dyskerin
Zinsser-Cole-Engman syndrome
utrophin
dyskaryotic
dysimmunity
titinopathy
pseudohypertrophic dystrophy
dystropathology
Duchenne's muscular dystrophy
dysontogenic
dyschromatoptic
homeolog
Nijmegen breakage syndrome
dysmorphogenetic
aarF
dysplasminogenemic
recessive
dystroglycanopathy
monomeric
Curschmann-Steinert disease
dysembryoplastic
protospacer
Steinert disease
domainome
dysferlinopathic
dyschromic
dystrophinopathic
myotonia atrophica
dysferlinopathy
Camurati-Engelmann disease
edit
X-linked recessive inheritance
pompholyx
dyskeratotic
dystrophia myotonica
congenital contractural arachnodactyly
dysmorphogenic
genus Genetta
idiochromatin
DiGeorge syndrome
Genetta
dyscephaly
chromosome mapping
chromoanasynthesis
mapping
Down's syndrome
dystrophia
XXY
pseudomale
genetic gap
dyshidrotic
dystrophinopathy
dyschondroplasic
dysontogenetic
cotransformant
hereditarian
mutable
aneupolyploid
McKusick-Kaufman syndrome
dyschromatic
nucleofilament
pseudochromosomal
acentric chromosome
whirlin
mutationistic
oculopharyngeal muscular dystrophy
Y-linked gene
genodermatose
genitocrural
dicentric
microduplication
Turner's syndrome
holandric gene
deoxyribonucleotide
pericentrosome
variation
zaspopathy
adermatoglyphia
Sry
acentric
unit character
monochromosomal
microdeletion
Edwards syndrome
sex chromosome
locus
replication fork
dominant
intrachromosomal
muscleblind
dinucleotidic
genecologic
insertion
hereditary hemorrhagic telangiectasia
biological father
diathesis
genotranscriptomic
trivalent
submetacentric

English words for 'A human gene, Dyskeratosis congenita 1, a small nucleolar ribonucleoprotein in which mutations are responsible for Zinsser-Cole-Engman syndrome.'

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