PRRX1 is mutated in a fetus with agnathia-otocephaly.

PRRX1 is mutated in a fetus with agnathia-otocephaly.

Item
http://www.wikidata.org/entity/Q51889592
Competition between Jagged-Notch and Endothelin1 Signaling Selectively Restricts Cartilage Formation in the Zebrafish Upper FaceA mouse splice-site mutant and individuals with atypical chromosome 22q11.2 deletions demonstrate the crucial role for crkl in craniofacial and pharyngeal development.Otocephaly-Dysgnathia Complex: Description of Four Cases and Confirmation of the Role of OTX2Prenatal Diagnosis of Isolated Agnathia-Otocephaly: A Case Report and Review of the LiteratureTranscriptional control of chondrocyte specification and differentiation.Intercellular Genetic Interaction Between Irf6 and Twist1 during Craniofacial Development.Chromosomal Imbalances in Patients with Congenital Cardiac Defects: A Meta-analysis Reveals Novel Potential Critical Regions Involved in Heart Development.Mandibular dysostosis without microphthalmia caused by OTX2 deletion.
P2860

PRRX1 is mutated in a fetus with agnathia-otocephaly.

Item
http://www.wikidata.org/entity/Q51889592
description
2011 nî lūn-bûn
@nan
2011年の論文
@ja
2011年学术文章
@wuu
2011年学术文章
@zh
2011年学术文章
@zh-cn
2011年学术文章
@zh-hans
2011年学术文章
@zh-my
2011年学术文章
@zh-sg
2011年學術文章
@yue
2011年學術文章
@zh-hant
name
PRRX1 is mutated in a fetus with agnathia-otocephaly.
@en
PRRX1 is mutated in a fetus with agnathia-otocephaly.
@nl
type
label
PRRX1 is mutated in a fetus with agnathia-otocephaly.
@en
PRRX1 is mutated in a fetus with agnathia-otocephaly.
@nl
prefLabel
PRRX1 is mutated in a fetus with agnathia-otocephaly.
@en
PRRX1 is mutated in a fetus with agnathia-otocephaly.
@nl
P1433
P1476
P2093
P2860
P304
P31
P356
P433
P478
P50
P577
P698
P356
P1433
P1476
PRRX1 is mutated in a fetus with agnathia-otocephaly.
@en
P2093
P2860
P304
P31
P356
10.1111/J.1399-0004.2010.01531.X
P433
P478
P50
P577
P698