Chromosome 18q22.2-->qter deletion and a congenital anomaly syndrome with multiple vertebral segmentation defects
about
A gene for autosomal recessive spondylocostal dysostosis maps to 19q13.1-q13.3Novel mutations in DLL3, a somitogenesis gene encoding a ligand for the Notch signalling pathway, cause a consistent pattern of abnormal vertebral segmentation in spondylocostal dysostosisHigh-resolution genome screen for bone mineral density in heterogeneous stock rat.VACTERL Association Etiology: The Impact of de novo and Rare Copy Number VariationsFive known tagging DLL3 SNPs are not associated with congenital scoliosis: A case-control association study in a Chinese Han population.SOCS6 is a selective suppressor of receptor tyrosine kinase signaling.
P2860
Chromosome 18q22.2-->qter deletion and a congenital anomaly syndrome with multiple vertebral segmentation defects
description
1997 nî lūn-bûn
@nan
1997 թուականի Մայիսին հրատարակուած գիտական յօդուած
@hyw
1997 թվականի մայիսին 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
Chromosome 18q22.2-->qter dele ...... vertebral segmentation defects
@ast
Chromosome 18q22.2-->qter dele ...... vertebral segmentation defects
@en
type
label
Chromosome 18q22.2-->qter dele ...... vertebral segmentation defects
@ast
Chromosome 18q22.2-->qter dele ...... vertebral segmentation defects
@en
prefLabel
Chromosome 18q22.2-->qter dele ...... vertebral segmentation defects
@ast
Chromosome 18q22.2-->qter dele ...... vertebral segmentation defects
@en
P2093
P2860
P356
P1476
Chromosome 18q22.2-->qter dele ...... vertebral segmentation defects
@en
P2093
M S Watson
V Sheen-Kaniecki
P2860
P304
P356
10.1136/JMG.34.5.414
P407
P577
1997-05-01T00:00:00Z