X
Search Filters
Format Format
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
humans (21) 21
genetics & heredity (17) 17
index medicus (14) 14
female (13) 13
male (12) 12
adult (10) 10
phenotype (8) 8
adolescent (7) 7
child (7) 7
infant (7) 7
syndrome (7) 7
child, preschool (6) 6
chromosome deletion (6) 6
genetics (6) 6
abnormalities (5) 5
abnormalities, multiple - genetics (5) 5
article (5) 5
chromosome aberrations (5) 5
diagnosis (5) 5
genetic aspects (5) 5
in situ hybridization, fluorescence (5) 5
middle aged (5) 5
mutation (5) 5
mutations (5) 5
young adult (5) 5
cardiomyopathy (4) 4
human genetics (4) 4
microdeletion (4) 4
molecular medicine (4) 4
obstetrics & gynecology (4) 4
patient (4) 4
pregnancy (4) 4
abortion, spontaneous - genetics (3) 3
analysis (3) 3
barth syndrome (3) 3
biomedicine (3) 3
cardiolipin (3) 3
chromosomes, human, pair 22 - genetics (3) 3
comparative genomic hybridization (3) 3
congenital (3) 3
cytogenetic analysis (3) 3
echocardiography (3) 3
gene (3) 3
gene deletion (3) 3
genes (3) 3
genetic research (3) 3
heart (3) 3
internal medicine (3) 3
medical colleges (3) 3
medical genetics (3) 3
miscarriage (3) 3
reproductive biology (3) 3
research (3) 3
spontaneous-abortions (3) 3
velocardiofacial syndrome (3) 3
abortion, spontaneous - diagnosis (2) 2
aged (2) 2
aneuploidy (2) 2
anomalies (2) 2
barth syndrome - diagnosis (2) 2
barth syndrome - metabolism (2) 2
brain (2) 2
cardio-facial syndrome (2) 2
children (2) 2
chromosome 22 (2) 2
chromosome mapping (2) 2
chromosomes (2) 2
clinical neurology (2) 2
cohort studies (2) 2
conception (2) 2
cross-sectional studies (2) 2
cytogenetics (2) 2
defects (2) 2
disease (2) 2
dll3 (2) 2
dna microarrays (2) 2
exercise (2) 2
expression (2) 2
gene mutations (2) 2
genetic (2) 2
genomics (2) 2
genotype (2) 2
genotype & phenotype (2) 2
health aspects (2) 2
infant, newborn (2) 2
intellectual disability - genetics (2) 2
intracellular signaling peptides and proteins (2) 2
karyotype (2) 2
kyphosis (2) 2
linked cardioskeletal myopathy (2) 2
management (2) 2
membrane proteins - genetics (2) 2
metabolic diseases (2) 2
metabolism (2) 2
mitochondria (2) 2
neoplasms (2) 2
neurological disorders (2) 2
neurosciences (2) 2
neutropenia (2) 2
nuclear receptor set-domain-containing protein (2) 2
more...
Language Language
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


Obstetrics & Gynecology, ISSN 0029-7844, 05/2019, Volume 133 Suppl 1, pp. 164 - 165
INTRODUCTION:To evaluate the origin of the retained X chromosome using SNP microarray in patients with monosomy X presenting with pregnancy loss. Monosomy X is... 
Journal Article
Fertility and Sterility, ISSN 0015-0282, 09/2019, Volume 112, Issue 3, pp. e120 - e120
Journal Article
Journal Article
Obstetrics & Gynecology, ISSN 0029-7844, 05/2018, Volume 131 Suppl 1, pp. 117S - 117S
INTRODUCTION:Noninvasive prenatal screening (NIPT) is a sensitive screen focusing on common aneuploidies. Products of conception (POC) testing can detect all... 
Journal Article
neurogenetics, ISSN 1364-6745, 2/2013, Volume 14, Issue 1, pp. 11 - 22
Journal Article
Human mutation, ISSN 1059-7794, 2010, Volume 31, Issue 10, pp. 1142 - 1154
Journal Article
The American Journal of Human Genetics, ISSN 0002-9297, 06/2009, Volume 84, Issue 6, pp. 780 - 791
Journal Article
Journal of Inherited Metabolic Disease, ISSN 0141-8955, 1/2013, Volume 36, Issue 1, pp. 91 - 101
Journal Article
Journal of Medical Genetics, ISSN 0022-2593, 02/2007, Volume 44, Issue 2, pp. 89 - 98
Journal Article
American Journal of Physiology - Heart and Circulatory Physiology, ISSN 0363-6135, 11/2011, Volume 301, Issue 5, pp. H2122 - H2129
Spencer CT, Byrne BJ, Bryant RM, Margossian R, Maisenbacher M, Breitenger P, Benni PB, Redfearn S, Marcus E, Cade WT. Impaired cardiac reserve and severely... 
Mitochondria | Cardiolipin | Congenital | Cardiomyopathy | CARDIAC & CARDIOVASCULAR SYSTEMS | PHYSIOLOGY | mitochondria | OXYGENATION | HEART-FAILURE | congenital | cardiolipin | L-CARNITINE | DISEASE | NEAR-INFRARED SPECTROSCOPY | PERIPHERAL VASCULAR DISEASE | cardiomyopathy | AGE-ASSOCIATED DECLINE | MITOCHONDRIAL MYOPATHIES | NEWBORN-INFANTS | BLOOD
Journal Article