about
Homozygous nonsense mutation in the FOXE3 gene as a cause of congenital primary aphakia in humansTGFbeta2 knockout mice have multiple developmental defects that are non-overlapping with other TGFbeta knockout phenotypesProgenitor cells of the rod-free area centralis originate in the anterior dorsal optic vesicleA case of chorioretinal coloboma in a patient with achondroplasia.The Ultrastructural Localization of Type II, IV, and VI Collagens at the Vitreoretinal Interface.Neural crest derivatives in ocular development: discerning the eye of the stormEmerging functions of pannexin 1 in the eye.Embryologic and Fetal Development of the Human Eyelid.The zebrafish eye-a paradigm for investigating human ocular genetics.Modeling human retinal development with patient-specific induced pluripotent stem cells reveals multiple roles for visual system homeobox 2.Transcriptional regulatory network analysis during epithelial-mesenchymal transformation of retinal pigment epithelium.From bench to bedsideAchondroplasia and Macular Coloboma.Keratoplasty in congenital primary aphakia.Identification of a novel frameshift mutation in PAX6 gene and the clinical management in an Asian Indian aniridia family.
P2860
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P2860
description
1992 nî lūn-bûn
@nan
1992年の論文
@ja
1992年学术文章
@wuu
1992年学术文章
@zh-cn
1992年学术文章
@zh-hans
1992年学术文章
@zh-my
1992年学术文章
@zh-sg
1992年學術文章
@yue
1992年學術文章
@zh
1992年學術文章
@zh-hant
name
Embryology of the eye and its adnexae.
@ast
Embryology of the eye and its adnexae.
@en
type
label
Embryology of the eye and its adnexae.
@ast
Embryology of the eye and its adnexae.
@en
prefLabel
Embryology of the eye and its adnexae.
@ast
Embryology of the eye and its adnexae.
@en
P1476
Embryology of the eye and its adnexae.
@en
P2093
Barishak YR
P577
1992-01-01T00:00:00Z