about
Cornelia de Lange syndrome with NIPBL mutation and mosaic Turner syndrome in the same individual.Chromosome abnormalities and the genetics of congenital corneal opacification.The eye as a window to rare endocrine disorders.The presence of eye defects in patients with Turner syndrome is irrespective of their karyotype.Axenfeld-Rieger spectrum in a patient with 45,X Turner syndrome.A heterozygous mutation in RPGR associated with X-linked retinitis pigmentosa in a patient with Turner syndrome mosaicism (45,X/46,XX).The occurrence of ocular diseases in patients with Turner syndrome
P2860
Q34296411-391CE69F-B411-4F39-AE33-0B2B0404563BQ35068028-987E0EAE-10E7-4D54-B003-C4219359A59FQ38013120-BA863A76-BE80-4662-A153-DA3BBEED3DFCQ41075860-EC2310A2-D4F7-49DF-88D0-A44FE26F2642Q46330744-2241049C-D80A-4080-899D-E0E2859B6909Q52786879-C306B1D8-9CA2-4B08-90CE-05B4672E9AB0Q58024988-196E8B68-B37E-41BE-9C0F-C46B8497CE86
P2860
description
1997 nî lūn-bûn
@nan
1997 թուականի Օգոստոսին հրատարակուած գիտական յօդուած
@hyw
1997 թվականի օգոստոսին հրատարակված գիտական հոդված
@hy
1997年の論文
@ja
1997年論文
@yue
1997年論文
@zh-hant
1997年論文
@zh-hk
1997年論文
@zh-mo
1997年論文
@zh-tw
1997年论文
@wuu
name
Anterior segment dysgenesis in mosaic Turner syndrome
@ast
Anterior segment dysgenesis in mosaic Turner syndrome
@en
type
label
Anterior segment dysgenesis in mosaic Turner syndrome
@ast
Anterior segment dysgenesis in mosaic Turner syndrome
@en
prefLabel
Anterior segment dysgenesis in mosaic Turner syndrome
@ast
Anterior segment dysgenesis in mosaic Turner syndrome
@en
P2093
P2860
P356
P1476
Anterior segment dysgenesis in mosaic Turner syndrome
@en
P2093
Clayton-Smith J
Ridgway AE
P2860
P304
P356
10.1136/BJO.81.8.639
P407
P577
1997-08-01T00:00:00Z