X
Search Filters
Format Format
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
index medicus (25) 25
further section (24) 24
humans (22) 22
female (17) 17
male (16) 16
exhibitions (12) 12
genetics & heredity (8) 8
abridged index medicus (7) 7
adult (7) 7
pediatrics (7) 7
child (6) 6
children (6) 6
adolescent (5) 5
art, modern (5) 5
cardiac & cardiovascular systems (5) 5
child, preschool (5) 5
diagnosis (5) 5
genetic aspects (5) 5
genetics (5) 5
hematology (5) 5
middle aged (5) 5
phenotype (5) 5
society news (5) 5
aged (4) 4
infant (4) 4
management (4) 4
music (4) 4
mutation (4) 4
mutations (4) 4
research (4) 4
stroke (4) 4
usage (4) 4
young adult (4) 4
20th century (3) 3
animals (3) 3
biography (3) 3
care and treatment (3) 3
chromosome deletion (3) 3
criticism and interpretation (3) 3
electronic books (3) 3
epistaxis (3) 3
expositions (3) 3
gene mutations (3) 3
genetic disorders (3) 3
genomics (3) 3
heart (3) 3
heart beat (3) 3
heart diseases (3) 3
internal medicine (3) 3
iron (3) 3
manuscripts (3) 3
oncology (3) 3
pathology (3) 3
patients (3) 3
research article (3) 3
retrospective studies (3) 3
risk factors (3) 3
therapy (3) 3
united states (3) 3
1839-1906 (2) 2
abnormalities (2) 2
abstracts (2) 2
age (2) 2
anticoagulants (2) 2
array comparative genomic hybridization (2) 2
art (2) 2
article (2) 2
artists (2) 2
atrial fibrillation (2) 2
base sequence (2) 2
basel (2) 2
beeldende kunsten (2) 2
bibliography (2) 2
cancer (2) 2
cardiovascular (2) 2
case report (2) 2
catalogs (2) 2
cell cycle (2) 2
cezanne, paul (2) 2
cezanne, paul, 1839-1906 (2) 2
clinical genetics (2) 2
composers (2) 2
congenital heart disease (2) 2
congenital, hereditary, and neonatal diseases and abnormalities (2) 2
consecutive patients (2) 2
cézanne, paul (2) 2
cézanne, paul, 1839-1906 (2) 2
cézanne, paul, 1839-1906 exhibitions (2) 2
death (2) 2
diagnosis, differential (2) 2
diet (2) 2
differential diagnosis (2) 2
diseases (2) 2
epistaxis severity score (2) 2
erratum (2) 2
exhibition catalogs (2) 2
exome - genetics (2) 2
expressionism (2) 2
fibromyalgia (2) 2
fish oils (2) 2
more...
Library Location Library Location
Library Location Library Location
X
Sort by Item Count (A-Z)
Filter by Count
Robarts - Stacks (9) 9
Art - Library use only (5) 5
Music - Stacks (4) 4
Royal Ontario Museum - Stacks (2) 2
UTL at Downsview - May be requested (2) 2
Collection Dvlpm't (Acquisitions) - Closed Orders (1) 1
Music - Protected Material (1) 1
UofT at Mississauga - Stacks (1) 1
UofT at Scarborough - Stacks (1) 1
more...
Language Language
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


Pediatric Blood & Cancer, ISSN 1545-5009, 09/2014, Volume 61, Issue 9, pp. 1701 - 1703
Journal Article
Journal of the Association of Genetic Technologists, ISSN 1523-7834, 2017, Volume 43, Issue 2, p. 56
To the Editor: Partial and whole duplications of the short arm of chromosome 9 have been commonly reported in the literature with characteristic phenotypic... 
Journal Article
Genetics in Medicine, ISSN 1098-3600, 04/2019, Volume 21, Issue 4, pp. 867 - 876
Neurofibromatosis type 1 (NF1) is characterized by a highly variable clinical presentation, but almost all NF1-affected adults present with cutaneous and/or... 
genotype–phenotype correlation | NF1 | p.Met992del | learning difficulties | neurofibroma | GENETICS & HEREDITY
Journal Article
Human Mutation, ISSN 1059-7794, 02/2018, Volume 39, Issue 2, pp. 281 - 291
Journal Article
Genetics in medicine : official journal of the American College of Medical Genetics, ISSN 1098-3600, 03/2019, Volume 21, Issue 3, pp. 764 - 765
A correction has been published to this Article. The PDF and HTML have been updated accordingly. 
