861/volume:26
Schlagworte: The Association of H1N1 Pandemic Influenza; Congenital Anomaly
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