X
Search Filters
Format Format
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
humans (76) 76
female (60) 60
genetics & heredity (57) 57
male (51) 51
index medicus (41) 41
adult (32) 32
pregnancy (31) 31
infant, newborn (26) 26
phenotype (23) 23
child (21) 21
child, preschool (18) 18
prevalence (18) 18
registries (16) 16
adolescent (15) 15
mutation (15) 15
biochemistry & molecular biology (14) 14
europe - epidemiology (14) 14
congenital abnormalities - epidemiology (13) 13
epidemiology (13) 13
infant (13) 13
genetics (12) 12
abnormalities, multiple - genetics (11) 11
congenital defects (11) 11
gene (10) 10
phytochelatins (10) 10
article (9) 9
cadmium (9) 9
chemistry, analytical (9) 9
intellectual disability - genetics (9) 9
phaeodactylum tricornutum (9) 9
syndrome (9) 9
birth (8) 8
cohort studies (8) 8
international cooperation (8) 8
mental-retardation (8) 8
population surveillance - methods (8) 8
prenatal diagnosis (8) 8
young adult (8) 8
age (7) 7
americas - epidemiology (7) 7
australia - epidemiology (7) 7
china - epidemiology (7) 7
congenital abnormalities - pathology (7) 7
copper (7) 7
dna mutational analysis (7) 7
epidemiologic studies (7) 7
genetic aspects (7) 7
italy (7) 7
maternal age (7) 7
medicine (7) 7
mutations (7) 7
pedigree (7) 7
population surveillance (7) 7
research (7) 7
risk factors (7) 7
abnormalities, multiple - epidemiology (6) 6
abnormalities, multiple - pathology (6) 6
biomedical research - trends (6) 6
chromosomes (6) 6
data processing (6) 6
facies (6) 6
genes (6) 6
glutathione (6) 6
heart (6) 6
malformations (6) 6
pediatrics (6) 6
population (6) 6
abnormalities, multiple (5) 5
case-control studies (5) 5
defects (5) 5
europe (5) 5
genetic association studies (5) 5
genetic disorders (5) 5
intellectual disability (5) 5
metal-binding peptides (5) 5
middle aged (5) 5
obstetrics & gynecology (5) 5
peptides (5) 5
physiological aspects (5) 5
proteins (5) 5
public health (5) 5
reviews (5) 5
toxicology (5) 5
women (5) 5
abnormalities, multiple - diagnosis (4) 4
analysis (4) 4
anomalies (4) 4
complexes (4) 4
congenital diseases (4) 4
congenital malformations (4) 4
delineation (4) 4
diagnosis (4) 4
diagnosis, differential (4) 4
fortification (4) 4
gene mutations (4) 4
genetic counseling (4) 4
genotype (4) 4
hand deformities, congenital - genetics (4) 4
haploinsufficiency (4) 4
higher-plants (4) 4
more...
Library Location Library Location
Language Language
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


BMJ : British Medical Journal, ISSN 0959-8138, 5/2015, Volume 350, Issue may14 10, pp. h2518 - h2518
Journal Article
European Journal of Human Genetics, ISSN 1018-4813, 08/2014, Volume 22, Issue 8, pp. 1026 - 1033
Journal Article
Human Mutation, ISSN 1059-7794, 07/2014, Volume 35, Issue 7, pp. 841 - 850
Journal Article
Case reports in medicine, ISSN 1687-9627, 2019, Volume 2019, pp. 6317956 - 5
Mast cells are abundant in the heart, among myocardial fibers, around coronary arteries, within arterial intima and intramural vessels, and in atherosclerotic... 
Heart | Myocardial ischemia | Cardiovascular disease | Emergency medical care | Family medical history | Angina | Ultrasonic imaging | Anaphylaxis | Immunology | Pain | Ischemia | Atherosclerosis | Blood pressure | Plaques | Medical imaging | Consciousness | Urticaria | Hypersensitivity | Coronary artery | Angina pectoris | Thrombosis | Allergies | Arteriosclerosis | Coronary vessels | Venom | Tryptase | Biomarkers | Mast cells
Journal Article
Plant Science, ISSN 0168-9452, 2004, Volume 167, Issue 2, pp. 289 - 296
The cellular defence mechanisms used by the marine diatom Phaeodactylum tricornutum to cope with copper toxicity were investigated. Copper induced a rapid... 
Phaeodactylum tricornutum | Phytochelatins | Microalgae | Thiols | Copper | Antioxidant enzymes
Journal Article
Journal Article
Italian Journal of Pediatrics, ISSN 1720-8424, 07/2016, Volume 42, Issue 1, p. 65
Background: Women in many countries are advised to use folic acid supplements before and early during pregnancy to reduce the risk of neural tube defects in... 
