Genome-wide linkage analysis and mutation analysis of hereditary congenital blepharoptosis in a Japanese family.
about
ZFHX4 interacts with the NuRD core member CHD4 and regulates the glioblastoma tumor-initiating cell stateCharacterization of a 8q21.11 microdeletion syndrome associated with intellectual disability and a recognizable phenotype.Controversies and advances in the management of congenital ptosis.Whole-exome sequencing to identify novel mutations of nevoid basal cell carcinoma syndrome in a Chinese population.8q21.11 microdeletion in two patients with syndromic peters anomaly.Ptosis in childhood: A clinical sign of several disorders: Case series reports and literature review
P2860
Genome-wide linkage analysis and mutation analysis of hereditary congenital blepharoptosis in a Japanese family.
description
2007 nî lūn-bûn
@nan
2007年の論文
@ja
2007年学术文章
@wuu
2007年学术文章
@zh
2007年学术文章
@zh-cn
2007年学术文章
@zh-hans
2007年学术文章
@zh-my
2007年学术文章
@zh-sg
2007年學術文章
@yue
2007年學術文章
@zh-hant
name
Genome-wide linkage analysis a ...... roptosis in a Japanese family.
@en
Genome-wide linkage analysis a ...... roptosis in a Japanese family.
@nl
type
label
Genome-wide linkage analysis a ...... roptosis in a Japanese family.
@en
Genome-wide linkage analysis a ...... roptosis in a Japanese family.
@nl
prefLabel
Genome-wide linkage analysis a ...... roptosis in a Japanese family.
@en
Genome-wide linkage analysis a ...... roptosis in a Japanese family.
@nl
P2093
P1476
Genome-wide linkage analysis a ...... roptosis in a Japanese family.
@en
P2093
Akiyoshi Hirano
Koh-Ichiro Yoshiura
Mitsuko Nakashima
Motoi Nakano
Nobutomo Miwa
Norio Niikawa
Shinji Kondoh
Tatsuya Kishino
P2860
P2888
P356
10.1007/S10038-007-0214-6
P577
2007-11-07T00:00:00Z