X
Search Filters
Format Format
Format Format
X
Sort by Item Count (A-Z)
Filter by Count
Journal Article (129) 129
Newspaper Article (54) 54
Publication (29) 29
Book / eBook (16) 16
Magazine Article (15) 15
Book Review (5) 5
Dissertation (5) 5
Patent (5) 5
Book Chapter (2) 2
Conference Proceeding (2) 2
Web Resource (1) 1
more...
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
humans (66) 66
genetics & heredity (52) 52
index medicus (47) 47
male (45) 45
female (43) 43
child (27) 27
genetics (22) 22
mutation (22) 22
article (21) 21
adolescent (20) 20
genetic aspects (20) 20
child, preschool (19) 19
phenotype (18) 18
infant (16) 16
research (16) 16
animals (15) 15
genes (15) 15
military personnel (14) 14
adult (13) 13
autism (13) 13
infant, newborn (13) 13
gene (11) 11
intellectual disability - genetics (10) 10
proteins (10) 10
risk factors (10) 10
abnormalities, multiple - genetics (9) 9
comparative genomic hybridization (9) 9
genomes (9) 9
genotype (9) 9
life sciences (9) 9
mental-retardation (9) 9
mice (9) 9
chromosome deletion (8) 8
cohort studies (8) 8
expression (8) 8
genetic predisposition to disease (8) 8
genomics (8) 8
intellectual disabilities (8) 8
mental disorders (8) 8
mutations (8) 8
alleles (7) 7
biochemistry & molecular biology (7) 7
genome-wide association (7) 7
genome-wide association study (7) 7
intellectual disability (7) 7
medicine (7) 7
molecular sequence data (7) 7
polymorphism, single nucleotide (7) 7
pregnancy (7) 7
transcription factors - genetics (7) 7
[sdv.gen]life sciences [q-bio]/genetics (6) 6
analysis (6) 6
armed forces (6) 6
clonal deletion (6) 6
developmental disabilities - genetics (6) 6
diagnosis (6) 6
dna copy number variations (6) 6
gene deletion (6) 6
gene mutations (6) 6
health aspects (6) 6
history (6) 6
social networks (6) 6
[ sdv.gen ] life sciences [q-bio]/genetics (5) 5
behavior (5) 5
children (5) 5
chromosomes (5) 5
deletions (5) 5
disease (5) 5
genetic variation (5) 5
human necessities (5) 5
internet (5) 5
mental retardation (5) 5
microcephaly - genetics (5) 5
pedigree (5) 5
studies (5) 5
web sites (5) 5
young adult (5) 5
abnormalities, multiple - pathology (4) 4
aged (4) 4
amino acid sequence (4) 4
association (4) 4
automobile dealers (4) 4
automobile industry (4) 4
bandages, dressings or absorbent pads (4) 4
bmd (4) 4
bone density - genetics (4) 4
canadians (4) 4
cell cycle (4) 4
chromosomes, human, pair 16 - genetics (4) 4
chromosomes, human, x - genetics (4) 4
craniosynostosis (4) 4
devices providing patency to, or preventing collapsing of,tubular structures of the body, e.g. stents (4) 4
electronic books (4) 4
endocrinology & metabolism (4) 4
exons (4) 4
facies (4) 4
filters implantable into blood vessels (4) 4
first-aid kits (4) 4
fomentation (4) 4
friendly fire (4) 4
more...
Library Location Library Location
Library Location Library Location
X
Sort by Item Count (A-Z)
Filter by Count
Robarts - Stacks (8) 8
UofT at Mississauga - Stacks (7) 7
UofT at Scarborough - Stacks (6) 6
UTL at Downsview - May be requested (4) 4
Collection Dvlpm't (Acquisitions) - Closed Orders (2) 2
Collection Dvlpm't (Acquisitions) - Vendor file (2) 2
Earth Sciences (Noranda) - Stacks (2) 2
Royal Ontario Museum - Stacks (2) 2
Trinity College (John W Graham) - Stacks (2) 2
Victoria University E.J. Pratt - Stacks (2) 2
Earth Sciences (Noranda) - Missing (1) 1
Gerstein Science - Stacks (1) 1
Music - Stacks (1) 1
Online Resources - Online (1) 1
Robarts - Searching (1) 1
Royal Ontario Museum - Far Eastern Egyptian (1) 1
St. Michael's College (John M. Kelly) - 2nd Floor (1) 1
Victoria University CRRS - Library use only (1) 1
more...
Language Language
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


Human Mutation, ISSN 1059-7794, 08/2019, Volume 40, Issue 8, pp. 1013 - 1029
SATB2 ‐associated syndrome (SAS) is an autosomal dominant neurodevelopmental disorder caused by alterations in the SATB2 gene. Here we present a review of... 
