X
Search Filters
Format Format
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
index medicus (16) 16
humans (15) 15
male (11) 11
female (10) 10
genetics & heredity (9) 9
child (8) 8
genetic aspects (7) 7
mutation (7) 7
child, preschool (6) 6
genetics (6) 6
adult (5) 5
genes (5) 5
research (5) 5
animals (4) 4
base sequence (4) 4
endocrinology & metabolism (4) 4
intellectual disability - genetics (4) 4
polymorphism, single nucleotide (4) 4
short stature (4) 4
adolescent (3) 3
amino acid sequence (3) 3
cell biology (3) 3
chromosome deletion (3) 3
clonal deletion (3) 3
deletion (3) 3
dwarfism - genetics (3) 3
expression (3) 3
gene (3) 3
genomes (3) 3
growth (3) 3
infant (3) 3
infant, newborn (3) 3
insulin-like growth factor i - genetics (3) 3
molecular sequence data (3) 3
pediatrics (3) 3
pedigree (3) 3
phenotype (3) 3
physiological aspects (3) 3
young adult (3) 3
abnormalities, multiple (2) 2
abnormalities, multiple - genetics (2) 2
acid-labile subunit (2) 2
article (2) 2
binding (2) 2
biochemistry & molecular biology (2) 2
body height - genetics (2) 2
carrier proteins - genetics (2) 2
chromosomes, human, pair 16 (2) 2
comparative genomic hybridization (2) 2
diagnosis (2) 2
dna copy number variations (2) 2
dna mutational analysis (2) 2
factor-i (2) 2
factor-i receptor (2) 2
further section (2) 2
gene deletion (2) 2
gene duplication (2) 2
gene mutations (2) 2
genetic association studies (2) 2
genome, human - genetics (2) 2
genome-wide association (2) 2
genotype & phenotype (2) 2
growth disorders (2) 2
growth disorders - genetics (2) 2
growth-retardation (2) 2
heterozygous expression (2) 2
human height (2) 2
idiopathic short stature (2) 2
igf1 (2) 2
insulin-like growth factor i - metabolism (2) 2
mice (2) 2
microcephaly (2) 2
microdeletion (2) 2
microdeletion syndrome (2) 2
middle aged (2) 2
missense mutation (2) 2
original paper (2) 2
rats (2) 2
risk factors (2) 2
sequence deletion (2) 2
small for gestational age (2) 2
1506 (1) 1
22q11.2 (1) 1
5' untranslated regions - genetics (1) 1
abnormalities, multiple - pathology (1) 1
abridged index medicus (1) 1
abstracts (1) 1
adaptor proteins, signal transducing - genetics (1) 1
adenoma - genetics (1) 1
adenoma - pathology (1) 1
adenoma resistance locus (1) 1
advanced basic science (1) 1
aged (1) 1
alleles (1) 1
apoptosis (1) 1
arpkd (1) 1
array-cgh (1) 1
arrays (1) 1
associative learning (1) 1
autism (1) 1
more...
Language Language
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


Nature Genetics, ISSN 1061-4036, 2012, Volume 44, Issue 4, pp. 435 - 439, S1-2
Journal Article
Hormone Research in Paediatrics, ISSN 1663-2818, 05/2012, Volume 77, Issue 4, pp. 250 - 260
Journal Article
Journal Article
European Journal of Human Genetics, ISSN 1018-4813, 2014, Volume 22, Issue 5, pp. 602 - 609
Journal Article
The Journal of Clinical Endocrinology & Metabolism, ISSN 0021-972X, 11/2010, Volume 95, Issue 11, pp. E363 - E367
Journal Article
European Journal of Human Genetics, ISSN 1018-4813, 2016, Volume 24, Issue 8, pp. 1145 - 1153
Journal Article
Nature Genetics, ISSN 1061-4036, 2012, Volume 44, pp. 1375 - 1381
Congenital central hypothyroidism occurs either in isolation or in conjunction with other pituitary hormone deficits. Using exome and candidate gene... 
Journal Article
PLoS ONE, ISSN 1932-6203, 2011, Volume 6, Issue 2, p. e14727
Journal Article
European journal of human genetics, ISSN 1018-4813, 2014, Volume 22, Issue 5, pp. 602 - 609
Height is a highly heritable and classic polygenic trait. Recent genome-wide association studies (GWAS) have revealed that at least 180 genetic variants... 
Journal Article