Molecular and Clinical Findings in Patients With Knobloch Syndrome.
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Detailed Clinical Phenotype and Molecular Genetic Findings in CLN3-Associated Isolated Retinal Degeneration.Optical coherence tomography findings and successful repair of retina detachment in Knobloch syndrome.Knobloch syndrome associated with Polymicrogyria and early onset of retinal detachment: two case reports.Molecular Genetics of Pigment Dispersion Syndrome and Pigmentary Glaucoma: New Insights into Mechanisms.Knobloch syndrome caused by homozygous frameshift mutation of the COL18A1 gene in a Chinese pedigree.
P2860
Molecular and Clinical Findings in Patients With Knobloch Syndrome.
description
2016 nî lūn-bûn
@nan
2016 թուականի Մայիսին հրատարակուած գիտական յօդուած
@hyw
2016 թվականի մայիսին հրատարակված գիտական հոդված
@hy
2016年の論文
@ja
2016年学术文章
@wuu
2016年学术文章
@zh-cn
2016年学术文章
@zh-hans
2016年学术文章
@zh-my
2016年学术文章
@zh-sg
2016年學術文章
@yue
name
Molecular and Clinical Findings in Patients With Knobloch Syndrome.
@ast
Molecular and Clinical Findings in Patients With Knobloch Syndrome.
@en
Molecular and Clinical Findings in Patients With Knobloch Syndrome.
@nl
type
label
Molecular and Clinical Findings in Patients With Knobloch Syndrome.
@ast
Molecular and Clinical Findings in Patients With Knobloch Syndrome.
@en
Molecular and Clinical Findings in Patients With Knobloch Syndrome.
@nl
prefLabel
Molecular and Clinical Findings in Patients With Knobloch Syndrome.
@ast
Molecular and Clinical Findings in Patients With Knobloch Syndrome.
@en
Molecular and Clinical Findings in Patients With Knobloch Syndrome.
@nl
P2093
P1433
P1476
Molecular and Clinical Findings in Patients With Knobloch Syndrome
@en
P2093
Aman Chandra
Andrew R Webster
Anthony T Moore
Cristy A Ku
Gavin Arno
Graham E Holder
Indran Davagnanam
Mark E Pennesi
Michel Michaelides
Naushin Waseem
P304
P356
10.1001/JAMAOPHTHALMOL.2016.1073
P407
P50
P577
2016-07-01T00:00:00Z