dyskerin
Zinsser-Cole-Engman syndrome
utrophin
dysimmunity
titinopathy
pseudohypertrophic dystrophy
dystropathology
Duchenne's muscular dystrophy
homeolog
Nijmegen breakage syndrome
aarF
recessive
dystroglycanopathy
Curschmann-Steinert disease
protospacer
Steinert disease
domainome
myotonia atrophica
dysferlinopathy
Camurati-Engelmann disease
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X-linked recessive inheritance
pompholyx
dystrophia myotonica
congenital contractural arachnodactyly
genus Genetta
idiochromatin
DiGeorge syndrome
Genetta
dyscephaly
chromosome mapping
chromoanasynthesis
mapping
dystrophia
pseudomale
genetic gap
dystrophinopathy
cotransformant
aneupolyploid
McKusick-Kaufman syndrome
nucleofilament
acentric chromosome
whirlin
oculopharyngeal muscular dystrophy
Y-linked gene
microduplication
Turner's syndrome
holandric gene
deoxyribonucleotide
pericentrosome
variation
zaspopathy
adermatoglyphia
acentric
unit character
microdeletion
Edwards syndrome
sex chromosome
locus
replication fork
dominant
muscleblind
insertion
hereditary hemorrhagic telangiectasia
biological father
diathesis
trivalent