associated syndrome | genotype‐phenotype correlation | pathogenic variants | SATB2 | whole exome sequencing | SATB2-associated syndrome | genotype-phenotype correlation | GENETICS & HEREDITY | Genetic aspects | Codon | Genes | Analysis | Animal models | Phenotypes | Reviews | Nonsense mutation | Coding | Stop codon | Neurodevelopmental disorders | Genotypes | Hereditary diseases
Journal Article
by Gillberg, Christopher and Kolevzon, Alexander and Nelson, Stanley F and Sansom, Katherine and Casallo, Guillermo and Miller, Judith and Brennan, Sean and Leboyer, Marion and Bacchelli, Elena and Delorme, Richard and Fombonne, Eric and Hallmayer, Joachim and Green, Jonathan and Pickles, Andrew and Heron, Elizabeth A and Salt, Jeff and Battaglia, Agatino and Klauck, Sabine M and McDougle, Christopher J and Mahoney, William and Noor, Abdul and Cytrynbaum, Cheryl and Sato, Daisuke and Almeida, Joana and Korvatska, Olena and Dawson, Geraldine and Bierut, Laura J and Coon, Hilary and Rickaby, Jessica and Freitag, Christine M and Roeder, Kathryn and Bader, Gary D and Wijsman, Ellen M and Vincent, John B and Hakonarson, Hakon and Segurado, Ricardo and Paton, Tara and Roge, Bernadette and Ennis, Sean and Kim, Cecilia and Monaco, Anthony P and Paterson, Andrew D and Crossett, Andrew and McGrath, Jane and Carson, Andrew R and Le Couteur, Ann and Cook, Edwin H and Chung, Brian H.Y and Cuccaro, Michael L and Van Engeland, Herman and Conroy, Judith and Holt, Richard and Strawbridge, Christina and Kustanovich, Vlad and Migita, Ohsuke and Stoppioni, Vera and Igliozzi, Roberta and Poustka, Fritz and Stein, Olaf and Posey, David J and Sheffield, Val C and Duque, Frederico and Parrini, Barbara and Berney, Tom and Hus, Vanessa and Baird, Gillian and Duketis, Eftichia and Soorya, Latha and Corsello, Christina and Drmic, Irene and Sousa, Inês and Abrahams, Brett S and Thomson, Susanne and Lajonchere, Clara M and Tsiantis, John and Pinto, Dalila and Green, Andrew and Hughes, Gillian and Mantoulan, Carine and Betancur, Catalina and Volkmar, Fred and Poustka, Annemarie and Shah, Naisha and Bryson, Susan E and Munson, Jeff and Tancredi, Raffaella and Nygren, Gudrun and Wittemeyer, Kerstin and Merikangas, Alison and Oliveira, Guiomar and Farrar, Penny and Maestrini, Elena and Liu, Xiao-Qing and Gallagher, Louise and McConachie, Helen and Zurawiecki, Danielle and Schellenberg, Gerard D and Glessner, Joseph T and Lord, Catherine and Piven, Joseph and ... and Sahlgrenska akademin and Institutionen för neurovetenskap och fysiologi, sektionen för psykiatri och neurokemi and Göteborgs universitet and Gothenburg University and Institute of Neuroscience and Physiology, Department of Psychiatry and Neurochemistry and Sahlgrenska Academy
Nature, ISSN 0028-0836, 07/2010, Volume 466, Issue 7304, pp. 368 - 372
Journal Article
Human Genetics, ISSN 0340-6717, 2016, Volume 135, Issue 5, pp. 569 - 586
Journal Article
Journal Article
by Neale, Benjamin M and Neale, Benjamin M and Kou, Yan and Samocha, Kaitlin E and Liu, Li and Lim, Elaine and Ma'Ayan, Avi and Rossin, Elizabeth and Samocha, Kaitlin E and Kirby, Andrew and Fromer, Menachem and Sabo, Aniko and Lin, Chiao-Feng and Daly, Mark J and Stevens, Christine and Rossin, Elizabeth and Kirby, Andrew and Wang, Li-San and Makarov, Vladimir and Flannick, Jason and Polak, Paz and Fromer, Menachem and Shakir, Khalid and Yoon, Seungtai and Maguire, Jared and Fennell, Tim and Garimella, Kiran and Crawford, Emily L and Banks, Eric and Campbell, Nicholas G and Poplin, Ryan and Geller, Evan T and Valladares, Otto and Gabriel, Stacey and Schafer, Chad and De Pristo, Mark and Sunyaev, Shamil and Liu, Han and Daly, Mark J and Zhao, Tuo and Cai, Guiqing and Lihm, Jayon and Dannenfelser, Ruth and Jabado, Omar and Peralta, Zuleyma and Nagaswamy, Uma and Muzny, Donna and Reid, Jeffrey G and Newsham, Irene and Wu, Yuanqing and Lewis, Lora and Han, Yi and Voight, Benjamin F and Lim, Elaine and Rossin, Elizabeth and Kirby, Andrew and Flannick, Jason and Fromer, Menachem and Shakir, Khalid and Fennell, Tim and Garimella, Kiran and Banks, Eric and Poplin, Ryan and Gabriel, Stacey and Depristo, Mark and Wimbish, Jack R and Boone, Braden E and Levy, Shawn E and Betancur, Catalina and Sunyaev, Shamil and Boerwinkle, Eric and Buxbaum, Joseph D and Cook Jr, Edwin H and Devlin, Bernie and Gibbs, Richard A and Roeder, Kathryn and Schellenberg, Gerard D and Sutcliffe, James S and Daly, Mark J
Nature, ISSN 0028-0836, 05/2012, Volume 484, Issue 7397, pp. 242 - 246
Journal Article
Journal of Medical Genetics, ISSN 0022-2593, 05/2010, Volume 47, Issue 5, pp. 332 - 341
Journal Article
Genome Medicine, ISSN 1756-994X, 02/2019, Volume 11, Issue 1, pp. 12 - 17
Journal Article