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1. Predicting Matching Quality of Record Linkage Algorithms on Growing Data Sets
by Schuster, Martin and Tittmann, Lukas and Wolf, Andreas
Studies in health technology and informatics, ISSN 0926-9630, 2018, Volume 253, pp. 70 - 74
parameterization | data integration | Record linkage | Algorithms | Medical Record Linkage | Data Accuracy | Information Storage and Retrieval
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2. Full Text Rare Variants in Specific Lysosomal Genes Are Associated With Parkinson's Disease
by Hopfner, Franziska and Mueller, Stefanie H and Szymczak, Silke and Junge, Olaf and Tittmann, Lukas and May, Sandra and Lohmann, Katja and Grallert, Harald and Lieb, Wolfgang and Strauch, Konstantin and Müller‐Nurasyid, Martina and Berger, Klaus and Schormair, Barbara and Winkelmann, Juliane and Mollenhauer, Brit and Trenkwalder, Claudia and Maetzler, Walter and Berg, Daniela and Kasten, Meike and Klein, Christine and Höglinger, Günter U and Gasser, Thomas and Deuschl, Günther and Franke, André and Krawczak, Michael and Dempfle, Astrid and Kuhlenbäumer, Gregor
Movement disorders, ISSN 0885-3185, 07/2020, Volume 35, Issue 7, pp. 1245 - 1248
Parkinson's disease | LAMP1 | VPS13C | GBA | ATP13A2 | α‐synuclein | Lysosme | TMEM175 | chaperone‐mediated‐autophagy | Clinical Neurology | Neurosciences & Neurology | Life Sciences & Biomedicine | Science & Technology | Genetic variance | Neurodegenerative diseases | Parkinsons disease | Lysosomes | Glucosylceramidase | Genomes | Synuclein | Movement disorders | DNA sequencing | Index Medicus
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3. Full Text Reduced microbiome alpha diversity in young patients with ADHD
by Prehn-Kristensen, Alexander and Zimmermann, Alexandra and Tittmann, Lukas and Lieb, Wolfgang and Schreiber, Stefan and Baving, Lioba and Fischer, Annegret
PloS one, ISSN 1932-6203, 07/2018, Volume 13, Issue 7, pp. e0200728 - e0200728
Science & Technology - Other Topics | Multidisciplinary Sciences | Science & Technology | Neisseria - isolation & purification | Attention Deficit Disorder with Hyperactivity - microbiology | Humans | Gastrointestinal Microbiome | Male | Biodiversity | Neisseria - classification | DNA, Bacterial - genetics | Attention Deficit Disorder with Hyperactivity - genetics | Adolescent | RNA, Bacterial - genetics | RNA, Ribosomal, 16S - genetics | Child | Neisseria - genetics | DNA, Ribosomal - genetics | Care and treatment | Research | Microbiota (Symbiotic organisms) | Analysis | Attention-deficit hyperactivity disorder | Biological diversity | rRNA 16S | Mental disorders | Hyperactivity | Pathogenesis | Microbiomes | Families & family life | Psychotherapy | Alcohol | Systematic review | Mental depression | Microbiota | Microorganisms | Teenagers | Intestinal microflora | Immune system | Dopamine | Attention deficit hyperactivity disorder | Behavior disorders | Patients | Children & youth | Studies | Autism | Hospitals | Biomarkers | Cocaine | Impulsive behavior | Molecular biology | Child & adolescent psychiatry | Index Medicus
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4. Full Text The impact of rare variants in FUS in essential tremor
by Hopfner, Franziska and Stevanin, Giovanni and Müller, Stefanie H and Mundwiller, Emeline and Bungeroth, May and Durr, Alexandra and Pendziwiat, Manuela and Anheim, Mathieu and Schneider, Susanne A and Tittmann, Lukas and Klebe, Stephan and Lorenz, Delia and Deuschl, Günther and Brice, Alexis and Kuhlenbäumer, Gregor
Movement disorders, ISSN 0885-3185, 04/2015, Volume 30, Issue 5, pp. 721 - 724
