X
Search Filters
Format Format
Format Format
X
Sort by Item Count (A-Z)
Filter by Count
Journal Article (1702) 1702
Publication (255) 255
Book Chapter (17) 17
Book Review (8) 8
Magazine Article (3) 3
Conference Proceeding (2) 2
Dissertation (2) 2
Book / eBook (1) 1
Web Resource (1) 1
more...
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
humans (1468) 1468
female (958) 958
male (879) 879
index medicus (753) 753
digeorge syndrome - genetics (618) 618
child (575) 575
chromosome deletion (523) 523
digeorge syndrome (515) 515
digeorge syndrome - diagnosis (465) 465
adolescent (450) 450
genetics & heredity (410) 410
adult (401) 401
velocardiofacial syndrome (393) 393
infant (369) 369
phenotype (352) 352
digeorge-syndrome (348) 348
child, preschool (343) 343
infant, newborn (343) 343
cardio-facial syndrome (334) 334
chromosomes, human, pair 22 - genetics (321) 321
pediatrics (313) 313
children (291) 291
chromosomes, human, pair 22 (289) 289
digeorge syndrome - complications (287) 287
schizophrenia (255) 255
22q11.2 deletion syndrome (249) 249
in situ hybridization, fluorescence (215) 215
heart defects, congenital - genetics (200) 200
psychiatry (175) 175
syndrome (171) 171
article (169) 169
young adult (167) 167
diagnosis (162) 162
genetic disorders (149) 149
abnormalities, multiple - genetics (148) 148
pregnancy (146) 146
defects (142) 142
prevalence (139) 139
congenital heart disease (130) 130
retrospective studies (129) 129
research (119) 119
analysis (118) 118
immunology (118) 118
digeorge syndrome - psychology (114) 114
adolescents (113) 113
genetics (110) 110
digeorge syndrome - pathology (109) 109
gene deletion (109) 109
risk factors (109) 109
digeorge syndrome - immunology (108) 108
genetic aspects (104) 104
microdeletions (104) 104
digeorge syndrome - physiopathology (100) 100
neurosciences (99) 99
spectrum (97) 97
digeorge (96) 96
22q11 deletion syndrome (95) 95
heart defects, congenital - diagnosis (95) 95
adults (94) 94
immunodeficiency (94) 94
diagnosis, differential (93) 93
chromosomes (92) 92
anomalies (91) 91
middle aged (90) 90
animals (89) 89
deletion (89) 89
digeorge syndrome - epidemiology (89) 89
22q11.2 deletion (87) 87
microdeletion (87) 87
cardiac & cardiovascular systems (86) 86
abnormalities, multiple - diagnosis (85) 85
patients (84) 84
chromosome 22q11 (83) 83
mutation (83) 83
surgery (83) 83
clinical neurology (82) 82
psychosis (82) 82
22q11 (81) 81
22q11 deletion (81) 81
clinical-features (79) 79
abridged index medicus (76) 76
genotype (76) 76
prenatal diagnosis (76) 76
care and treatment (75) 75
disorders (75) 75
chromosome 22 (74) 74
tbx1 (74) 74
magnetic resonance imaging (72) 72
genes (70) 70
health aspects (70) 70
immunological deficiency syndromes (69) 69
mice (69) 69
velo-cardio-facial syndrome (69) 69
medicine & public health (68) 68
mental disorders (68) 68
congenital heart-disease (66) 66
gene (66) 66
disease (65) 65
schizophrenia - genetics (65) 65
cardio-facial-syndrome (64) 64
more...
Language Language
Language Language
X
Sort by Item Count (A-Z)
Filter by Count
English (1593) 1593
French (30) 30
German (22) 22
Spanish (20) 20
Japanese (10) 10
Chinese (8) 8
Portuguese (8) 8
Italian (6) 6
Russian (5) 5
Danish (4) 4
Polish (4) 4
Korean (3) 3
Hungarian (2) 2
Norwegian (2) 2
Serbian (2) 2
Swedish (2) 2
Dutch (1) 1
Hebrew (1) 1
Romanian (1) 1
Slovak (1) 1
more...
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


Pediatric Clinics of North America, ISSN 0031-3955, 2015, Volume 62, Issue 2, pp. 411 - 426
Journal Article
Journal of Intellectual Disability Research, ISSN 0964-2633, 04/2015, Volume 59, Issue 4, pp. 307 - 318
Background There are a number of neurogenetic syndromes with well described behavioural phenotypes including fragile X syndrome, Prader–Willi syndrome,... 
