X
Search Filters
Format Format
Format Format
X
Sort by Item Count (A-Z)
Filter by Count
Journal Article (615) 615
Book Review (145) 145
Publication (72) 72
Book Chapter (12) 12
Dissertation (3) 3
Conference Proceeding (2) 2
Web Resource (2) 2
Streaming Video (1) 1
more...
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
index medicus (508) 508
humans (492) 492
female (309) 309
genetics & heredity (290) 290
silver-russell-syndrome (282) 282
male (272) 272
genomic imprinting (248) 248
silver-russell syndrome (234) 234
dna methylation (201) 201
silver-russell syndrome - genetics (171) 171
methylation (147) 147
phenotype (145) 145
uniparental disomy (136) 136
beckwith-wiedemann-syndrome (131) 131
child (120) 120
beckwith-wiedemann syndrome (103) 103
mutation (100) 100
adult (99) 99
child, preschool (95) 95
pregnancy (95) 95
imprinting (92) 92
growth (91) 91
syndrome (88) 88
animals (86) 86
infant, newborn (86) 86
biochemistry & molecular biology (85) 85
infant (79) 79
beckwith-wiedemann syndrome - genetics (74) 74
endocrinology & metabolism (71) 71
gene (67) 67
adolescent (66) 66
genetics (66) 66
epigenetics (65) 65
pediatrics (65) 65
silver-russell syndrome - diagnosis (65) 65
growth disorders - genetics (64) 64
abnormalities, multiple - genetics (62) 62
genes (62) 62
research (62) 62
genetic aspects (60) 60
region (60) 60
silver–russell syndrome (60) 60
chromosomes, human, pair 11 - genetics (59) 59
fetal growth retardation - genetics (59) 59
insulin-like growth factor ii - genetics (58) 58
epigenesis, genetic (57) 57
genomic imprinting - genetics (57) 57
russell-silver syndrome (57) 57
analysis (54) 54
hypomethylation (54) 54
mice (54) 54
chromosome 11p15 (53) 53
gene expression (53) 53
expression (52) 52
prader-willi-syndrome (52) 52
maternal uniparental disomy (51) 51
growth-retardation (50) 50
mosaicism (49) 49
alleles (47) 47
chromosomes, human, pair 7 - genetics (46) 46
imprinting center region (46) 46
proteins - genetics (46) 46
uniparental disomy - genetics (44) 44
h19 (43) 43
genomics (42) 42
mutations (42) 42
chromosomes, human, pair 7 (41) 41
chromosomes, human, pair 11 (40) 40
genetic disorders (40) 40
pedigree (40) 40
11p15 (38) 38
children (37) 37
rna, long noncoding (36) 36
short stature (36) 36
chromosome 7 (35) 35
chromosomes (35) 35
dna methylation - genetics (35) 35
in-vitro fertilization (35) 35
obstetrics & gynecology (35) 35
diagnosis (34) 34
genetic research (34) 34
cell biology (31) 31
chromosome aberrations (31) 31
dna (31) 31
igf2 (31) 31
rna, long noncoding - genetics (31) 31
rna, untranslated - genetics (31) 31
deletion (30) 30
including grb10 (30) 30
isodisomy (30) 30
base sequence (28) 28
chromosome-7 (28) 28
duplication (28) 28
for-gestational-age (28) 28
genetic testing (28) 28
human genetics (28) 28
karyotyping (28) 28
life sciences (28) 28
reproductive biology (28) 28
sequence analysis, dna (28) 28
more...
Library Location Library Location
Language Language
Language Language
X
Sort by Item Count (A-Z)
Filter by Count
English (599) 599
German (10) 10
Polish (7) 7
Chinese (5) 5
French (3) 3
Spanish (3) 3
Japanese (2) 2
Portuguese (1) 1
more...
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


European journal of human genetics, ISSN 1018-4813, 2016, Volume 24, Issue 10, pp. 1377 - 1387
Journal Article
Human Molecular Genetics, ISSN 0964-6906, 1/2012, Volume 21, Issue 1, pp. 10 - 25
Journal Article
Journal Article
Human Mutation, ISSN 1059-7794, 04/2013, Volume 34, Issue 4, pp. 595 - 602
Journal Article
Journal Article
Journal Article
Human Reproduction, ISSN 0268-1161, 8/2012, Volume 27, Issue 8, pp. 2541 - 2548
Journal Article
Journal Article