tremor | essential tremor | genetics | meta‐analysis | FUS | Genetics | Tremor | Essential tremor | Meta-analysis | Clinical Neurology | Neurosciences & Neurology | Life Sciences & Biomedicine | Science & Technology | Essential Tremor - genetics | Humans | Middle Aged | RNA-Binding Protein FUS - genetics | Male | Mutation - genetics | Databases, Bibliographic - statistics & numerical data | DNA Mutational Analysis | Aged, 80 and over | Adult | Female | Aged | France | Germany | Index Medicus
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5. Phenotypes of organ involvement in sarcoidosis
by Schupp, Jonas Christian and Freitag-Wolf, Sandra and Bargagli, Elena and Mihailović-Vučinić, Violeta and Rottoli, Paola and Grubanovic, Aleksandar and Müller, Annegret and Jochens, Arne and Tittmann, Lukas and Schnerch, Jasmin and Olivieri, Carmela and Fischer, Annegret and Jovanovic, Dragana and Filipovic, Snežana and Videnovic-Ivanovic, Jelica and Bresser, Paul and Jonkers, René and O’Reilly, Kate and Ho, Ling-Pei and Gaede, Karoline I and Zabel, Peter and Dubaniewicz, Anna and Marshall, Ben and Kieszko, Robert and Milanowski, Janusz and Günther, Andreas and Weihrich, Anette and Petrek, Martin and Kolek, Vitezslav and Keane, Michael P and O’Beirne, Sarah and Donnelly, Seamas and Haraldsdottir, Sigridur Olina and Jorundsdottir, Kristin B and Costabel, Ulrich and Bonella, Francesco and Wallaert, Benoît and Grah, Christian and Peroš-Golubičić, Tatjana and Luisetti, Mauritio and Kadija, Zamir and Pabst, Stefan and Grohé, Christian and Strausz, János and Vašáková, Martina and Sterclova, Martina and Millar, Ann and Homolka, Jiří and Slováková, Alena and Kendrick, Yvonne and Crawshaw, Anjali and Wuyts, Wim and Spencer, Lisa and Pfeifer, Michael and Valeyre, Dominique and Poletti, Venerino and Wirtz, Hubertus and Prasse, Antje and Schreiber, Stefan and Krawczak, Michael and Müller-Quernheim, Joachim
The European respiratory journal, ISSN 0903-1936, 01/2018, Volume 51, Issue 1, pp. 1700991 - 1700991
Life Sciences & Biomedicine | Respiratory System | Science & Technology | Sarcoidosis - diagnosis | Acute Disease | Europe | Humans | Middle Aged | European Continental Ancestry Group | Genotype | Male | Lung - physiopathology | Tertiary Healthcare | Lymph Nodes - physiopathology | Abdomen | Forced Expiratory Volume | Phenotype | Sarcoidosis - physiopathology | Skin Diseases - physiopathology | Adult | Female | Aged | Lung Diseases - physiopathology | Skin - physiopathology | Eye Diseases - physiopathology | Eye - physiopathology | Joint Diseases - physiopathology | Phenotypes | Sarcoidosis | Central nervous system | Fatigue | Skin | Heart diseases | Genotypes | Lymph nodes
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6. Full Text Genome-wide association study in essential tremor identifies three new loci
by Müller, Stefanie H and Girard, Simon L and Hopfner, Franziska and Merner, Nancy D and Bourassa, Cynthia V and Lorenz, Delia and Clark, Lorraine N and Tittmann, Lukas and Soto-Ortolaza, Alexandra I and Klebe, Stephan and Hallett, Mark and Schneider, Susanne A and Hodgkinson, Colin A and Lieb, Wolfgang and Wszolek, Zbigniew K and Pendziwiat, Manuela and Lorenzo-Betancor, Oswaldo and Poewe, Werner and Ortega-Cubero, Sara and Seppi, Klaus and Rajput, Alex and Hussl, Anna and Rajput, Ali H and Berg, Daniela and Dion, Patrick A and Wurster, Isabel and Shulman, Joshua M and Srulijes, Karin and Haubenberger, Dietrich and Pastor, Pau and Vilariño-Güell, Carles and Postuma, Ronald B and Bernard, Geneviève and Ladwig, Karl-Heinz and Dupré, Nicolas and Jankovic, Joseph and Strauch, Konstantin and Panisset, Michel and Winkelmann, Juliane and Testa, Claudia M and Reischl, Eva and Zeuner, Kirsten E and Ross, Owen A and Arzberger, Thomas and Chouinard, Sylvain and Deuschl, Günther and Louis, Elan D and Kuhlenbäumer, Gregor and Rouleau, Guy A
