X
Search Filters
Format Format
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
cyclic nucleotide-gated cation channels (6) 6
index medicus (6) 6
color vision defects - genetics (5) 5
genetics & heredity (5) 5
humans (5) 5
ion channels - genetics (5) 5
locus (5) 5
mutation (5) 5
achm3 (4) 4
alpha-subunit (4) 4
animals (4) 4
biochemistry & molecular biology (4) 4
female (4) 4
male (4) 4
pedigree (4) 4
total colourblindness (4) 4
achromatopsia (3) 3
dna mutational analysis (3) 3
gene (3) 3
gene deletion (3) 3
genes (3) 3
gnat2 (3) 3
mutations (3) 3
photoreceptors (3) 3
acetylcholine receptors (2) 2
adult (2) 2
aged (2) 2
blindness (2) 2
child (2) 2
child, preschool (2) 2
chromosome 8 (2) 2
chromosomes, human, pair 8 (2) 2
cngb3 (2) 2
cngb3 gene (2) 2
color vision defects - physiopathology (2) 2
cone degeneration (2) 2
deoxyribonucleic acid--dna (2) 2
dog diseases - genetics (2) 2
dogs (2) 2
gated cation channel (2) 2
genetics (2) 2
haplotypes (2) 2
ion channels - metabolism (2) 2
middle aged (2) 2
patients (2) 2
pingelapese (2) 2
polymorphism, restriction fragment length (2) 2
retinal cone photoreceptor cells - metabolism (2) 2
reverse transcriptase polymerase chain reaction (2) 2
achm3 gene (1) 1
achm3 locus (1) 1
acuity (1) 1
adenosine (1) 1
adolescent (1) 1
agriculture, dairy & animal science (1) 1
alleles (1) 1
amino acid sequence (1) 1
amino acid substitution - genetics (1) 1
basic medicine (1) 1
blotting, northern (1) 1
canine (1) 1
cation channel (1) 1
cercopithecus aethiops (1) 1
channel (1) 1
chromosome mapping (1) 1
chromosomes, artificial, yeast (1) 1
clonal deletion (1) 1
cloning (1) 1
cng channel (1) 1
cngb3 mutations (1) 1
codons (1) 1
color (1) 1
color perception tests (1) 1
color vision defects - ethnology (1) 1
color vision defects - veterinary (1) 1
colorblindness (1) 1
colour blindness (1) 1
complete achromatopsia (1) 1
cone (1) 1
congenital diseases (1) 1
contig mapping (1) 1
cos cells (1) 1
cyclic gmp (1) 1
cyclic nucleotide-gated channel (1) 1
dark adaptation (1) 1
day blindness (1) 1
dna (1) 1
dna mutational analysis - methods (1) 1
dna, complementary - metabolism (1) 1
dystrophy (1) 1
electroretinography (1) 1
exons (1) 1
family health (1) 1
frameshift mutation (1) 1
gated channel (1) 1
genes, recessive (1) 1
genetic heterogeneity (1) 1
genetic markers (1) 1
genetic research (1) 1
genotype (1) 1
more...
Language Language
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, 2005, Volume 13, Issue 3, pp. 302 - 308
Journal Article
Human Molecular Genetics, ISSN 0964-6906, 09/2000, Volume 9, Issue 14, pp. 2107 - 2116
Journal Article
No results were found for your search.

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