1192t
1445t
autosomal
consanguinity
deafness
disclosed
dysphagia
dystrophy
ectodermal
enamel
exome
grainyhead
haploinsufficiency
homozygous
hyperpigmentation
hypodontia
hypoplasia
ile482lys
immortalized
junctions
keratoderma
kuwaiti
lifelong
nail
palmoplantar
recessive
sensorineural
transcriptomic
tyr398his
|