Brain (London, England : 1878), ISSN 0006-8950, 2016, Volume 139, Issue 12, pp. 3163 - 3169
Genetics | Genome-wide association study | Tremor | Essential tremor | Movement disorders | Neurosciences | Clinical Neurology | Neurosciences & Neurology | Life Sciences & Biomedicine | Science & Technology | Peroxisome Proliferator-Activated Receptor Gamma Coactivator 1-alpha - genetics | Genome-Wide Association Study | Essential Tremor - genetics | Humans | Protein-Serine-Threonine Kinases - genetics | Polymorphism, Single Nucleotide | alpha Catenin - genetics | Index Medicus | Abridged Index Medicus | tremor | genetics | genome-wide association study | essential tremor | 1030 | movement disorders | Original
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7. Full Text No association between Parkinson disease and autoantibodies against NMDA-type glutamate receptors
by Hopfner, Franziska and Mueller, Stefanie H and Steppat, Dagmar and Miller, Joanna and Schmidt, Nele and Wandinger, Klaus-Peter and Leypoldt, Frank and Berg, Daniela and Franke, Andre and Lieb, Wolfgang and Tittmann, Lukas and Balzer-Geldsetzer, Monika and Baudrexel, Simon and Dodel, Richard and Hilker-Roggendorf, Ruediger and Kalbe, Elke and Kassubek, Jan and Klockgether, Thomas and Liepelt-Scarfone, Inga and Mollenhauer, Brit and Neuser, Petra and Reetz, Kathrin and Riedel, Oliver and Schulte, Claudia and Schulz, Joerg B and Spottke, Annika and Storch, Alexander and Trenkwalder, Claudia and Wittchen, Hans-Ulrich and Witt, Karsten and Wuellner, Ullrich and Deuschl, Gunther and Kuhlenbaeumer, Gregor
Translational neurodegeneration, ISSN 2047-9158, 04/2019, Volume 8, Issue 1, pp. 11 - 11
Neurosciences | Neurosciences & Neurology | Life Sciences & Biomedicine | Science & Technology | Studies | Encephalitis | Medical research | Neurology | Emotional disorders | Memory | Parkinsons disease | Cognitive ability | Standard deviation | Patients | Age | Dementia | Parkinson disease | NMDA IgA/IgM antibodies | NMDA antibody | Cognitive impairment
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8. Full Text Private variants in PRKN are associated with late-onset Parkinson's disease
by Hopfner, Franziska and Mueller, Stefanie H and Szymczak, Silke and Junge, Olaf and Tittmann, Lukas and May, Sandra and Lohmann, Katja and Grallert, Harald and Lieb, Wolfgang and Strauch, Konstantin and Müller-Nurasyid, Martina and Berger, Klaus and Schormair, Barbara and Winkelmann, Juliane and Mollenhauer, Brit and Trenkwalder, Claudia and Maetzler, Walter and Berg, Daniela and Kasten, Meike and Klein, Christine and Höglinger, Günter U and Gasser, Thomas and Deuschl, Günther and Franke, André and Krawczak, Michael and Dempfle, Astrid and Kuhlenbäumer, Gregor
Parkinsonism & related disorders, ISSN 1353-8020, 06/2020, Volume 75, pp. 24 - 26
PRKN | Genetics | PINK1 | Parkinson's disease | PARK7 | Clinical Neurology | Neurosciences & Neurology | Life Sciences & Biomedicine | Science & Technology | Index Medicus
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9. Full Text Rare variants in ANO3 are not a susceptibility factor in essential tremor
by Hopfner, Franziska and Bungeroth, May and Pendziwiat, Manuela and Tittmann, Lukas and Deuschl, Günther and Schneider, Susanne A and Kuhlenbäumer, Gregor
Parkinsonism & related disorders, ISSN 1353-8020, 2013, Volume 20, Issue 1, pp. 134 - 135
