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1
Genetics for ENT Specialists: The Molecular Genetic Basis of ENT Disorders
Remedica Publishing
Dirk Kunst
,
Hannie Kremer
,
Cor Cremers
syndrome
gene
mutations
mutation
hearing
patients
qxd
complete3
p480
impairment
snhi
diagnosis
inheritance
genes
autosomal
genetics
dna
features
figure
clinical
onset
inherited
protein
cases
specialists
spectrum
effect
chromosome
counseling
analysis
chromosomal
vestibular
mitochondrial
recessive
reported
mutational
affected
severe
congenital
unknown
epidemiology
phenotype
frequencies
progressive
symptoms
diseases
linked
deletions
abnormalities
chromosomes
年:
2004
語言:
english
文件:
PDF, 1.35 MB
你的標籤:
0
/
0
english, 2004
2
The memoirs of Lady Hyegyŏng: the autobiographical writings of a Crown Princess of eighteenth century Korea
University of California Press
Hyegyŏnggung Hong Ssi
,
JaHyun Kim Haboush
prince
majesty
sado
hong
heir
royal
palace
chngjo
yngjo
hyegyng
minister
crown
filial
memoir
chng
princess
uncle
memorial
devotion
snhi
kugyng
affection
madame
hugym
ponghan
kwiju
dowager
mourning
deeply
pavilion
incident
throne
residence
sillok
highness
memoirs
grandfather
older
sagacious
maternal
officials
regency
served
grief
manuscript
ladies
tears
marriage
examination
ceremony
年:
1996
語言:
english
文件:
EPUB, 2.55 MB
你的標籤:
0
/
0
english, 1996
3
Memoirs Of A Korean Queen
Routledge
Hong
prince
royal
crown
palace
grandson
yngjo
snhi
princess
mansion
favour
filial
incident
unable
whenever
affection
dowager
wedding
dang
loved
gate
chngjo
council
maids
worried
behaviour
board
officials
treated
chng
chngsng
governess
pavilion
shrine
wept
upset
extremely
madame
mourning
examination
hwap
duty
grief
serious
sorrow
tears
funeral
highness
inwn
record
palanquin
年:
2013
語言:
english
文件:
EPUB, 1.59 MB
你的標籤:
0
/
5.0
english, 2013
4
Genetic Hearing Impairment: Its Clinical Presentations (Advances in Otorhinolaryngology, Vol. 61)
S Karger Pub
C.W.R.J.
,
Ed. Cremers
hearing
deafness
gene
syndrome
mutation
mutations
impairment
genet
patients
cremers
clinical
affected
autosomal
vestibular
hum
individuals
recessive
sensorineural
nonsyndromic
function
genes
phenotype
locus
analysis
usher
deaf
khz
chromosome
syndromic
progressive
linked
frequency
huygen
myosin
profound
mitochondrial
hereditary
identified
cases
rjh
connexin
congenital
frequencies
severe
onset
features
pendred
reported
stickler
threshold
年:
2002
語言:
english
文件:
PDF, 4.33 MB
你的標籤:
0
/
0
english, 2002
5
Grumpy Billionaire Cowboy
Willow Finn
hiw
zeke
agd
yob
zoe
hiah
carriage
hso
sno
thst
zhe
desk
uaz
yog
beach
ghe
kgh
akogh
dudnht
a’ogt
fe.t
nlw
kwwg
cyao
garah
qhe
cvd
ugth
wuth
conversation
haie
jyt
ogt
snhi
wcl
breakfast
dndgvh
ios
lmwae
ride
uhat
iog.d
jeen
keme
logxd
ohe
saghwd
siy
sogxd
wasnht
語言:
english
文件:
PDF, 450 KB
你的標籤:
0
/
0
english
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