UofT Libraries is getting a new library services platform in January 2021.
Learn more about the change.

Search Articles

X
Search Filters
Format Format
Format Format
X
Sort by Item Count (A-Z)
Filter by Count
Journal Article (6297) 6297
Book Chapter (79) 79
Book / eBook (12) 12
Magazine Article (8) 8
Reference (5) 5
Dissertation (4) 4
Conference Proceeding (2) 2
Newsletter (2) 2
Newspaper Article (2) 2
more...
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
humans (5153) 5153
science & technology (4479) 4479
life sciences & biomedicine (4301) 4301
female (4077) 4077
trisomy (3553) 3553
pregnancy (2361) 2361
male (2150) 2150
biological and medical sciences (1991) 1991
medical sciences (1940) 1940
adult (1933) 1933
genetics & heredity (1898) 1898
chromosome aberrations (1512) 1512
obstetrics & gynecology (1299) 1299
down syndrome (1210) 1210
trisomy 21 (1174) 1174
karyotyping (1163) 1163
medical genetics (1162) 1162
prenatal diagnosis (1058) 1058
infant, newborn (1055) 1055
trisomy - genetics (938) 938
chromosomes, human, pair 18 (921) 921
aneuploidy (806) 806
trisomy - diagnosis (764) 764
gynecology. andrology. obstetrics (758) 758
down syndrome - genetics (747) 747
down syndrome - diagnosis (744) 744
infant (733) 733
chromosomes (658) 658
abnormalities, multiple - genetics (643) 643
mosaicism (632) 632
middle aged (616) 616
adolescent (610) 610
child (606) 606
in situ hybridization, fluorescence (598) 598
child, preschool (585) 585
trisomy 18 (524) 524
phenotype (515) 515
prenatal diagnosis - methods (494) 494
ultrasonography, prenatal (491) 491
gestational age (487) 487
maternal age (462) 462
pediatrics (460) 460
analysis (454) 454
pregnancy. fetus. placenta (453) 453
translocation, genetic (443) 443
chromosomes, human, pair 13 (432) 432
retrospective studies (432) 432
fetuses (431) 431
chromosome disorders (430) 430
amniocentesis (424) 424
abridged index medicus (400) 400
animals (391) 391
down's syndrome (386) 386
pregnant women (384) 384
management. prenatal diagnosis (379) 379
syndrome (373) 373
risk factors (365) 365
pregnancy trimester, first (332) 332
young adult (317) 317
radiology, nuclear medicine & medical imaging (306) 306
trisomy 18 syndrome (306) 306
chromosomes, human, pair 18 - genetics (305) 305
mice (300) 300
oncology (299) 299
genetics (298) 298
technology (297) 297
hematology (294) 294
chromosome deletion (293) 293
cytogenetics (291) 291
research (290) 290
acoustics (280) 280
chromosome banding (277) 277
chromosome disorders - diagnosis (264) 264
trisomy 13 (262) 262
diagnosis (259) 259
deoxyribonucleic acid--dna (258) 258
aged (256) 256
neurosciences & neurology (254) 254
intellectual disability - genetics (253) 253
down syndrome - diagnostic imaging (251) 251
pregnancy trimester, second (242) 242
sensitivity and specificity (241) 241
chromosomes, human, 16-18 (240) 240
ultrasound (240) 240
trisomy 13 syndrome (237) 237
down syndrome - pathology (236) 236
research article (235) 235
fundamental and applied biological sciences. psychology (234) 234
age (227) 227
genetic aspects (226) 226
medicine (220) 220
hematologic and hematopoietic diseases (217) 217
down syndrome - complications (216) 216
genes (216) 216
chromosome disorders - genetics (209) 209
pedigree (209) 209
fetus (207) 207
genetic counseling (207) 207
neurosciences (206) 206
leukemias. malignant lymphomas. malignant reticulosis. myelofibrosis (201) 201
more...
Library Location Library Location
Language Language
Language Language
X
Sort by Item Count (A-Z)
Filter by Count
English (6180) 6180
German (71) 71
French (59) 59
Spanish (39) 39
Chinese (35) 35
Japanese (34) 34
Portuguese (26) 26
Polish (19) 19
Italian (13) 13
Russian (11) 11
Korean (10) 10
Hungarian (9) 9
Bulgarian (5) 5
Czech (5) 5
Hebrew (4) 4
Romanian (4) 4
Persian (2) 2
Turkish (2) 2
Dutch (1) 1
Norwegian (1) 1
Serbian (1) 1
Slovak (1) 1
Slovenian (1) 1
Welsh (1) 1
more...
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


American journal of obstetrics and gynecology, ISSN 0002-9378, 12/2017, Volume 217, Issue 6, pp. 691.e1 - 691.e6
amniocentesis | trisomy 13 | trisomy 21 | 47,XXY | noninvasive prenatal testing | noninvasive prenatal screening | 47,XXX | 47,XYY | cell-free DNA | NIPT | prenatal diagnosis | microdeletion syndrome | trisomy 18 | Life Sciences & Biomedicine | Obstetrics & Gynecology | Science & Technology | Chromosome Disorders - blood | Predictive Value of Tests | Turner Syndrome - blood | Cri-du-Chat Syndrome - diagnosis | Humans | Angelman Syndrome - diagnosis | Sex Chromosome Disorders of Sex Development - genetics | Turner Syndrome - diagnosis | Sex Chromosome Disorders of Sex Development - blood | Trisomy 18 Syndrome - diagnosis | Cri-du-Chat Syndrome - genetics | Klinefelter Syndrome - blood | Klinefelter Syndrome - genetics | Sex Chromosome Aberrations | Microarray Analysis | Karyotyping | Down Syndrome - blood | Angelman Syndrome - genetics | Chorionic Villi Sampling | Chromosome Disorders - diagnosis | Prader-Willi Syndrome - genetics | Female | Down Syndrome - diagnosis | Amniocentesis | Prader-Willi Syndrome - diagnosis | Trisomy 13 Syndrome - genetics | Chromosomes, Human, X - genetics | Prader-Willi Syndrome - blood | Prenatal Diagnosis | In Situ Hybridization, Fluorescence | Cri-du-Chat Syndrome - blood | Pregnancy | Trisomy 18 Syndrome - blood | Sex Chromosome Disorders of Sex Development - diagnosis | Trisomy - diagnosis | Trisomy - genetics | Trisomy 13 Syndrome - blood | Cell-Free Nucleic Acids - blood | Trisomy 18 Syndrome - genetics | Down Syndrome - genetics | Klinefelter Syndrome - diagnosis | Turner Syndrome - genetics | Angelman Syndrome - blood | Trisomy 13 Syndrome - diagnosis | Chromosome Disorders - genetics | DNA microarrays | Medical screening | Pregnant women | Chromosomes | Analysis | Index Medicus | Abridged Index Medicus
Journal Article
Journal Article
Ultrasound in obstetrics & gynecology, ISSN 0960-7692, 03/2009, Volume 33, Issue 3, pp. 259 - 264
Journal Article
Ultrasound in obstetrics & gynecology, ISSN 0960-7692, 05/2009, Volume 33, Issue 5, pp. 512 - 517
Journal Article