Neurology | Genetics | Dystonia | Tremor | Essential tremor | ANO3 | Clinical Neurology | Neurosciences & Neurology | Life Sciences & Biomedicine | Science & Technology | Genetic Predisposition to Disease - genetics | Essential Tremor - genetics | Humans | Middle Aged | Female | Male | Aged | Polymorphism, Single Nucleotide | Anoctamins | Chloride Channels - genetics | Reverse Transcriptase Polymerase Chain Reaction | Index Medicus
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10. Full Text The impact of rare variants in FUS in essential tremor
: FUS in ET
by Hopfner, Franziska and Stevanin, Giovanni and Müller, Stefanie H and Mundwiller, Emeline and Bungeroth, May and Durr, Alexandra and Pendziwiat, Manuela and Anheim, Mathieu and Schneider, Susanne A and Tittmann, Lukas and Klebe, Stephan and Lorenz, Delia and Deuschl, Günther and Brice, Alexis and Kuhlenbäumer, Gregor
Movement disorders, ISSN 0885-3185, 04/2015, Volume 30, Issue 5, pp. 721 - 724
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11. Full Text Genome-wide association study of myocardial infarction, atrial fibrillation, acute stroke, acute kidney injury and delirium after cardiac surgery - a sub-analysis of the RIPHeart-Study
by Westphal, Sabine and Stoppe, Christian and Stoppe, Christian and Gruenewald, Matthias and Gruenewald, Matthias and Bein, Berthold and Renner, Jochen and Renner, Jochen and Cremer, Jochen and Cremer, Jochen and Coburn, Mark and Coburn, Mark and Schaelte, Gereon and Schaelte, Gereon and Boening, Andreas and Niemann, Bernd and Niemann, Bernd and Kletzin, Frank and Kletzin, Frank and Roesner, Jan and Roesner, Jan and Strouhal, Ulrich and Strouhal, Ulrich and Reyher, Christian and Laufenberg-Feldmann, Rita and Ferner, Marion and Ferner, Marion and Brandes, Ivo F and Bauer, Martin and Kortgen, Andreas and Kortgen, Andreas and Stehr, Sebastian N and Stehr, Sebastian N and Wittmann, Maria and Wittmann, Maria and Baumgarten, Georg and Struck, Rafael and Meyer-Treschan, Tanja and Meyer-Treschan, Tanja and Kienbaum, Peter and Kienbaum, Peter and Heringlake, Matthias and Schoen, Julika and Schoen, Julika and Sander, Michael and Sander, Michael and Treskatsch, Sascha and Treskatsch, Sascha and Smul, Thorsten and Wolwender, Ewa and Wolwender, Ewa and Schilling, Thomas and Degenhardt, Frauke and Degenhardt, Frauke and Franke, Andre and Mucha, Soeren and Tittmann, Lukas and Tittmann, Lukas and Kohlhaas, Madeline and Fuernau, Georg and Brosteanu, Oana and Brosteanu, Oana and Hasenclever, Dirk and Hasenclever, Dirk and Zacharowski, Kai and Meybohm, Patrick and Stevanovic, Ana and Rossaint, Rolf and Felzen, Marc and Goetzenich, Andreas and Moormann, Tobias and Chalk, Katharina and Knuefermann, Pascal and Boehm, Olaf and Hoeft, Andreas and Iken, Sonja and Weber, Christian and Wiedenbeck, Carolin and Schwarzmann, Gerhard and Pense, Karin and Goerlach, Gerold and Wollbrueck, Matthias and Weigand, Markus and Strauchmann, Julia and August, Konrad and Morsbach, Kai U and Paxian, Markus and Reinhard, Konrad and Scholz, Jens and Broch, Ole and Albrecht, Martin and Heinze, Hermann and Paarmann, Hauke and Sievers, Hans-Hinrich and Hachenberg, Thomas and Werner, Christian and Mauff, Susanne and Alms, Angela and Bergt, Stefan and Roewer, Norbert and RIPHeart-Study Collaborators
BMC cardiovascular disorders, ISSN 1471-2261, 01/2019, Volume 19, Issue 1, pp. 26 - 26
