Retinal vasculopathy in a family with autosomal dominant dyskeratosis congenita.
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Ocular manifestations of idiopathic aplastic anemia: retrospective study and literature review.Bilateral Proliferative Retinopathy Associated With Hoyeraal-Hreidarsson Syndrome, a Severe Form of Dyskeratosis Congenita.Ocular involvement in primary immunodeficiency diseases.Retinal findings and a novel TINF2 mutation in Revesz syndrome: Clinical and molecular correlations with pediatric retinal vasculopathies.Unilateral Coats'-like disease and an intragenic deletion in the TERC gene: A case report.
P2860
Retinal vasculopathy in a family with autosomal dominant dyskeratosis congenita.
description
2009 nî lūn-bûn
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2009年の論文
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2009年学术文章
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2009年学术文章
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2009年学术文章
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2009年学术文章
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2009年学术文章
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2009年学术文章
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2009年學術文章
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name
Retinal vasculopathy in a family with autosomal dominant dyskeratosis congenita.
@en
Retinal vasculopathy in a family with autosomal dominant dyskeratosis congenita.
@nl
type
label
Retinal vasculopathy in a family with autosomal dominant dyskeratosis congenita.
@en
Retinal vasculopathy in a family with autosomal dominant dyskeratosis congenita.
@nl
prefLabel
Retinal vasculopathy in a family with autosomal dominant dyskeratosis congenita.
@en
Retinal vasculopathy in a family with autosomal dominant dyskeratosis congenita.
@nl
P2093
P2860
P1433
P1476
Retinal vasculopathy in a family with autosomal dominant dyskeratosis congenita.
@en
P2093
Charles A Johnson
Jose S Pulido
Mark Hatfield
P2860
P304
P356
10.3109/13816810903148012
P577
2009-12-01T00:00:00Z