X
Search Filters
Format Format
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
humans (279) 279
female (273) 273
pregnancy (250) 250
obstetrics & gynecology (245) 245
adult (230) 230
index medicus (211) 211
prenatal diagnosis (173) 173
gynecology and obstetrics (169) 169
internal medicine (162) 162
obstetrics and gynecology (162) 162
amniocentesis (153) 153
obstetrics and gynaecology (134) 134
male (96) 96
mosaicism (95) 95
genetics & heredity (89) 89
ultrasonography, prenatal (89) 89
comparative genomic hybridization (86) 86
chromosome deletion (68) 68
karyotyping (64) 64
in situ hybridization, fluorescence (53) 53
infant, newborn (53) 53
phenotype (48) 48
trisomy - diagnosis (48) 48
abnormalities, multiple - genetics (45) 45
fetal diseases - genetics (36) 36
karyotype (33) 33
prenatal diagnosis - methods (33) 33
prenatal-diagnosis (32) 32
mutations (31) 31
polymerase chain reaction (30) 30
chromosome aberrations (28) 28
trisomy (28) 28
trisomy - genetics (28) 28
fetal diseases - diagnosis (27) 27
fetus (27) 27
ultrasound (27) 27
gene (26) 26
deletion (25) 25
diagnosis (25) 25
pregnancy trimester, second (25) 25
genetic markers (23) 23
gestational age (23) 23
mutation (23) 23
abortion, eugenic (22) 22
abortion, induced (22) 22
ultrasonography (22) 22
cytogenetic analysis (21) 21
diagnosis, differential (21) 21
infant (20) 20
patient (20) 20
pregnant women (20) 20
translocation, genetic (20) 20
abnormalities, multiple - diagnosis (19) 19
duplication (19) 19
fish (19) 19
translocation (18) 18
abnormalities, multiple - diagnostic imaging (17) 17
amniocentesis - methods (17) 17
aneuploidy (17) 17
cytogenetics (17) 17
intellectual disability - genetics (16) 16
maternal age (16) 16
chromosome disorders - diagnosis (15) 15
chromosome disorders - genetics (15) 15
chromosomes, human, pair 18 (15) 15
abnormal karyotype (14) 14
child (14) 14
fetal diseases - diagnostic imaging (14) 14
fetal growth retardation - genetics (14) 14
genetic testing (14) 14
origin (14) 14
research (14) 14
abnormalities (13) 13
amnion - cytology (13) 13
expression (13) 13
genetic aspects (13) 13
fetal growth retardation - diagnostic imaging (12) 12
pregnancy outcome (12) 12
chromosome duplication (11) 11
comparative genomic hybridization - methods (11) 11
holoprosencephaly - genetics (11) 11
identification (11) 11
in situ hybridization, fluorescence - methods (11) 11
small supernumerary marker chromosome (11) 11
uncultured amniocytes (11) 11
uniparental disomy - diagnosis (11) 11
adolescent (10) 10
cells, cultured (10) 10
chromosomes, human, pair 18 - genetics (10) 10
chromosomes, human, pair 2 (10) 10
congenital, hereditary, and neonatal diseases and abnormalities (10) 10
dna - analysis (10) 10
genes (10) 10
holoprosencephaly (10) 10
in-situ hybridization (10) 10
medical colleges (10) 10
mental-retardation (10) 10
pregnancy trimester, first (10) 10
region (10) 10
reproductive biology (10) 10
more...
Language Language
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


Taiwanese Journal of Obstetrics & Gynecology, ISSN 1028-4559, 11/2019, Volume 58, Issue 6, pp. 855 - 858
We present prenatal diagnosis of mosaic isochromosome 20q [i(20q)] at amniocentesis, and we review the literature. A 36-year-old woman underwent amniocentesis... 
Amniocentesis | Isochromosome 20q | Mosaicism | Amniocytes | Prenatal diagnosis
Journal Article
Taiwanese Journal of Obstetrics & Gynecology, ISSN 1028-4559, 11/2019, Volume 58, Issue 6, pp. 852 - 854
We present prenatal diagnosis of mosaicism for trisomy 7 in a single colony at amniocentesis with a favorable outcome. A 40-year-old woman underwent... 
Amniocentesis | Mosaicism | Prenatal diagnosis | Single colony | Trisomy 7
Journal Article
Taiwanese Journal of Obstetrics & Gynecology, ISSN 1028-4559, 11/2019, Volume 58, Issue 6, pp. 869 - 871
We present a familial 21q22.3 microduplication in a fetus associated with prenatally detected congenital heart defects (CHD). A 38-year-old woman underwent... 
Congenital heart defects | Prenatal diagnosis | 21q22.3 microduplication
Journal Article
Journal Article
Gene, ISSN 0378-1119, 12/2013, Volume 532, Issue 1, pp. 152 - 159
Journal Article
Taiwanese Journal of Obstetrics & Gynecology, ISSN 1028-4559, 11/2019, Volume 58, Issue 6, pp. 864 - 868
We present prenatal diagnosis and molecular cytogenetic characterization of a small supernumerary marker chromosome (sSMC) derived from chromosome 3. A... 
Small supernumerary marker chromosome | FISH | Prenatal diagnosis | Chromosome 3 | aCGH
Journal Article
Taiwanese Journal of Obstetrics & Gynecology, ISSN 1028-4559, 11/2019, Volume 58, Issue 6, pp. 859 - 863
We present detection of a familial 1q21.1 microdeletion and concomitant mutation in a fetus with oligohydramnios and bilateral renal dysplasia on prenatal... 
Missense mutation | CHD1L | Oligohydramnios | Bilateral renal dysplasia | 1q21.1 microdeletion
Journal Article
Ultrasound in Medicine & Biology, ISSN 0301-5629, 2009, Volume 35, Issue 8, pp. S196 - S196
Journal Article
Taiwanese journal of obstetrics & gynecology, 08/2018, Volume 57, Issue 4, p. 578
We present prenatal diagnosis of a 2p16.1-p15 duplication associated with familial intellectual disability, and we discuss the genotype-phenotype correlation.... 
Amniocentesis | Humans | Male | Chromosome Duplication - genetics | Amnion - chemistry | Gestational Age | DNA - blood | Intellectual Disability - genetics | Pregnancy | Phenotype | Comparative Genomic Hybridization | DNA - analysis | Pedigree | Ultrasonography, Prenatal | Karyotyping | Adult | Female | Infant, Newborn
Journal Article
Journal Article
Journal Article
No results were found for your search.

Cannot display more than 1000 results, please narrow the terms of your search.