Linkage analysis in blepharophimosis-ptosis syndrome confirms localisation to 3q21-24
about
FOXL2 and BPES: mutational hotspots, phenotypic variability, and revision of the genotype-phenotype correlationA novel case of unilateral blepharophimosis syndrome and mental retardation associated with de novo trisomy for chromosome 3qOvarian differentiation and gonadal failure.Genetic analysis of the FOXL2 gene using quantitative real-time PCR in Chinese patients with blepharophimosis-ptosis-epicanthus inversus syndromeA gene for isolated congenital ptosis maps to a 3-cM region within 1p32-p34.1.Blepharophimosis: a causally heterogeneous malformation frequently associated with developmental disabilities.
P2860
Linkage analysis in blepharophimosis-ptosis syndrome confirms localisation to 3q21-24
description
1995 nî lūn-bûn
@nan
1995 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած
@hyw
1995 թվականի հոտեմբերին հրատարակված գիտական հոդված
@hy
1995年の論文
@ja
1995年論文
@yue
1995年論文
@zh-hant
1995年論文
@zh-hk
1995年論文
@zh-mo
1995年論文
@zh-tw
1995年论文
@wuu
name
Linkage analysis in blepharophimosis-ptosis syndrome confirms localisation to 3q21-24
@ast
Linkage analysis in blepharophimosis-ptosis syndrome confirms localisation to 3q21-24
@en
type
label
Linkage analysis in blepharophimosis-ptosis syndrome confirms localisation to 3q21-24
@ast
Linkage analysis in blepharophimosis-ptosis syndrome confirms localisation to 3q21-24
@en
prefLabel
Linkage analysis in blepharophimosis-ptosis syndrome confirms localisation to 3q21-24
@ast
Linkage analysis in blepharophimosis-ptosis syndrome confirms localisation to 3q21-24
@en
P2093
P2860
P356
P1476
Linkage analysis in blepharophimosis-ptosis syndrome confirms localisation to 3q21-24
@en
P2093
P2860
P304
P356
10.1136/JMG.32.10.774
P407
P577
1995-10-01T00:00:00Z