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(102 results)
Often used in the same context:
mutation,
genetic mutation,
gene mutation,
gene,
genetic defect,
recessive gene,
genetic abnormality,
heterozygous,
allele,
homozygous,
trypanosome,
phenotype,
haplotype,
chromosome,
retrovirus,
mitochondria,
mutated,
polymorphism,
mosaicism,
suppressor gene,
homozygosity,
autosomal recessive disease,
myotonic dystrophy,
constitutively,
globin,
dpp,
genetic,
enzyme,
epigenetic,
herpes virus,
blastomeres,
genotype,
protein,
messenger rna,
chimeric,
mutant,
aneuploidy,
autosomal dominant disorder,
achromatopsia,
melanocyte,
autoantibodies,
diploid,
transposon,
centrioles,
plasminogen,
overexpress,
herpesviruses,
lipin,
heritable,
gene expression,
lectin,
vasopressin,
herpesvirus,
mrna,
trypanosomes,
heterozygote,
nematode worm,
motor neuron,
monogenic,
oncogene,
neuropeptide,
entamoeba,
htlv,
peroxisome,
syngeneic,
proband,
homeobox gene,
polymerase,
myelination,
medulloblastoma,
mucins,
parthenogenetic,
polyploid,
xeroderma pigmentosum,
glycoproteins,
oncogenic,
autosomal,
rhesus,
arginase,
centromeres,
heterochromatin,
galactosemia,
protozoan,
plastid,
morphogen,
parainfluenza virus,
repressor,
neuroendocrine,
genetic disorder,
secretase,
cytidine,
methylation,
alanine,
antibodies,
nicotinamide,
acetylation,
nucleotide,
intron,
astrocyte,
valine,
cdna,
organelle
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