X
Search Filters
Format Format
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
clonal deletion (13) 13
genetics & heredity (12) 12
diagnosis (8) 8
heart diseases (8) 8
22q11.2 deletion syndrome (7) 7
children (7) 7
coronary artery disease (7) 7
digeorge syndrome (6) 6
index medicus (6) 6
article (5) 5
genetic disorders (5) 5
prevalence (5) 5
velocardiofacial syndrome (5) 5
chromosome deletion (4) 4
congenital diseases (4) 4
congenital heart disease (4) 4
digeorge syndrome - genetics (4) 4
digeorge-syndrome (4) 4
geosciences, multidisciplinary (4) 4
history (4) 4
humans (4) 4
neonates (4) 4
pacific (4) 4
22q11.2ds (3) 3
autism (3) 3
carbonates (3) 3
cardio-facial syndrome (3) 3
cardiovascular disease (3) 3
chromosome 22 (3) 3
chromosome 22q11 (3) 3
chromosomes, human, pair 22 (3) 3
clinical-features (3) 3
congenital heart-disease (3) 3
gene deletion (3) 3
geschichte (3) 3
heart (3) 3
hypocalcemia (3) 3
medical research (3) 3
medicine, experimental (3) 3
nonprofit organizations (3) 3
oceanography (3) 3
paleontology (3) 3
patients (3) 3
pediatrics (3) 3
phenotypic variations (3) 3
thymic hypoplasia (3) 3
variability (3) 3
20th century (2) 2
22q11 deletion syndrome (2) 2
accounting firms (2) 2
acquisitions & mergers (2) 2
adults (2) 2
advertising agencies (2) 2
age (2) 2
analysis (2) 2
animals (2) 2
appointments & personnel changes (2) 2
associations (2) 2
attorneys (2) 2
aufsatzsammlung (2) 2
biochemistry & molecular biology (2) 2
boards of directors (2) 2
call centers (2) 2
casinos (2) 2
chairman of the board (2) 2
chambers of commerce (2) 2
chief executive officers (2) 2
chief operating officers (2) 2
chromosomes (2) 2
cleft lip/palate (2) 2
climate-change (2) 2
clubfoot (2) 2
commercial loan officers (2) 2
commercial real estate (2) 2
community banks (2) 2
construction companies (2) 2
corporate headquarters (2) 2
corporate profiles (2) 2
credit managers (2) 2
credit unions (2) 2
design (2) 2
digeorge syndrome - diagnosis (2) 2
directors (2) 2
disease (2) 2
disorders (2) 2
entrepreneurs (2) 2
epidemiology (2) 2
executives (2) 2
female (2) 2
fetuses (2) 2
financial management (2) 2
financial statements (2) 2
general contractors (2) 2
growth (2) 2
guidelines (2) 2
haploinsufficiency (2) 2
health risk assessment (2) 2
histoire (2) 2
home repair & remodeling (2) 2
hospitals (2) 2
more...
Library Location Library Location
Library Location Library Location
X
Sort by Item Count (A-Z)
Filter by Count
Robarts - Stacks (6) 6
Trinity College (John W Graham) - Storage (2) 2
UTL at Downsview - May be requested (2) 2
UofT at Mississauga - Stacks (2) 2
Collection Dvlpm't (Acquisitions) - Closed Orders (1) 1
Collection Dvlpm't (Acquisitions) - Vendor file (1) 1
Royal Ontario Museum - Stacks (1) 1
St. Michael's College (John M. Kelly) - 2nd Floor (1) 1
UofT at Scarborough - Stacks (1) 1
Victoria University E.J. Pratt - Stacks (1) 1
more...
Language Language
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


American Journal of Medical Genetics Part A, ISSN 1552-4825, 03/2019, Volume 179, Issue 3, pp. 381 - 385
The 22q11.2 deletion syndrome (22q11.2DS) involves multiple organ systems with variable phenotypic expression. Genitourinary tract abnormalities have been... 
