Familial Axenfeld-Rieger anomaly, cardiac malformations, and sensorineural hearing loss: a provisionally unique genetic syndrome?
about
Analysis of RNA splicing defects in PITX2 mutants supports a gene dosage model of Axenfeld-Rieger syndrome.Functionally significant, rare transcription factor variants in tetralogy of Fallot.Glaucoma: genes, phenotypes, and new directions for therapy.Anaesthetic challenges in a patient with Axenfeld Rieger Syndrome.Xenopus: An emerging model for studying congenital heart disease.Lgr4 in ocular development and glaucomaIs primary open-angle glaucoma part of a generalized sensory neurodegeneration? A review of the evidence.Magnetic resonance imaging findings in Axenfeld-Rieger syndrome.Teratogenic effects of suramin on the chick embryo.Dental anomalies in Axenfeld-Rieger syndrome.
P2860
Q33249821-EEB82E85-6101-4044-8629-EBB78E979C99Q34004641-1ED15FAF-CED1-4C0E-A3B1-8B6D984B6B48Q34090204-A06B6ACA-1437-4891-AF65-6E6E72ABFA59Q34236625-9CE3AD5F-3F3E-41EE-B25E-114BA59B1F45Q35075360-1F1AA03B-EFE4-4372-BB69-358D3573B604Q36942765-1EF80668-F907-4B8B-84EE-06FEF94E1385Q38010766-9505255A-D7AA-4638-8D71-EFE0208453F6Q41107433-11453A58-E33B-4508-A5CC-0F4917596FF6Q44319881-D12B6B92-AB48-4D99-9A83-3B4505F8EEF3Q53611552-1CF98F7A-F961-4A06-AC54-FD4EA51D5894
P2860
Familial Axenfeld-Rieger anomaly, cardiac malformations, and sensorineural hearing loss: a provisionally unique genetic syndrome?
description
2002 nî lūn-bûn
@nan
2002 թուականի Օգոստոսին հրատարակուած գիտական յօդուած
@hyw
2002 թվականի օգոստոսին հրատարակված գիտական հոդված
@hy
2002年の論文
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2002年論文
@yue
2002年論文
@zh-hant
2002年論文
@zh-hk
2002年論文
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2002年論文
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2002年论文
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name
Familial Axenfeld-Rieger anoma ...... nally unique genetic syndrome?
@ast
Familial Axenfeld-Rieger anoma ...... nally unique genetic syndrome?
@en
type
label
Familial Axenfeld-Rieger anoma ...... nally unique genetic syndrome?
@ast
Familial Axenfeld-Rieger anoma ...... nally unique genetic syndrome?
@en
prefLabel
Familial Axenfeld-Rieger anoma ...... nally unique genetic syndrome?
@ast
Familial Axenfeld-Rieger anoma ...... nally unique genetic syndrome?
@en
P2093
P2860
P356
P1476
Familial Axenfeld-Rieger anoma ...... nally unique genetic syndrome?
@en
P2093
Balestri P
Farnetani MA
Vivarelli R
P2860
P304
P356
10.1002/AJMG.10493
P577
2002-08-01T00:00:00Z