X
Search Filters
Format Format
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
humans (9) 9
adult (7) 7
female (5) 5
gene (5) 5
index medicus (5) 5
male (5) 5
adolescent (4) 4
biochemistry & molecular biology (3) 3
genetics & heredity (3) 3
pedigree (3) 3
activating transcription factor 6 - genetics (2) 2
activating transcription factor 6 - metabolism (2) 2
aged (2) 2
animals (2) 2
article (2) 2
base sequence (2) 2
cell differentiation (2) 2
cell membrane - metabolism (2) 2
cell membrane - pathology (2) 2
child, preschool (2) 2
collagen type i - deficiency (2) 2
collagen type i - genetics (2) 2
congenital, hereditary, and neonatal diseases and abnormalities (2) 2
cyclic amp response element-binding protein - genetics (2) 2
cyclic amp response element-binding protein - metabolism (2) 2
dna mutational analysis (2) 2
expression (2) 2
frequency (2) 2
gene expression regulation (2) 2
genes, recessive (2) 2
genetics (2) 2
hydroxylation (2) 2
infant (2) 2
infant, newborn (2) 2
metalloendopeptidases - genetics (2) 2
metalloendopeptidases - metabolism (2) 2
middle aged (2) 2
mutation (2) 2
mutation, missense (2) 2
nerve tissue proteins - genetics (2) 2
nerve tissue proteins - metabolism (2) 2
osteoblasts - metabolism (2) 2
osteoblasts - pathology (2) 2
osteogenesis imperfecta - genetics (2) 2
osteogenesis imperfecta - metabolism (2) 2
osteogenesis imperfecta - pathology (2) 2
procollagen-lysine, 2-oxoglutarate 5-dioxygenase - genetics (2) 2
procollagen-lysine, 2-oxoglutarate 5-dioxygenase - metabolism (2) 2
proteolysis (2) 2
research (2) 2
research article (2) 2
severity of illness index (2) 2
short report (2) 2
sterol regulatory element binding proteins - genetics (2) 2
sterol regulatory element binding proteins - metabolism (2) 2
syndrome (2) 2
thailand (2) 2
3rd locus (1) 1
610 medicine & health (1) 1
8q23.3-q24.1 (1) 1
adcme (1) 1
adenocarcinoma (1) 1
age (1) 1
alleles (1) 1
amastia (1) 1
amastia athelia (1) 1
amino acid sequence (1) 1
amino acid substitution - genetics (1) 1
arpkd (1) 1
asian continental ancestry group (1) 1
athelia (1) 1
autosomal recessive polycystic kidney disease (1) 1
bafme (1) 1
balanced chromosome translocation (1) 1
benign (1) 1
benign adult familial myoclonic epilepsy (1) 1
bone-formation (1) 1
breast (1) 1
breast - abnormalities (1) 1
breast - growth & development (1) 1
cancer (1) 1
cancer-risk (1) 1
carcinoma (1) 1
carrier proteins - genetics (1) 1
case report (1) 1
cercopithecus aethiops (1) 1
child (1) 1
chondrodysplasia punctata - genetics (1) 1
chondrodysplasia punctata type 2 (1) 1
chromosome 3 (1) 1
chromosome 8 (1) 1
chromosome mapping (1) 1
chromosomes (1) 1
chromosomes, human, pair 3 - genetics (1) 1
cleavage (1) 1
collagen (1) 1
comparative analysis (1) 1
congenital abnormalities - genetics (1) 1
congenital hepatic fibrosis (1) 1
conradi-hunermann-happle (1) 1
more...
Language Language
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


Journal Article
Thyroid Research, ISSN 1756-6614, 08/2015, Volume 8, Issue 1, p. 11
Circulating thyrotropin receptor messenger ribonucleic acid (TSHR mRNA) assay has been validated in the follow-up of differentiated thyroid carcinoma (DTC)... 
DTC | qPCR | Thyroid mRNA | TSHR mRNA | Medical research | Messenger RNA | Carcinoma | Thyroid diseases | Medicine, Experimental | Thyrotropin | Metastasis | Research | Comparative analysis | Cancer
Journal Article
The Cleft Palate-Craniofacial Journal, ISSN 1055-6656, 3/2006, Volume 43, Issue 2, pp. 152 - 154
Craniofrontonasal syndrome (CFNS) is an X-linked disorder whose main clinical manifestations include coronal craniosynostosis and frontonasal dysplasia. Very... 
EFNB1 | Ephrin-B1 | Mutation analysis | Craniofrontonasal syndrome | SURGERY | EPH RECEPTORS | craniofrontonasal syndrome | mutation analysis | DENTISTRY, ORAL SURGERY & MEDICINE | EPHRINS | ephrin-B1 | Carrier Proteins - genetics | Point Mutation - genetics | Nose - abnormalities | Craniosynostoses - genetics | Humans | Adult | Female | Genetic Diseases, X-Linked - genetics | Syndrome
Journal Article
Molecular Genetics and Metabolism, ISSN 1096-7192, 2010, Volume 99, Issue 2, pp. 160 - 173
Journal Article
World Journal of Gastroenterology, ISSN 1007-9327, 2009, Volume 15, Issue 42, p. 5364
Journal Article
European Journal of Dermatology, ISSN 1167-1122, 2008, Volume 18, Issue 4, pp. 391 - 393
Journal Article
Nature communications, 07/2016, Volume 7, p. 11920
Journal Article
The Cleft Palate-Craniofacial Journal, ISSN 1055-6656, 2005
Journal Article
No results were found for your search.

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