Homozygosity mapping and candidate prioritization identify mutations, missed by whole-exome sequencing, in SMOC2, causing major dental developmental defects
about
Mutation in SSUH2 Causes Autosomal-Dominant Dentin Dysplasia Type IA splicing mutation in VPS4B causes dentin dysplasia I.The etiology of cleft palate formation in BMP7-deficient mice.Canine Brachycephaly Is Associated with a Retrotransposon-Mediated Missplicing of SMOC2.Molars and incisors: show your microarray IDs.Identification of the causative gene for Simmental arachnomelia syndrome using a network-based disease gene prioritization approach.Mutations in the latent TGF-beta binding protein 3 (LTBP3) gene cause brachyolmia with amelogenesis imperfecta.EuFishBioMed (COST Action BM0804): a European network to promote the use of small fishes in biomedical research.Developmental disorders of the dentition: an update.Retinoic Acid Excess Impairs Amelogenesis Inducing Enamel Defects.Solving the molecular diagnostic testing conundrum for Mendelian disorders in the era of next-generation sequencing: single-gene, gene panel, or exome/genome sequencing.Genome-wide analysis of gene expression in human embryonic tooth germ.A morpholino-based screen to identify novel genes involved in craniofacial morphogenesis.The Gene Network Underlying Hypodontia.Odontoblasts: Specialized hard-tissue-forming cells in the dentin-pulp complex.Genetic Basis of Nonsyndromic and Syndromic Tooth Agenesis.Leveling the Playing Field in Homozygosity Mapping Using Map Distances.Deep sequencing reveals variations in somatic cell mosaic mutations between monozygotic twins with discordant psychiatric disease.Targeted Gene Panel Sequencing for Early-onset Inflammatory Bowel Disease and Chronic Diarrhea.Analysis of the canine brain transcriptome with an emphasis on the hypothalamus and cerebral cortex.A progeroid syndrome with neonatal presentation and long survival maps to 19p13.3p13.2.Smoc2 modulates embryonic myelopoiesis during zebrafish development.Overexpression of SMOC2 Attenuates the Tumorigenicity of Hepatocellular Carcinoma Cells and Is Associated With a Positive Postoperative Prognosis in Human Hepatocellular Carcinoma.The Biology Underlying Abnormalities of Tooth Number in Humans.The Changing Landscape in the Genetic Etiology of Human Tooth Agenesis.SMOC2 inhibits calcification of osteoprogenitor and endothelial cells.Whole exome sequencing identifies an AMBN missense mutation causing severe autosomal-dominant amelogenesis imperfecta and dentin disorders
P2860
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P2860
Homozygosity mapping and candidate prioritization identify mutations, missed by whole-exome sequencing, in SMOC2, causing major dental developmental defects
description
2011 nî lūn-bûn
@nan
2011 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2011 թվականի դեկտեմբերին հրատարակված գիտական հոդված
@hy
2011年の論文
@ja
2011年論文
@yue
2011年論文
@zh-hant
2011年論文
@zh-hk
2011年論文
@zh-mo
2011年論文
@zh-tw
2011年论文
@wuu
name
Homozygosity mapping and candi ...... r dental developmental defects
@ast
Homozygosity mapping and candi ...... r dental developmental defects
@en
Homozygosity mapping and candi ...... r dental developmental defects
@nl
type
label
Homozygosity mapping and candi ...... r dental developmental defects
@ast
Homozygosity mapping and candi ...... r dental developmental defects
@en
Homozygosity mapping and candi ...... r dental developmental defects
@nl
prefLabel
Homozygosity mapping and candi ...... r dental developmental defects
@ast
Homozygosity mapping and candi ...... r dental developmental defects
@en
Homozygosity mapping and candi ...... r dental developmental defects
@nl
P2093
P2860
P50
P1476
Homozygosity mapping and candi ...... r dental developmental defects
@en
P2093
Christelle Etard
Corinne Stoetzel
Jean-Pierre Strauss
Olivier Poch
Valérie Pelletier
Vincent Marion
Virginie Laugel
Véronique Geoffroy
Xavier Jamet
P2860
P304
P356
10.1016/J.AJHG.2011.11.002
P407
P577
2011-12-09T00:00:00Z