Pregnancy | Italy | Supplementation | Neural tube defects | Folic acid | Predictors | POPULATION | NEURAL-TUBE DEFECTS | CANCER | WOMEN | REDUCTION | PEDIATRICS | FORTIFICATION | FOLATE | Prevalence | Cross-Sectional Studies | Humans | Adult | Female | Neural Tube Defects - prevention & control | Surveys and Questionnaires | Dietary Supplements | Folic Acid - administration & dosage | Preconception Care
Journal Article
by Ivanovski, Ivan and Djuric, Olivera and Caraffi, Stefano Giuseppe and Santodirocco, Daniela and Pollazzon, Marzia and Rosato, Simonetta and Cordelli, Duccio Maria and Abdalla, Ebtesam and Accorsi, Patrizia and Adam, Margaret P and Ajmone, Paola Francesca and Badura-Stronka, Magdalena and Baldo, Chiara and Baldi, Maddalena and Bayat, Allan and Bigoni, Stefania and Bonvicini, Federico and Breckpot, Jeroen and Callewaert, Bert and Cocchi, Guido and Cuturilo, Goran and De Brasi, Daniele and Devriendt, Koenraad and Dinulos, Mary Beth and Hjortshøj, Tina Duelund and Epifanio, Roberta and Faravelli, Francesca and Fiumara, Agata and Formisano, Debora and Giordano, Lucio and Grasso, Marina and Grønborg, Sabine and Iodice, Alessandro and Iughetti, Lorenzo and Kuburovic, Vladimir and Kutkowska-Kazmierczak, Anna and Lacombe, Didier and Lo Rizzo, Caterina and Luchetti, Anna and Malbora, Baris and Mammi, Isabella and Mari, Francesca and Montorsi, Giulia and Moutton, Sebastien and Møller, Rikke S and Muschke, Petra and Nielsen, Jens Erik Klint and Obersztyn, Ewa and Pantaleoni, Chiara and Pellicciari, Alessandro and Pisanti, Maria Antonietta and Prpic, Igor and Poch-Olive, Maria Luisa and Raviglione, Federico and Renieri, Alessandra and Ricci, Emilia and Rivieri, Francesca and Santen, Gijs W and Savasta, Salvatore and Scarano, Gioacchino and Schanze, Ina and Selicorni, Angelo and Silengo, Margherita and Smigiel, Robert and Spaccini, Luigina and Sorge, Giovanni and Szczaluba, Krzysztof and Tarani, Luigi and Tone, Luis Gonzaga and Toutain, Annick and Trimouille, Aurelien and Valera, Elvis Terci and Vergano, Samantha Schrier and Zanotta, Nicoletta and Zenker, Martin and Conidi, Andrea and Zollino, Marcella and Rauch, Anita and Zweier, Christiane and Garavelli, Livia
Genetics in Medicine, ISSN 1098-3600, 09/2018, Volume 20, Issue 9, pp. 965 - 975
Journal Article
American Journal of Medical Genetics Part A, ISSN 1552-4825, 11/2018, Volume 176, Issue 11, pp. 2501 - 2508
Wolf–Hirschhorn syndrome is a well‐defined disorder due to 4p16.3 deletion, characterized by distinct facial features, intellectual disability, prenatal and... 
mir‐943 | Wolf–Hirschhorn syndrome | gene | CHD | NSD2 | NSD2 gene | mir-943 | DEFECT | PHENOTYPE | WOLF-HIRSCHHORN-SYNDROME | LETM1 | SEIZURES | DOWN-SYNDROME | GENETICS & HEREDITY | NKX2-5 | Wolf-Hirschhorn syndrome | CRITICAL REGION | Coronary heart disease | Seizures (Medicine) | Literature reviews | Phenotypes | Microencephaly | Growth rate | Clonal deletion | Pathogenesis | Physical growth | Mental retardation | Growth disorders | Genotypes | Seizures
Journal Article
International Journal of Environmental Research and Public Health, ISSN 1661-7827, 03/2017, Volume 14, Issue 3, p. 292
Journal Article
American Journal of Medical Genetics Part A, ISSN 1552-4825, 04/2012, Volume 158A, Issue 4, pp. 917 - 921
Bohring–Opitz syndrome (BOS) is a rare condition characterized by facial anomalies, multiple malformations, failure to thrive and severe intellectual... 
ASXL1 | gene | genotype–phenotype correlations | Bohring–Opitz syndrome | genotype-phenotype correlations | Bohring-Opitz syndrome | ADDITIONAL-SEX-COMBS-LIKE-1 | MYELOID-LEUKEMIA | ASXL1 gene | GENETICS & HEREDITY | Genotype-phenotype correlations
Journal Article
Genetics in Medicine, ISSN 1098-3600, 06/2017, Volume 19, Issue 6, pp. 691 - 700