about
Ring chromosome 18 in combination with 18q12.1 (DTNA) interstitial microdeletion in a patient with multiple congenital defects.Congenital cataract, facial dysmorphism and demyelinating neuropathy (CCFDN) in 10 Czech Gypsy children--frequent and underestimated cause of disability among Czech Gypsies.Carboxy-terminal domain phosphatase 1 silencing results in the inhibition of tumor formation ability in gastric cancer cells.Carrier rates of four single-gene disorders in Croatian Bayash Roma.A case of congenital cataracts, facial dysmorphisms, neuropathy, and hyperkinetic movement disorder.Phenotype-genotype correlations in patients with Marinesco-Sjögren syndrome.
P2860
description
2006 nî lūn-bûn
@nan
2006 թուականի Օգոստոսին հրատարակուած գիտական յօդուած
@hyw
2006 թվականի օգոստոսին հրատարակված գիտական հոդված
@hy
2006年の論文
@ja
2006年論文
@yue
2006年論文
@zh-hant
2006年論文
@zh-hk
2006年論文
@zh-mo
2006年論文
@zh-tw
2006年论文
@wuu
name
Congenital cataracts-facial dysmorphism-neuropathy
@ast
Congenital cataracts-facial dysmorphism-neuropathy
@en
Congenital cataracts-facial dysmorphism-neuropathy
@en-gb
Congenital cataracts-facial dysmorphism-neuropathy
@nl
type
label
Congenital cataracts-facial dysmorphism-neuropathy
@ast
Congenital cataracts-facial dysmorphism-neuropathy
@en
Congenital cataracts-facial dysmorphism-neuropathy
@en-gb
Congenital cataracts-facial dysmorphism-neuropathy
@nl
prefLabel
Congenital cataracts-facial dysmorphism-neuropathy
@ast
Congenital cataracts-facial dysmorphism-neuropathy
@en
Congenital cataracts-facial dysmorphism-neuropathy
@en-gb
Congenital cataracts-facial dysmorphism-neuropathy
@nl
P2860
P921
P356
P1476
Congenital cataracts-facial dysmorphism-neuropathy
@en
P2093
Luba Kalaydjieva
P2860
P2888
P356
10.1186/1750-1172-1-32
P407
P5008
P577
2006-08-29T00:00:00Z
P5875
P6179
1021163757