22q11.2 deletion syndrome | renal | genitourinary | DiGeorge syndrome | pediatrics | urology | DIGEORGE-SYNDROME | MALFORMATIONS | GENETICS & HEREDITY | SPECTRUM | Kidneys | Clonal deletion | Etiology | Cryptorchidism | Urinary tract | Children | Diagnosis | Genitourinary tract
Journal Article
American journal of medical genetics. Part A, 12/2018
The 22q11.2 deletion syndrome (22q11.2DS) involves multiple organ systems with variable phenotypic expression. Genitourinary tract abnormalities have been... 
Journal Article
by Lopez-Rivera, Esther and Liu, Qingxue and Liu, Yangfan P and Verbitsky, Miguel and Anderson, Blair R and Capone, Valentina P and Otto, Edgar A and Yan, Zhonghai and Mitrotti, Adele and Martino, Jeremiah and Steers, Nicholas J and Fasel, David A and Vukojevic, Katarina and Deng, Rong and Racedo, Silvia E and Werth, Max and Westland, Rik and Vivante, Asaf and Makar, Gabriel S and Bodria, Monica and Sampson, Matthew G and Gillies, Christopher E and Vega-Warner, Virginia and Maiorana, Mariarosa and Petrey, Donald S and Honig, Barry and Lozanovski, Vladimir J and Salomon, Rémi and Heidet, Laurence and Carpentier, Wassila and Gaillard, Dominique and Carrea, Alba and Gesualdo, Loreto and Cusi, Daniele and Izzi, Claudia and Scolari, Francesco and van Wijk, Joanna A.E and Arapovic, Adela and Saraga-Babic, Mirna and Saraga, Marijan and Kunac, Nenad and Samii, Ali and McDonald-McGinn, Donna M and Crowley, Terrence B and Zackai, Elaine H and Drozdz, Dorota and Miklaszewska, Monika and Tkaczyk, Marcin and Sikora, Przemyslaw and Szczepanska, Maria and Mizerska-Wasiak, Malgorzata and Krzemien, Grazyna and Szmigielska, Agnieszka and Zaniew, Marcin and Darlow, John M and Puri, Prem and Barton, David and Casolari, Emilio and Furth, Susan L and Warady, Bradley A and Gucev, Zoran and Hakonarson, Hakon and Flogelova, Hana and Tasic, Velibor and Latos-Bielenska, Anna and Materna-Kiryluk, Anna and Allegri, Landino and Wong, Craig S and Drummond, Iain A and D’Agati, Vivette and Imamoto, Akira and Barasch, Jonathan M and Hildebrandt, Friedhelm and Kiryluk, Krzysztof and Lifton, Richard P and Morrow, Bernice E and Jeanpierre, Cecile and Papaioannou, Virginia E and Ghiggeri, Gian Marco and Gharavi, Ali G and Katsanis, Nicholas and Sanna-Cherchi, Simone
The New England Journal of Medicine, ISSN 0028-4793, 02/2017, Volume 376, Issue 8, pp. 742 - 754
Journal Article
Journal Article
American Journal of Medical Genetics, Part A, ISSN 1552-4825, 10/2018, Volume 176, Issue 10, pp. 2135 - 2139
The 22q11.2 Deletion Syndrome (22q11.2DS) occurs in similar to 1:3,000-6,000 individuals. Features less typically associated with 22q11.2DS, such as orthopedic... 
22q11.2 deletion syndrome | orthopedics | pes equinovarus | 22q11.2DS | club foot | clubfoot | POPULATION | GUIDELINES | GENETICS & HEREDITY | PREVALENCE | EPIDEMIOLOGY | INFANCY | Medicine, Experimental | Medical research | Congenital heart disease | Genetic disorders | Clubfoot | Neonates | Clonal deletion | Diagnosis | Patients | Heart diseases | Coronary artery disease | Feet | Cleft lip/palate | Original
Journal Article
Journal Article
American Journal of Medical Genetics Part A, ISSN 1552-4825, 10/2018, Volume 176, Issue 10, pp. 2172 - 2181
Journal Article