about
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
Q27308985-EC795C16-EFCD-4EA6-83F8-4DDCF972AE6EQ34800084-4364DF28-0A99-4A4C-A26C-8F76F5EA6B95Q37180921-2F484554-6E34-468D-A882-6FD979AEC45DQ37184616-D186857C-5A03-4418-8C98-E8348670A78DQ38803469-22513FA3-5B7B-48BA-BAC7-F5ADB5F030F9Q41221199-56D618A8-FF1A-4670-9F7B-E250C3989C61Q48318063-5C63DA59-2DA6-48B2-B5CB-DC2AEC59E2A8Q53066942-96B1A263-7468-4BDF-AA23-3AAADA1BF0B5
P2860
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
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2011年學術文章
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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
P2860
P1433
P1476
PRRX1 is mutated in a fetus with agnathia-otocephaly.
@en
P2093
D Kamnasaran
P2860
P304
P356
10.1111/J.1399-0004.2010.01531.X
P577
2011-03-01T00:00:00Z