X
Search Filters
Format Format
Format Format
X
Sort by Item Count (A-Z)
Filter by Count
Journal Article (12595) 12595
Book Review (1516) 1516
Publication (1276) 1276
Book / eBook (382) 382
Newsletter (133) 133
Newspaper Article (99) 99
Book Chapter (75) 75
Conference Proceeding (28) 28
Dissertation (27) 27
Trade Publication Article (24) 24
Magazine Article (14) 14
Reference (9) 9
Data Set (2) 2
Government Document (2) 2
Transcript (1) 1
more...
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
index medicus (10819) 10819
humans (9347) 9347
male (6412) 6412
female (6246) 6246
otorhinolaryngology (5756) 5756
adult (4096) 4096
middle aged (3620) 3620
hearing loss (3409) 3409
aged (2576) 2576
audiology & speech-language pathology (2540) 2540
hearing impairment (2307) 2307
animals (2212) 2212
child (2115) 2115
deafness (1998) 1998
adolescent (1988) 1988
neurosciences (1875) 1875
hearing (1618) 1618
child, preschool (1476) 1476
hearing loss, sensorineural - diagnosis (1448) 1448
hearing loss, sensorineural - etiology (1441) 1441
children (1417) 1417
hearing loss, sensorineural - physiopathology (1317) 1317
hearing-loss (1306) 1306
otorhinolaryngologic diseases (1293) 1293
young adult (1218) 1218
audiometry, pure-tone (1208) 1208
hearing aids (1176) 1176
magnetic resonance imaging (1157) 1157
mutation (1155) 1155
noise (1147) 1147
sensorineural hearing-loss (1133) 1133
surgery (1014) 1014
abridged index medicus (1010) 1010
audiometry (1008) 1008
retrospective studies (1000) 1000
cochlear implants (996) 996
infant (977) 977
auditory threshold (976) 976
mice (964) 964
research (952) 952
analysis (936) 936
speech perception (912) 912
pediatrics (889) 889
hearing loss, sensorineural - pathology (881) 881
hearing loss, sensorineural - genetics (880) 880
aged, 80 and over (878) 878
ears & hearing (876) 876
cochlea (875) 875
inner-ear (868) 868
treatment outcome (864) 864
article (846) 846
otolaryngology (816) 816
acoustic stimulation (811) 811
diagnosis (799) 799
sensorineural hearing loss (767) 767
genetics & heredity (756) 756
clinical neurology (747) 747
health aspects (699) 699
risk factors (687) 687
cochlea - pathology (655) 655
auditory threshold - physiology (652) 652
speech (649) 649
age (626) 626
care and treatment (626) 626
acoustics (616) 616
cochlear implantation (616) 616
medicine & public health (613) 613
hearing disorders (586) 586
audiology (582) 582
rehabilitation (582) 582
case-control studies (578) 578
tinnitus (568) 568
prevalence (563) 563
disease models, animal (558) 558
time factors (558) 558
medicine, research & experimental (557) 557
sense organs (550) 550
medicine (549) 549
genetic aspects (543) 543
severity of illness index (543) 543
follow-up studies (532) 532
pedigree (529) 529
syndrome (521) 521
tomography, x-ray computed (520) 520
studies (508) 508
impairment (502) 502
phenotype (502) 502
ear (493) 493
evoked potentials, auditory, brain stem (490) 490
infant, newborn (488) 488
adults (485) 485
age factors (480) 480
hearing protection (476) 476
cochlear implant (455) 455
patients (447) 447
prospective studies (443) 443
disease (442) 442
hearing loss - etiology (440) 440
diagnosis, differential (439) 439
cochlea - physiopathology (433) 433
more...
