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(102 results)
Often used in the same context:
gene mutation,
mutation,
genetic defect,
mutant gene,
genetic abnormality,
gene,
genetic disorder,
recessive gene,
alleles,
genetically,
chromosome,
achromatopsia,
homozygous,
chromosomal anomaly,
phenotype,
myotonic dystrophy,
heritable,
herpes virus,
heterozygous,
haplotype,
mosaicism,
retrovirus,
bacterium,
enzyme,
genotype,
subtype,
herpesviruses,
abnormalities,
autosomal dominant disorder,
tumors,
penetrance,
degenerative disorder,
aneuploidy,
suppressor gene,
autosomal recessive disease,
medulloblastoma,
mutated,
toxoplasmosis,
autoantibodies,
homozygosity,
protein,
proband,
parasite,
monogenic,
methylation,
antibodies,
globin,
trypanosomes,
congenital disorder,
malaria parasite,
oncogene,
varicella zoster virus,
xeroderma pigmentosum,
motor neuron,
epigenetic,
polymorphism,
trypanosome,
lipin,
heterozygote,
mitochondrial,
dysgenesis,
parainfluenza virus,
mycobacterium tuberculosis,
nematode worm,
zebrafish,
polydactylism,
mycobacterium,
familial hypercholesterolemia,
hydrops,
hemochromatosis,
disease,
autoantibody,
karyotype,
gene expression,
galactosemia,
teratoma,
trisomy,
microcephaly,
genomes,
immunodeficiency,
blastomeres,
parasitic worm,
ectoderm,
mucins,
metabolic disorder,
adrenal cortex,
atopy,
herpes simplex virus,
poxvirus,
hypertrichosis,
acetylation,
malignancy,
toxoplasma,
borrelia burgdorferi,
nicotinamide,
eosinophilic,
neurofibroma,
bacteroides,
thyroid hormone,
prosopagnosia,
dpp,
melanocyte
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