Case of novel PITX2 gene mutation associated with Peters' anomaly and persistent hyperplastic primary vitreous.
about
pitx2 Deficiency results in abnormal ocular and craniofacial development in zebrafishChromosome abnormalities and the genetics of congenital corneal opacification.Absence of NR2E1 mutations in patients with aniridia.Genetics of anterior segment dysgenesis disorders.Studies of a pedigree with limbal dermoid cyst.Peters anomaly with post axial polydactyly, bilateral camptodactyly and club foot in a Kenyan neonate: a case report.PITX2 deficiency and associated human disease: insights from the zebrafish model.
P2860
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P2860
Case of novel PITX2 gene mutation associated with Peters' anomaly and persistent hyperplastic primary vitreous.
description
2009 nî lūn-bûn
@nan
2009年の論文
@ja
2009年学术文章
@wuu
2009年学术文章
@zh-cn
2009年学术文章
@zh-hans
2009年学术文章
@zh-my
2009年学术文章
@zh-sg
2009年學術文章
@yue
2009年學術文章
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2009年學術文章
@zh-hant
name
Case of novel PITX2 gene mutat ...... hyperplastic primary vitreous.
@en
Case of novel PITX2 gene mutat ...... hyperplastic primary vitreous.
@nl
type
label
Case of novel PITX2 gene mutat ...... hyperplastic primary vitreous.
@en
Case of novel PITX2 gene mutat ...... hyperplastic primary vitreous.
@nl
prefLabel
Case of novel PITX2 gene mutat ...... hyperplastic primary vitreous.
@en
Case of novel PITX2 gene mutat ...... hyperplastic primary vitreous.
@nl
P2093
P356
P1433
P1476
Case of novel PITX2 gene mutat ...... hyperplastic primary vitreous
@en
P2093
H Yoshikawa
K Ishikawa
T Ishibashi
P2888
P304
P356
10.1038/EYE.2009.114
P577
2009-05-22T00:00:00Z