Delirium | Myocardial infarction | Stroke | Genome-wide association study | Acute kidney injury | Atrial fibrillation | Cardiac surgery | Cardiac & Cardiovascular Systems | Life Sciences & Biomedicine | Cardiovascular System & Cardiology | Science & Technology | Myocardial Infarction - genetics | Cytoskeletal Proteins - genetics | Humans | Middle Aged | Stroke - diagnosis | Male | Acute Kidney Injury - genetics | Cardiac Surgical Procedures - adverse effects | Stroke - genetics | Multicenter Studies as Topic | Delirium - genetics | Dual-Specificity Phosphatases - genetics | Female | Atrial Fibrillation - diagnosis | Myocardial Infarction - diagnosis | HSC70 Heat-Shock Proteins - genetics | Genetic Predisposition to Disease | Genome-Wide Association Study | Risk Factors | Treatment Outcome | Atrial Fibrillation - genetics | Mitogen-Activated Protein Kinase Phosphatases - genetics | Randomized Controlled Trials as Topic | Phosphoprotein Phosphatases - genetics | Ryanodine Receptor Calcium Release Channel - genetics | Acute Kidney Injury - diagnosis | Aged | Polymorphism, Single Nucleotide | Delirium - diagnosis | Heart | Medical research | Genome-wide association studies | Usage | Complications | Surgery | Medicine, Experimental | Genetic aspects | Research | Heart attack | Risk factors | Oxidative stress | Cardiac arrhythmia | Heart attacks | Heart surgery | Clinical trials | Ryanodine receptors | Cardiovascular disease | Genomes | Single-nucleotide polymorphism | Fibrillation | Ischemia | Rodents | Chromosomes | Cerebral infarction | Kidneys | Mortality | Studies | Genetic variance | Coronary vessels | Quality control | Renal failure | Index Medicus
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12. Full Text Genome-wide association analyses identify new risk variants and the genetic architecture of amyotrophic lateral sclerosis
by Shatunov, Aleksey and Dekker, Annelot M and Diekstra, Frank P and Pulit, Sara L and de Jong, Simone and Robinson, Matthew R and Yang, Jian and van Doormaal, Perry T. C and Blokhuis, Anna M and Sproviero, William and Jones, Ashley R and Kenna, Kevin P and van Eijk, Kristel R and Harschnitz, Oliver and Vajda, Alice and Ticozzi, Nicola and Rogelj, Boris and Ravnik-Glavac, Metka and Koritnik, Blazi and Zidar, Janez and Leonardis, Lea and Groselj, Leja Dolenc and Millecamps, Stephanie and Meininger, Vincent and de Carvalho, Mamede and Mora, Jesus S and Rojas-Garcia, Ricardo and Colville, Shuna and Swingler, Robert and Shaw, Pamela J and Hardy, John and Pittman, Alan and Sidle, Katie and Topp, Simon and Petri, Susanne and Drepper, Carsten and Meyer, Thomas and Lomen-Hoerth, Catherine and Trojanowski, John Q and McCluskey, Leo and Basak, A. Nazli and Tunca, Ceren and Meitinger, Thomas and Andres, Christian R and Bensimon, Gilbert and Landwehrmeyer, Bernhard and Payan, Christine A. M and Saker-Delye, Safaa and Duerr, Alexandra and Wood, Nicholas W and Rietschel, Marcella and Cichon, Sven and Amouyel, Philippe and Dartigues, Jean-Francois and Uitterlinden, Andre G and Curtis, Charles and de Visser, Marianne and Goris, An and Weber, Markus and Cereda, Cristina and Bertolin, Cinzia and Mazzini, Letizia and Tiloca, Cinzia and Ratti, Antonia and Brunetti, Maura and Capozzo, Rosa and Zecca, Chiara and Lunetta, Christian and Riva, Nilo and Padovani, Alessandro and Muller, Bernard and Stuit, Robbert Jan and Zhang, Katharine and McCann, Emily P and Fifita, Jennifer A and Nicholson, Garth A and Pamphlett, Roger and Grosskreutz, Julian and Prell, Tino and Casale, Federico and Chio, Adrian and Beghi, Ettore and Pupillo, Elisabetta and Tortelli, Rosanna and Logroscino, Giancarlo and Weishaupt, Jochen H and Franke, Lude and Brown, Robert H and Glass, Jonathan D and Landers, John E and Andersen, Peter M and Vourc'h, Patrick and Wray, Naomi R and Visscher, Peter M and van Es, Michael A and Pasterkamp, R. Jeroen and Lewis, Cathryn M and Al-Chalabi, Ammar and van den Berg, Leonard H and Veldink, Jan H
2016, Volume 48, Issue 9
Basic Medicine | Medical Genetics | Medicinsk genetik | Medical and Health Sciences | Medicin och hälsovetenskap | Medicinska och farmaceutiska grundvetenskaper
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