Journal Article
Journal Article
by Koczkowska, Magdalena and Callens, Tom and Chen, Yunjia and Gomes, Alicia and Hicks, Alesha D and Sharp, Angela and Johns, Eric and Uhas, Kim Armfield and Armstrong, Linlea and Bosanko, Katherine Armstrong and Babovic‐Vuksanovic, Dusica and Baker, Laura and Basel, Donald G and Bengala, Mario and Bennett, James T and Chambers, Chelsea and Clarkson, Lola K and Clementi, Maurizio and Cortés, Fanny M and Cunningham, Mitch and D'Agostino, M. Daniela and Delatycki, Martin B and Digilio, Maria C and Dosa, Laura and Esposito, Silvia and Fox, Stephanie and Freckmann, Mary‐Louise and Fauth, Christine and Giugliano, Teresa and Giustini, Sandra and Goetsch, Allison and Goldberg, Yael and Greenwood, Robert S and Griffis, Cristin and Gripp, Karen W and Gupta, Punita and Haan, Eric and Hachen, Rachel K and Haygarth, Tamara L and Hernández‐Chico, Concepción and Hodge, Katelyn and Hopkin, Robert J and Hudgins, Louanne and Janssens, Sandra and Keller, Kory and Kelly‐Mancuso, Geraldine and Kochhar, Aaina and Korf, Bruce R and Lewis, Andrea M and Liebelt, Jan and Lichty, Angie and Listernick, Robert H and Lyons, Michael J and Maystadt, Isabelle and Ojeda, Mayra Martinez and McDougall, Carey and McGregor, Lesley K and Melis, Daniela and Mendelsohn, Nancy and Nowaczyk, Malgorzata J.M and Ortenberg, June and Panzer, Karin and Pappas, John G and Pierpont, Mary Ella and Piluso, Giulio and Pinna, Valentina and Pivnick, Eniko K and Pond, Dinel A and Powell, Cynthia M and Rogers, Caleb and Shahar, Noa Ruhrman and Rutledge, S. Lane and Saletti, Veronica and Sandaradura, Sarah A and Santoro, Claudia and Schatz, Ulrich A and Schreiber, Allison and Scott, Daryl A and Sellars, Elizabeth A and Sheffer, Ruth and Siqveland, Elizabeth and Slopis, John M and Smith, Rosemarie and Spalice, Alberto and Stockton, David W and Streff, Haley and Theos, Amy and Tomlinson, Gail E and Tran, Grace and Trapane, Pamela L and Trevisson, Eva and Ullrich, Nicole J and Van den Ende, Jenneke and Schrier Vergano, Samantha A and Wallace, Stephanie E and Wangler, Michael F and Weaver, David D and Yohay, Kaleb H and Zackai, Elaine and Zonana, Jonathan and ...
Human Mutation, ISSN 1059-7794, 10/2019
Journal Article
Journal Article
Journal of Pediatric Genetics, ISSN 2146-4596, 03/2018, Volume 7, Issue 1, pp. 023 - 028
Abstract We report a 19-year-old female patient with a history of short stature, primary ovarian insufficiency, sensorineural hearing loss, sacral teratoma,... 
Case Report | fluorescence in situ hybridization | translocation | atypical Turner's syndrome | array comparative genomic hybridization | 3q25.33-q29 duplication | functional disomy Xp | Xq13.2-q28 deletion | duplication 3q syndrome | XIST | intellectual disability
Journal Article
Journal of Pediatric Genetics, ISSN 2146-4596, 03/2018, Volume 7, Issue 1, pp. 035 - 039
Abstract We report a 4-month-old male proband with a history of prominent forehead, hypertelorism, ear abnormalities, micrognathia, hypospadias, and multiple... 
Case Report | fluorescence in situ hybridization | unbalanced translocation | array comparative genomic hybridization | 13q33.2-q34 deletion | double balanced translocation carrier | 7p21.3-p22.3 duplication
Journal Article
Journal Article
Journal Article
Journal Article