X
Search Filters
Format Format
Format Format
X
Sort by Item Count (A-Z)
Filter by Count
Journal Article (537) 537
Publication (87) 87
Book Chapter (6) 6
Conference Proceeding (5) 5
Book / eBook (3) 3
Dissertation (1) 1
Magazine Article (1) 1
more...
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
humans (267) 267
genetics & heredity (221) 221
index medicus (185) 185
female (155) 155
male (127) 127
phenotype (78) 78
in situ hybridization, fluorescence (77) 77
chromosome deletion (66) 66
adult (61) 61
abnormalities, multiple - genetics (58) 58
biochemistry & molecular biology (58) 58
comparative genomic hybridization (56) 56
child (55) 55
research (54) 54
genetics (52) 52
intellectual disability - genetics (50) 50
analysis (48) 48
chromosome aberrations (47) 47
karyotyping (46) 46
animals (44) 44
adolescent (42) 42
array cgh (40) 40
infant (40) 40
pregnancy (40) 40
chromosomes (39) 39
syndrome (39) 39
genomics (38) 38
mental-retardation (38) 38
genetic aspects (37) 37
mosaicism (37) 37
mutation (36) 36
deletion (35) 35
gene (35) 35
obstetrics & gynecology (34) 34
article (33) 33
child, preschool (33) 33
infant, newborn (32) 32
mutations (32) 32
genomes (30) 30
array-cgh (29) 29
biotechnology & applied microbiology (29) 29
cell biology (26) 26
gene duplication (26) 26
aneuploidy (25) 25
diagnosis (25) 25
dna (25) 25
genes (25) 25
base sequence (24) 24
gene deletion (24) 24
middle aged (24) 24
molecular sequence data (24) 24
geosciences, multidisciplinary (23) 23
mental retardation (23) 23
translocation, genetic (23) 23
chromosome mapping (22) 22
copy number (22) 22
dna copy number variations (22) 22
cytogenetics (21) 21
genetic disorders (21) 21
genotype (21) 21
oligonucleotide array sequence analysis (21) 21
rearrangements (21) 21
translocation (20) 20
chromosome disorders - genetics (19) 19
genome, human (19) 19
geochemistry & geophysics (19) 19
hybridization (19) 19
provenance (19) 19
sequence analysis, dna (19) 19
copy number variation (18) 18
further section (18) 18
geochronology (18) 18
microdeletion (18) 18
chromosome banding (17) 17
fish (17) 17
medicine, research & experimental (17) 17
reproductive biology (17) 17
abnormalities (16) 16
duplication (16) 16
expression (16) 16
identification (16) 16
medical education (16) 16
mice (16) 16
nucleic acid hybridization (16) 16
deletions (15) 15
disease (15) 15
human genome (15) 15
medical ethics (15) 15
oligonucleotide array sequence analysis - methods (15) 15
pedigree (15) 15
usage (15) 15
young adult (15) 15
amplification (14) 14
deoxyribonucleic acid--dna (14) 14
gene expression (14) 14
patient (14) 14
polymorphism, single nucleotide (14) 14
prenatal diagnosis (14) 14
prenatal diagnosis - methods (14) 14
software (14) 14
more...
Library Location Library Location
Language Language
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


Annals of oncology, ISSN 0923-7534, 2019, Volume 30, Issue 1, pp. 85 - 95
Background: Early cancer diagnosis might improve survival rates. As circulating tumor DNA (ctDNA) carries cancer-specific modifications, it has great potential... 
DIAGNOSTIC-VALUE | circulating plasma DNA | early cancer detection | ONCOLOGY | liquid biopsies | NONINVASIVE DETECTION | DETECTABLE CLONAL MOSAICISM | copy number alterations
Journal Article
Journal Article
The American Journal of Human Genetics, ISSN 0002-9297, 05/2010, Volume 86, Issue 5, pp. 749 - 764
Journal Article
by Mefford, Heather C and Sharp, Anew J and Baker, Carl and Itsara, Andy and Jiang, Zhaoshi and Buysse, Karen and Huang, Shuwen and Maloney, Viv K and Crolla, John A and Baralle, Diana and Collins, Amanda and Mercer, Catherine and Norga, Koen and de Ravel, Thomy and Devriendt, Koen and Bongers, Ernie M. H. F and de Leeuw, Nicole and Reardon, William and Gimelli, Stefania and Bena, Frederique and Hennekam, Raoul C and Male, Alison and Gaunt, Lorraine and Clayton-Smith, Jill and Simonic, Ingrid and Park, Soo Mi and Mehta, Sarju G and Nik-Zainal, Serena and Woods, C. Geoffrey and Firth, Helen V and Parkin, Georgina and Fichera, Marco and Reitano, Santina and Lo Giudice, Mariangela and Li, Kelly E and Casuga, Iris and Broomer, Adam and Conrad, Bernard and Schwerzmann, Markus and Raber, Lorenz and Gallati, Sabina and Striano, Pasquale and Coppola, Antonietta and Tolmie, John L and Tobias, Edward S and Lilley, Chris and Armengol, Lluis and Spysschaert, Yves and Verloo, Patrick and de Coene, Anja and Goossens, Linde and Mortier, Geert and Speleman, Frank and van Binsbergen, Ellen and Nelen, Marcel R and Hochstenbach, Ron and Poot, Martin and Gallagher, Louise and Gill, Michael and McClellan, Jon and King, Mary-Claire and Regan, Regina and Skinner, Cindy and Stevenson, Roger E and Antonarakis, Stylianos E and Chen, Caifu and Estivill, Xavier and Menten, Bjorn and Gimelli, Giorgio and Gribble, Susan and Schwartz, Stuart and Sutcliffe, James S and Walsh, Tom and Knight, Samantha J. L and Sebat, Jonathan and Romano, Corrado and Schwartz, Charles E and Veltman, Joris A and de Vries, Bert B. A and Vermeesch, Joris R and Barber, John C. K and Willatt, Lionel and Tassabehji, May and Eichler, Evan E
New England journal of medicine, ISSN 0028-4793, 2008, Volume 359, Issue 16, pp. 1685 - U130
Journal Article
Journal of Medical Genetics, ISSN 0022-2593, 08/2009, Volume 46, Issue 8, pp. 511 - 523
Journal Article
Journal Article