ADHD | autism spectrum disorder (ASD) | Prader–Willi syndrome | velo‐cardio‐facial syndrome (VCFS) | fragile X syndrome | Williams syndrome | Velo-cardio-facial syndrome (VCFS) | Fragile X syndrome | Autism spectrum disorder (ASD) | Prader-Willi syndrome | 22Q11.2 DELETION | ATTENTION | velo-cardio-facial syndrome (VCFS) | PREVALENCE | AUTISM SPECTRUM DISORDERS | PERVASIVE DEVELOPMENTAL DISORDERS | EDUCATION, SPECIAL | FRAGILE-X-SYNDROME | PSYCHIATRIC-DISORDERS | VELOCARDIOFACIAL SYNDROME | REHABILITATION | PRADER-WILLI-SYNDROME | YOUNG-CHILDREN | Humans | Parents | Child, Preschool | Male | Fragile X Syndrome - drug therapy | Young Adult | Ireland | Adult | Female | Attention Deficit Disorder with Hyperactivity - diagnosis | Mental Disorders - diagnosis | Child | Autism Spectrum Disorder - diagnosis | DiGeorge Syndrome - drug therapy | Prader-Willi Syndrome - drug therapy | Health Care Surveys - methods | Prader-Willi Syndrome - diagnosis | Williams Syndrome - drug therapy | United Kingdom | Attention Deficit Disorder with Hyperactivity - drug therapy | Syndrome | Williams Syndrome - diagnosis | DiGeorge Syndrome - diagnosis | Mental Disorders - drug therapy | Psychopharmacology | Adolescent | Autism Spectrum Disorder - drug therapy | Health Care Surveys - statistics & numerical data | Fragile X Syndrome - diagnosis | Psychological aspects | Surveys | Health aspects | Mental health | Attention-deficit hyperactivity disorder | Disabled children | Mental disorders | Hyperactivity | Attention Deficit Hyperactivity Disorder
Journal Article
Journal of the American Academy of Child & Adolescent Psychiatry, ISSN 0890-8567, 2009, Volume 48, Issue 11, pp. 1060 - 1068
Abstract Objective Velocardiofacial syndrome (VCFS) is associated with cognitive deficits and high rates of schizophrenia and other neuropsychiatric disorders.... 
Pediatrics | Psychiatry | 22q11.2 deletion syndrome | depression mood disorders | Verbal IQ | schizophrenia | neurodevelopmental disorder | PSYCHIATRY | FORMAL THOUGHT-DISORDER | PSYCHOLOGY, DEVELOPMENTAL | SPECTRUM DISORDERS | RISK | OBSESSIVE-COMPULSIVE DISORDER | CHILDREN | ADOLESCENTS | PEDIATRICS | CHILDHOOD-ONSET SCHIZOPHRENIA | K-SADS-PL | PSYCHOPATHOLOGY | CARDIO-FACIAL SYNDROME | Intelligence | Young Adults | Schizophrenia | Scores | Foreign Countries | Europe (West) | Patients | Cognitive Development | Intelligence Tests | Tests | Depression (Psychology) | Children | Evaluation Methods | Israel | Longitudinal Studies | Age | Symptoms (Individual Disorders) | Humans | Middle Aged | Child, Preschool | Male | Schizophrenic Psychology | Intellectual Disability - genetics | Young Adult | Language Development Disorders - psychology | Mental Disorders - genetics | Schizophrenia - genetics | Schizophrenia - diagnosis | Language Development Disorders - diagnosis | Adult | Female | Mental Disorders - diagnosis | Child | DiGeorge Syndrome - genetics | Wechsler Scales - statistics & numerical data | Psychotic Disorders - diagnosis | Comorbidity | Language Development Disorders - genetics | Psychotic Disorders - psychology | Psychometrics | DiGeorge Syndrome - psychology | Switzerland | Mental Disorders - psychology | Phenotype | Psychotic Disorders - genetics | DiGeorge Syndrome - diagnosis | Cross-Cultural Comparison | Intellectual Disability - diagnosis | Adolescent | Intellectual Disability - psychology | Psychological aspects | Research | Child development | Child psychopathology | Intelligence tests | Genetic disorders | Mental depression
Journal Article
Journal of Thrombosis and Haemostasis, ISSN 1538-7933, 02/2019, Volume 17, Issue 2, pp. 295 - 305
Journal Article
Journal of Pediatrics, The, ISSN 0022-3476, 2014, Volume 164, Issue 6, pp. 1475 - 1480.e2
Journal Article
Developmental Disabilities Research Reviews, ISSN 1940-5510, 2008, Volume 14, Issue 1, pp. 3 - 10
Journal Article
American Journal of Medical Genetics Part A, ISSN 1552-4825, 04/2017, Volume 173, Issue 4, pp. 879 - 888
Journal Article
Schizophrenia Bulletin, ISSN 0586-7614, 09/2017, Volume 43, Issue 5, pp. 1079 - 1089
Journal Article
Journal Article