Library Location Library Location
Library Location Library Location
X
Sort by Item Count (A-Z)
Filter by Count
Gerstein Science - Stacks (287) 287
UTL at Downsview - May be requested (38) 38
Robarts - Stacks (35) 35
OISE - Stacks (33) 33
Collection Dvlpm't (Acquisitions) - Vendor file (17) 17
UofT at Mississauga - Stacks (12) 12
Collection Dvlpm't (Acquisitions) - Closed Orders (9) 9
Holland Bloorview Kids Rehabilitation - Stacks (9) 9
Providence Healthcare - Stacks (6) 6
Online Resources - Online (4) 4
Aerospace - Stacks (3) 3
UofT at Scarborough - Stacks (3) 3
Engineering & Comp. Sci. - Stacks (2) 2
Gerstein Science - Not Returned (2) 2
Gerstein Science - Reference (2) 2
Music - Stacks (2) 2
St. Michael's Hospital - Stacks (2) 2
Sunnybrook Health Sciences Centre - Sunnybrook Stacks (2) 2
Baycrest Hospital - Stacks (1) 1
Faculty of Information - Subject Analysis Systems (1) 1
Gerstein Science - Circulation Desk (1) 1
Gerstein Science - Missing (1) 1
Holland Bloorview Kids Rehabilitation - Reference (1) 1
Knox College (Caven) - Stacks (1) 1
Lakeridge Health Sciences - Oshawa (1) 1
OISE - Lost (1) 1
OISE - Reference (1) 1
Scarborough Hospital - General (1) 1
Stacks (1) 1
UofT at Scarborough - Withdrawn (1) 1
West Park Healthcare Centre - Hospital Department (1) 1
West Park Healthcare Centre - Stacks (1) 1
more...
Language Language
Language Language
X
Sort by Item Count (A-Z)
Filter by Count
English (12922) 12922
German (86) 86
Spanish (62) 62
French (53) 53
Russian (43) 43
Japanese (35) 35
Chinese (31) 31
Polish (24) 24
Portuguese (24) 24
Italian (18) 18
Korean (12) 12
Turkish (7) 7
Arabic (4) 4
Croatian (3) 3
Romanian (3) 3
Dutch (2) 2
Finnish (2) 2
Czech (1) 1
Hebrew (1) 1
Hungarian (1) 1
Language (1) 1
Norwegian (1) 1
Sign (1) 1
Swedish (1) 1
Ukrainian (1) 1
more...
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


Neuron, ISSN 0896-6273, 2008, Volume 57, Issue 2, pp. 263 - 275
Journal Article
The American Journal of Human Genetics, ISSN 0002-9297, 09/2016, Volume 99, Issue 3, pp. 770 - 776
Journal Article
American Journal of Medical Genetics Part A, ISSN 1552-4825, 07/2018, Volume 176, Issue 7, pp. 1587 - 1593
Ocular albinism type 1 (OA1) is caused by mutations in the GPR143 gene located at Xp22.2. The manifestations, which are due to hypopigmentation, are confined... 
albinism, ocular albinism, OA1 | GPR143 | contiguous gene deletion syndrome | SHROOM2 | male infertility, oligozoospermia, asthenozoospermia, X chromosome | hearing loss | TBL1X | albinism, ocular albinism, OA1, GPR143, hearing loss, TBL1X, male infertility, oligozoospermia, asthenozoospermia, X chromosome, SHROOM2 | ocular albinism | oligozoospermia | X chromosome | CLINICAL-FEATURES | PREVALENCE | male infertility | albinism | DELETION | GENE | CLONING | GENETICS & HEREDITY | asthenozoospermia | DEAFNESS | MUTATIONS | TYPE-1 | OA1 | Albinism, Ocular - pathology | Infertility - pathology | Humans | Middle Aged | Genetic Diseases, X-Linked - complications | Male | Infertility - genetics | Gene Deletion | Adult | Female | Genetic Diseases, X-Linked - genetics | Eye Proteins - genetics | Albinism, Ocular - genetics | Transducin - genetics | Membrane Proteins - genetics | Hearing Loss, Sensorineural - pathology | Hearing Loss, Sensorineural - genetics | Infertility - complications | Albinism, Ocular - complications | Membrane Glycoproteins - genetics | Pedigree | Genetic Diseases, X-Linked - pathology | Aged | Hearing Loss, Sensorineural - complications | Mutation | Albinism | Infertility | Genes | Hearing loss | Hearing | Clonal deletion | Ocular albinism | Hearing protection | Gene deletion | Hearing impairment | Pigmentation | Index Medicus
Journal Article
Journal Article