Mutations in the T (brachyury) gene cause a novel syndrome consisting of sacral agenesis, abnormal ossification of the vertebral bodies and a persistent notochordal canal
about
The T-box gene family: emerging roles in development, stem cells and cancerThe mammalian cervical vertebrae blueprint depends on the T (brachyury) gene.Paleodysmorphology and paleoteratology: Diagnosing and interpreting congenital conditions of the skeleton in anthropological contexts.Prenatal Evidence of Persistent Notochord and Absent Sacrum Caused by a Mutation in the T (Brachyury) Gene.Persistent Notochord in a Fetus with COL2A1 Mutation.Autosomal recessive variations of TBX6, from congenital scoliosis to spondylocostal dysostosis.Symptomatic lower urinary tract dysfunction in sacral agenesis: Potentially high risk?Key apoptotic genes APAF1 and CASP9 implicated in recurrent folate-resistant neural tube defects.Heterozygous mutations in the T (brachyury) gene.
P2860
Q27000341-42B8C57A-2996-49B1-8CDE-67F5A1292CDFQ35145769-45D12815-10D7-4433-85ED-EDB4C02FA9ADQ36111018-3CCC991D-FC31-445C-87FE-70FB1535397FQ37571458-E0BA25A1-FF76-4FE7-8541-A8563E733746Q38599046-5A6E9B9F-6EA3-4998-9584-5008C6F4FEF4Q39175747-0FFDDAAA-CF9D-4AB1-8778-29C2DEC73481Q49371069-2ED34120-B6EB-4C96-AA00-EC24DCC67B65Q49865560-7271C1C4-E79E-4CB6-8486-AB56FA5B6834Q50687244-832DBF8C-4350-4063-97F7-EC7FA15BEE6C
P2860
Mutations in the T (brachyury) gene cause a novel syndrome consisting of sacral agenesis, abnormal ossification of the vertebral bodies and a persistent notochordal canal
description
2014 nî lūn-bûn
@nan
2014 թուականի Փետրուարին հրատարակուած գիտական յօդուած
@hyw
2014 թվականի փետրվարին հրատարակված գիտական հոդված
@hy
2014年の論文
@ja
2014年論文
@yue
2014年論文
@zh-hant
2014年論文
@zh-hk
2014年論文
@zh-mo
2014年論文
@zh-tw
2014年论文
@wuu
name
Mutations in the T (brachyury) ...... a persistent notochordal canal
@ast
Mutations in the T (brachyury) ...... a persistent notochordal canal
@en
Mutations in the T (brachyury) ...... a persistent notochordal canal
@en-gb
Mutations in the T (brachyury) ...... a persistent notochordal canal
@nl
type
label
Mutations in the T (brachyury) ...... a persistent notochordal canal
@ast
Mutations in the T (brachyury) ...... a persistent notochordal canal
@en
Mutations in the T (brachyury) ...... a persistent notochordal canal
@en-gb
Mutations in the T (brachyury) ...... a persistent notochordal canal
@nl
prefLabel
Mutations in the T (brachyury) ...... a persistent notochordal canal
@ast
Mutations in the T (brachyury) ...... a persistent notochordal canal
@en
Mutations in the T (brachyury) ...... a persistent notochordal canal
@en-gb
Mutations in the T (brachyury) ...... a persistent notochordal canal
@nl
P2093
P2860
P50
P1476
Mutations in the T (brachyury) ...... a persistent notochordal canal
@en
P2093
A F M Moorman
C M Bilardo
M C van Maarle
M M A M Mannens
P2860
P356
10.1136/JMEDGENET-2013-102001
P407
P577
2014-02-01T00:00:00Z