Bardet-Biedl syndrome: Genetics, molecular pathophysiology, and disease management
about
Ophthalmic manifestations of endocrine disorders-endocrinology and the eye.Prescreening whole exome sequencing results from patients with retinal degeneration for variants in genes associated with retinal degeneration.Severe early onset obesity due to a novel missense mutation in exon 3 of leptin gene in an infant from Northwest India.
P2860
Bardet-Biedl syndrome: Genetics, molecular pathophysiology, and disease management
description
2016 nî lūn-bûn
@nan
2016 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած
@hyw
2016 թվականի սեպտեմբերին 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
Bardet-Biedl syndrome: Genetics, molecular pathophysiology, and disease management
@ast
Bardet-Biedl syndrome: Genetics, molecular pathophysiology, and disease management
@en
Bardet-Biedl syndrome: Genetics, molecular pathophysiology, and disease management
@nl
type
label
Bardet-Biedl syndrome: Genetics, molecular pathophysiology, and disease management
@ast
Bardet-Biedl syndrome: Genetics, molecular pathophysiology, and disease management
@en
Bardet-Biedl syndrome: Genetics, molecular pathophysiology, and disease management
@nl
prefLabel
Bardet-Biedl syndrome: Genetics, molecular pathophysiology, and disease management
@ast
Bardet-Biedl syndrome: Genetics, molecular pathophysiology, and disease management
@en
Bardet-Biedl syndrome: Genetics, molecular pathophysiology, and disease management
@nl
P2093
P2860
P3181
P356
P1476
Bardet-Biedl syndrome: Genetics, molecular pathophysiology, and disease management
@en
P2093
Parveen Sen
S Sripriya
Sathya Priya
Sheela Nampoothiri
P2860
P304
P3181
P356
10.4103/0301-4738.194328
P407
P5008
P577
2016-09-01T00:00:00Z